Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 29969 |
|---|---|
| ensemblid | ENSG00000135272.13 |
| hgncid | 28870 |
| symbol | MDFIC |
| name | MyoD family inhibitor domain containing |
| refseq_nuc | NM_001166345.3 |
| refseq_prot | NP_001159817.1 |
| ensembl_nuc | ENST00000393486.6 |
| ensembl_prot | ENSP00000377126.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 114922094 |
| end | 115019917 |
| strand | + |
| ver | v1.2 |
| region | chr7:114922094-115019917 |
| region5000 | chr7:114917094-115024917 |
| regionname0 | MDFIC_chr7_114922094_115019917 |
| regionname5000 | MDFIC_chr7_114917094_115024917 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 246 | 332 | 77 | 68 | 136 | 13 | 36 | 100 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0002 | 0/0 | 246 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0003 | 0/0 | 246 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 741 | 321 | 70 | 68 | 134 | 13 | 35 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| c0002 | 1/0 | 741 | 5 | 4 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| c0003 | 0/0 | 741 | 3 | 3 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| c0004 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| c0005 | 0/0 | 741 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| c0006 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| c0007 | 0/0 | 741 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| c0008 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4633 | 52 | 8 | 1 | 38 | 0 | 5 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0002 | 0/0 | 4637 | 37 | 21 | 8 | 0 | 1 | 7 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0003 | 0/0 | 4637 | 22 | 3 | 8 | 7 | 2 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0004 | 0/0 | 4638 | 21 | 0 | 4 | 12 | 3 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0005 | 0/0 | 4636 | 20 | 2 | 6 | 11 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0006 | 0/0 | 4642 | 14 | 0 | 0 | 14 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0007 | 0/0 | 4633 | 13 | 1 | 9 | 0 | 2 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0008 | 0/0 | 4633 | 10 | 5 | 3 | 0 | 2 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0009 | 0/0 | 4637 | 10 | 2 | 8 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0010 | 0/0 | 4637 | 9 | 3 | 0 | 4 | 1 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0011 | 0/0 | 4637 | 9 | 3 | 0 | 2 | 0 | 4 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0012 | 0/0 | 4633 | 8 | 3 | 3 | 0 | 2 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0013 | 0/0 | 4633 | 8 | 0 | 0 | 8 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0014 | 0/0 | 4629 | 7 | 0 | 0 | 7 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0015 | 0/0 | 4632 | 7 | 0 | 2 | 5 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0016 | 0/0 | 4634 | 7 | 0 | 1 | 6 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0017 | 1/0 | 4633 | 5 | 0 | 2 | 1 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0018 | 0/0 | 4641 | 5 | 0 | 0 | 4 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0019 | 0/0 | 4625 | 4 | 3 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0020 | 0/0 | 4638 | 4 | 0 | 4 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0021 | 0/0 | 4640 | 4 | 0 | 0 | 4 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0022 | 0/0 | 4625 | 3 | 3 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0023 | 0/1 | 4641 | 3 | 2 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0024 | 0/0 | 4644 | 3 | 0 | 1 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0025 | 0/0 | 4633 | 3 | 0 | 2 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0026 | 0/0 | 4633 | 3 | 0 | 0 | 2 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0027 | 0/0 | 4637 | 2 | 2 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0028 | 0/0 | 4638 | 2 | 0 | 0 | 0 | 0 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0029 | 0/0 | 4642 | 2 | 0 | 0 | 0 | 0 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0030 | 0/0 | 4645 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0031 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0032 | 0/0 | 4633 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0033 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0034 | 0/0 | 4633 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0035 | 0/0 | 4637 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0036 | 0/0 | 4633 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0037 | 0/0 | 4633 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0038 | 0/0 | 4636 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0039 | 0/0 | 4634 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0040 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0041 | 0/0 | 4633 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0042 | 0/0 | 4633 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0043 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0044 | 0/0 | 4633 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0045 | 0/0 | 4634 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0046 | 0/0 | 4633 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0047 | 0/0 | 4637 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0048 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0049 | 0/0 | 4637 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0050 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0051 | 0/0 | 4644 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0052 | 0/0 | 4645 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0053 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0054 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0055 | 0/0 | 4649 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0056 | 0/0 | 4636 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0057 | 0/0 | 4637 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0058 | 0/0 | 4633 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0059 | 0/0 | 4633 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0060 | 0/0 | 4633 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0061 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0062 | 0/0 | 4609 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0063 | 0/0 | 4625 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0064 | 0/0 | 4637 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| t0065 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0014 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0021 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 741 | 321 | 70 | 68 | 134 | 13 | 35 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0002 | 1/0 | 741 | 5 | 4 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0003 | 0/0 | 741 | 3 | 3 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0006 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0007 | 0/0 | 741 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0008 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0002c0004 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0003c0005 | 0/0 | 741 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5373 | 50 | 8 | 1 | 36 | 0 | 5 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0002 | 0/0 | 5377 | 35 | 19 | 8 | 0 | 1 | 7 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0003 | 0/0 | 5377 | 22 | 3 | 8 | 7 | 2 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0004 | 0/0 | 5378 | 21 | 0 | 4 | 12 | 3 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0005 | 0/0 | 5376 | 19 | 2 | 6 | 11 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0006 | 0/0 | 5382 | 14 | 0 | 0 | 14 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0007 | 0/0 | 5373 | 13 | 1 | 9 | 0 | 2 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0008 | 0/0 | 5373 | 9 | 4 | 3 | 0 | 2 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0009 | 0/0 | 5377 | 10 | 2 | 8 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0010 | 0/0 | 5377 | 9 | 3 | 0 | 4 | 1 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0011 | 0/0 | 5377 | 9 | 3 | 0 | 2 | 0 | 4 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0012 | 0/0 | 5373 | 6 | 2 | 3 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0013 | 0/0 | 5373 | 8 | 0 | 0 | 8 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0014 | 0/0 | 5369 | 7 | 0 | 0 | 7 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0015 | 0/0 | 5372 | 7 | 0 | 2 | 5 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0016 | 0/0 | 5374 | 7 | 0 | 1 | 6 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0017 | 0/0 | 5373 | 4 | 0 | 2 | 1 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0018 | 0/0 | 5381 | 5 | 0 | 0 | 4 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0019 | 0/0 | 5365 | 4 | 3 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0020 | 0/0 | 5378 | 4 | 0 | 4 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0021 | 0/0 | 5380 | 4 | 0 | 0 | 4 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0022 | 0/0 | 5365 | 3 | 3 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0023 | 0/1 | 5381 | 2 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0024 | 0/0 | 5384 | 3 | 0 | 1 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0025 | 0/0 | 5373 | 3 | 0 | 2 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0026 | 0/0 | 5373 | 3 | 0 | 0 | 2 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0027 | 0/0 | 5377 | 2 | 2 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0028 | 0/0 | 5378 | 2 | 0 | 0 | 0 | 0 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0029 | 0/0 | 5382 | 2 | 0 | 0 | 0 | 0 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0030 | 0/0 | 5385 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0032 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0033 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0034 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0035 | 0/0 | 5377 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0037 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0038 | 0/0 | 5376 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0039 | 0/0 | 5374 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0040 | 0/0 | 5349 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0041 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0042 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0044 | 0/0 | 5373 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0045 | 0/0 | 5374 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0046 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0047 | 0/0 | 5377 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0048 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0049 | 0/0 | 5377 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0050 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0051 | 0/0 | 5384 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0052 | 0/0 | 5385 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0053 | 0/0 | 5385 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0054 | 0/0 | 5386 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0055 | 0/0 | 5389 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0056 | 0/0 | 5376 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0057 | 0/0 | 5377 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0058 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0059 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0060 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0061 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0062 | 0/0 | 5349 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0063 | 0/0 | 5365 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0064 | 0/0 | 5377 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0001t0065 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0002t0002 | 0/0 | 5377 | 2 | 2 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0002t0012 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0002t0017 | 1/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0002t0023 | 0/0 | 5381 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0003t0031 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0003t0036 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0003t0043 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0006t0001 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0007t0005 | 0/0 | 5376 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0001c0008t0001 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0002c0004t0008 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| a0003c0005t0012 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | copy fasta | chr7 | 114917094 | 115024917 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0007g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0007g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0007g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0007g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0007g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0008g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0008g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0008g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0009g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0009g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0009g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0009g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0009g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0009g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0010g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0010g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0010g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0010g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0010g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0010g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0011g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0011g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0011g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0011g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0011g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0011g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0012g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0012g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0012g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0012g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0012g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0013g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0013g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0013g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0013g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0013g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0013g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0013g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0014g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0014g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0014g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0014g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0014g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0014g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0014g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0015g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0015g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0015g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0015g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0015g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0015g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0016g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0016g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0016g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0016g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0016g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0016g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0017g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0017g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0017g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0017g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0018g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0018g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0018g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0018g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0019g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0019g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0019g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0019g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0020g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0020g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0020g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0021g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0021g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0021g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0021g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0022g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0022g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0022g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0023g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0023g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0024g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0024g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0024g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0025g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0025g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0025g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0026g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0026g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0026g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0027g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0027g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0028g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0028g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0029g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0029g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0030g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0030g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0032g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0033g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0034g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0035g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0037g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0038g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0039g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0040g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0041g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0042g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0044g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0045g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0046g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0047g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0048g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0049g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0050g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0051g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0052g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0053g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0054g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0055g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0056g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0057g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0058g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0059g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0060g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0061g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0062g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0063g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0064g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0001t0065g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0002t0012g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0002t0017g0021 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0002t0023g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0003t0031g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0003t0036g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0003t0043g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0007t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0001c0008t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0002c0004t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| a0003c0005t0012g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0172 | EUR | GBR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0260 | EUR | GBR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0236 | EUR | GBR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0259 | EUR | GBR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00280 | hp1 | a0001 | c0001 | t0018 | g0253 | EUR | FIN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00280 | hp2 | a0001 | c0001 | t0010 | g0231 | EUR | FIN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0162 | EUR | FIN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0254 | EUR | FIN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00408 | hp2 | a0001 | c0001 | t0006 | g0245 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00621 | hp1 | a0001 | c0001 | t0014 | g0107 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0179 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00642 | hp1 | a0001 | c0001 | t0055 | g0032 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00673 | hp2 | a0001 | c0001 | t0016 | g0244 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0232 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00738 | hp1 | a0001 | c0001 | t0009 | g0128 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00738 | hp2 | a0001 | c0001 | t0008 | g0039 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00741 | hp1 | a0001 | c0001 | t0025 | g0126 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0211 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0157 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01069 | hp2 | a0001 | c0001 | t0009 | g0122 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01070 | hp1 | a0001 | c0001 | t0020 | g0010 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01070 | hp2 | a0001 | c0001 | t0017 | g0204 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01071 | hp1 | a0001 | c0001 | t0009 | g0123 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01071 | hp2 | a0001 | c0001 | t0020 | g0010 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0275 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01099 | hp2 | a0001 | c0001 | t0064 | g0121 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0040 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0229 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01109 | hp2 | a0001 | c0001 | t0012 | g0234 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0017 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01167 | hp2 | a0001 | c0001 | t0025 | g0127 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01168 | hp1 | a0001 | c0001 | t0009 | g0008 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01168 | hp2 | a0001 | c0001 | t0044 | g0106 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01169 | hp1 | a0001 | c0001 | t0009 | g0008 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0017 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01175 | hp1 | a0001 | c0001 | t0016 | g0210 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0276 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0194 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01243 | hp1 | a0001 | c0001 | t0057 | g0027 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0188 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01256 | hp2 | a0001 | c0001 | t0015 | g0012 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0208 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01257 | hp2 | a0001 | c0001 | t0007 | g0034 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01346 | hp1 | a0001 | c0001 | t0009 | g0120 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01358 | hp1 | a0001 | c0001 | t0007 | g0274 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01361 | hp1 | a0001 | c0001 | t0012 | g0013 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01361 | hp2 | a0001 | c0001 | t0009 | g0125 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0116 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01515 | hp1 | a0001 | c0001 | t0012 | g0139 | EUR | IBS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0009 | EUR | IBS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01516 | hp1 | a0003 | c0005 | t0012 | g0290 | EUR | IBS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0011 | EUR | IBS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | IBS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01517 | hp2 | a0001 | c0001 | t0008 | g0009 | EUR | IBS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01884 | hp1 | a0001 | c0001 | t0045 | g0233 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0112 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01891 | hp1 | a0001 | c0001 | t0062 | g0119 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01928 | hp1 | a0001 | c0001 | t0024 | g0149 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01943 | hp1 | a0001 | c0001 | t0052 | g0209 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01943 | hp2 | a0001 | c0001 | t0012 | g0196 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01978 | hp1 | a0001 | c0001 | t0009 | g0124 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01981 | hp1 | a0001 | c0001 | t0020 | g0201 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01981 | hp2 | a0001 | c0001 | t0015 | g0289 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0258 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0158 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02027 | hp1 | a0001 | c0001 | t0014 | g0272 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02040 | hp2 | a0001 | c0001 | t0010 | g0078 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0268 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02056 | hp2 | a0001 | c0001 | t0017 | g0246 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02074 | hp1 | a0001 | c0001 | t0016 | g0015 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02074 | hp2 | a0001 | c0001 | t0049 | g0262 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02080 | hp1 | a0001 | c0001 | t0011 | g0166 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02080 | hp2 | a0001 | c0001 | t0014 | g0288 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02083 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0222 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02129 | hp1 | a0001 | c0006 | t0001 | g0081 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02132 | hp1 | a0001 | c0001 | t0039 | g0152 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02132 | hp2 | a0001 | c0001 | t0026 | g0190 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02135 | hp1 | a0001 | c0001 | t0018 | g0099 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0098 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0013 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0160 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02148 | hp2 | a0001 | c0001 | t0017 | g0218 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02165 | hp1 | a0001 | c0001 | t0024 | g0257 | EAS | CDX | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0180 | EAS | CDX | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0129 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02258 | hp1 | a0001 | c0001 | t0061 | g0028 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02258 | hp2 | a0001 | c0001 | t0065 | g0312 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0308 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02273 | hp2 | a0001 | c0001 | t0038 | g0181 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02280 | hp1 | a0001 | c0001 | t0037 | g0041 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02293 | hp1 | a0001 | c0001 | t0020 | g0147 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0151 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02572 | hp1 | a0001 | c0003 | t0043 | g0024 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02615 | hp1 | a0001 | c0001 | t0022 | g0055 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02698 | hp1 | a0001 | c0001 | t0047 | g0020 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02717 | hp1 | a0001 | c0001 | t0060 | g0023 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0057 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02735 | hp2 | a0001 | c0007 | t0005 | g0183 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02738 | hp1 | a0001 | c0001 | t0028 | g0292 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0035 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02809 | hp1 | a0001 | c0001 | t0012 | g0022 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02809 | hp2 | a0001 | c0001 | t0027 | g0045 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02886 | hp1 | a0001 | c0001 | t0019 | g0278 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02886 | hp2 | a0001 | c0001 | t0023 | g0002 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0132 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0133 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02922 | hp1 | a0001 | c0002 | t0023 | g0169 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02976 | hp1 | a0001 | c0001 | t0033 | g0105 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02976 | hp2 | a0001 | c0001 | t0042 | g0101 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03041 | hp1 | a0001 | c0001 | t0048 | g0038 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03041 | hp2 | a0001 | c0001 | t0019 | g0134 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03098 | hp1 | a0001 | c0001 | t0041 | g0056 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0108 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03130 | hp2 | a0001 | c0001 | t0019 | g0243 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03139 | hp2 | a0001 | c0001 | t0059 | g0307 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03225 | hp1 | a0001 | c0002 | t0012 | g0029 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03225 | hp2 | a0001 | c0003 | t0031 | g0019 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0052 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03490 | hp1 | a0001 | c0001 | t0017 | g0006 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03490 | hp2 | a0001 | c0001 | t0025 | g0118 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03492 | hp1 | a0001 | c0001 | t0019 | g0006 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03492 | hp2 | a0001 | c0001 | t0028 | g0031 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03540 | hp1 | a0002 | c0004 | t0008 | g0171 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03540 | hp2 | a0001 | c0001 | t0022 | g0053 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03579 | hp2 | a0001 | c0001 | t0022 | g0054 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03654 | hp1 | a0001 | c0001 | t0046 | g0156 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03654 | hp2 | a0001 | c0001 | t0035 | g0205 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03669 | hp2 | a0001 | c0001 | t0063 | g0117 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03704 | hp1 | a0001 | c0001 | t0029 | g0042 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0167 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03831 | hp2 | a0001 | c0001 | t0011 | g0168 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03834 | hp2 | a0001 | c0001 | t0011 | g0036 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG03942 | hp2 | a0001 | c0001 | t0011 | g0193 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG04115 | hp1 | a0001 | c0001 | t0034 | g0220 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0213 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG04184 | hp2 | a0001 | c0001 | t0026 | g0164 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG04199 | hp1 | a0001 | c0001 | t0011 | g0073 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0185 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0255 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG04228 | hp1 | a0001 | c0001 | t0010 | g0084 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG04228 | hp2 | a0001 | c0001 | t0029 | g0311 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0030 | AFR | YRI | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0140 | AFR | YRI | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18747 | hp1 | a0001 | c0001 | t0006 | g0302 | EAS | CHB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18747 | hp2 | a0001 | c0001 | t0010 | g0241 | EAS | CHB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18906 | hp2 | a0001 | c0003 | t0036 | g0058 | AFR | YRI | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18939 | hp2 | a0001 | c0001 | t0016 | g0015 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18941 | hp1 | a0001 | c0001 | t0013 | g0264 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18941 | hp2 | a0001 | c0001 | t0021 | g0163 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18948 | hp1 | a0001 | c0001 | t0010 | g0087 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18951 | hp1 | a0001 | c0001 | t0006 | g0066 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18954 | hp1 | a0001 | c0001 | t0026 | g0165 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18954 | hp2 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18963 | hp1 | a0001 | c0001 | t0021 | g0144 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18963 | hp2 | a0001 | c0001 | t0018 | g0005 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18965 | hp1 | a0001 | c0001 | t0013 | g0142 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18965 | hp2 | a0001 | c0001 | t0014 | g0287 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0226 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18969 | hp1 | a0001 | c0001 | t0013 | g0131 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18969 | hp2 | a0001 | c0001 | t0032 | g0113 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18970 | hp1 | a0001 | c0001 | t0011 | g0305 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18971 | hp2 | a0001 | c0001 | t0021 | g0146 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18973 | hp2 | a0001 | c0001 | t0030 | g0069 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18979 | hp1 | a0001 | c0001 | t0015 | g0310 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18979 | hp2 | a0001 | c0001 | t0013 | g0282 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18981 | hp2 | a0001 | c0001 | t0013 | g0177 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18983 | hp1 | a0001 | c0008 | t0001 | g0286 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18983 | hp2 | a0001 | c0001 | t0014 | g0079 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18984 | hp2 | a0001 | c0001 | t0014 | g0273 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18987 | hp2 | a0001 | c0001 | t0056 | g0223 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18989 | hp2 | a0001 | c0001 | t0051 | g0187 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0067 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18993 | hp1 | a0001 | c0001 | t0013 | g0155 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18998 | hp2 | a0001 | c0001 | t0018 | g0005 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19003 | hp1 | a0001 | c0001 | t0053 | g0076 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19004 | hp2 | a0001 | c0001 | t0006 | g0159 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0300 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19007 | hp2 | a0001 | c0001 | t0014 | g0004 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19012 | hp1 | a0001 | c0001 | t0021 | g0263 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | LWK | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19030 | hp2 | a0001 | c0001 | t0050 | g0061 | AFR | LWK | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | LWK | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | LWK | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19060 | hp2 | a0001 | c0001 | t0030 | g0068 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19064 | hp1 | a0001 | c0001 | t0016 | g0227 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19072 | hp2 | a0001 | c0001 | t0018 | g0110 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19077 | hp2 | a0001 | c0001 | t0013 | g0291 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19078 | hp2 | a0001 | c0001 | t0024 | g0178 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19081 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19083 | hp1 | a0001 | c0001 | t0010 | g0256 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19085 | hp1 | a0001 | c0001 | t0016 | g0239 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19086 | hp1 | a0001 | c0001 | t0016 | g0075 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19087 | hp2 | a0001 | c0001 | t0013 | g0283 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19090 | hp1 | a0001 | c0001 | t0015 | g0309 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19090 | hp2 | a0001 | c0001 | t0054 | g0261 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | YRI | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA19240 | hp2 | a0001 | c0001 | t0058 | g0252 | AFR | YRI | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | ASW | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0090 | AFR | ASW | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | GIH | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | GIH | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02109 | hp1 | a0001 | c0001 | t0040 | g0136 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | USA | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| HG06807 | hp2 | a0001 | c0001 | t0027 | g0026 | AFR | USA | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18955 | hp1 | a0001 | c0001 | t0015 | g0175 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0299 | AFR | USA | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0161 | AFR | USA | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0037 | AFR | LWK | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| NA21309 | hp2 | a0001 | c0001 | t0011 | g0184 | AFR | LWK | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0023 | g0014 | REF | REF | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0017 | g0021 | REF | REF | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:114942347
|
T | A | 1 | a0002 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.167T>A | p.Met56Lys | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/5 | 817/5373 | 167/741 | 56/246 | chr7 | 114942347 | ||
| chr7:114979634
|
G | A | 1 | a0003 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.346G>A | p.Gly116Arg | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/5 | 996/5373 | 346/741 | 116/246 | chr7 | 114979634 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:114979543
|
C | A | 7 | a0001c0001a0001c0003a0001c0006others(4): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
synonymous_variant | LOW | c.255C>A | p.Ala85Ala | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/5 | 905/5373 | 255/741 | 85/246 | chr7 | 114979543 | ||
| chr7:114979642
|
A | G | 1 | a0001c0008 | 1 | NA18983.hp1 | synonymous_variant | LOW | c.354A>G | p.Ala118Ala | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/5 | 1004/5373 | 354/741 | 118/246 | chr7 | 114979642 | ||
| chr7:115015764
|
G | A | 1 | a0001c0003 | 3 | HG02572.hp1 HG03225.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.570G>A | p.Ala190Ala | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1220/5373 | 570/741 | 190/246 | chr7 | 115015764 | ||
| chr7:115015794
|
C | T | 1 | a0001c0007 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.600C>T | p.Cys200Cys | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1250/5373 | 600/741 | 200/246 | chr7 | 115015794 | ||
| chr7:115015812
|
C | T | 1 | a0001c0006 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.618C>T | p.Asp206Asp | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1268/5373 | 618/741 | 206/246 | chr7 | 115015812 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:114922169
|
G | A | 1 | a0001c0003t0031 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-575G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 865 | chr7 | 114922169 | |||||
| chr7:114922213
|
G | T | 1 | a0001c0001t0026 | 3 | HG02132.hp2 HG04184.hp2 NA18954.hp1 |
5_prime_UTR_variant | MODIFIER | c.-531G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 821 | chr7 | 114922213 | |||||
| chr7:114922219
|
G | A | 1 | a0001c0001t0032 | 1 | NA18969.hp2 | 5_prime_UTR_variant | MODIFIER | c.-525G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 815 | chr7 | 114922219 | |||||
| chr7:114922303
|
G | A | 1 | a0001c0001t0033 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-441G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 731 | chr7 | 114922303 | |||||
| chr7:114922368
|
C | T | 6 | a0001c0001t0009a0001c0001t0025a0001c0001t0062others(3): Show | 17 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-376C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 666 | chr7 | 114922368 | |||||
| chr7:114922376
|
G | A | 2 | a0001c0001t0034a0001c0001t0035 | 2 | HG03654.hp2 HG04115.hp1 |
5_prime_UTR_variant | MODIFIER | c.-368G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 658 | chr7 | 114922376 | |||||
| chr7:114922520
|
T | C | 1 | a0001c0003t0036 | 1 | NA18906.hp2 | 5_prime_UTR_variant | MODIFIER | c.-224T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 514 | chr7 | 114922520 | |||||
| chr7:114922982
|
C | CGGGCGGC others(5): Show |
1 | a0001c0001t0030 | 2 | NA18973.hp2 NA19060.hp2 |
5_prime_UTR_variant | MODIFIER | c.-51_-40dupGGGCGGCG others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/5 | 39 | INFO_REALIGN_3_PRIME | chr7 | 114922982 | ||||
| chr7:114922999
|
G | C | 1 | a0001c0001t0030 | 2 | NA18973.hp2 NA19060.hp2 |
5_prime_UTR_variant | MODIFIER | c.-35G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/5 | 35 | chr7 | 114922999 | |||||
| chr7:115016227
|
A | G | 4 | a0001c0001t0058a0001c0001t0059a0001c0001t0060others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*292A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 292 | chr7 | 115016227 | |||||
| chr7:115016240
|
T | C | 2 | a0001c0001t0022a0001c0001t0037 | 4 | HG02280.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*305T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 305 | chr7 | 115016240 | |||||
| chr7:115016323
|
C | G | 1 | a0001c0001t0057 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*388C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 388 | chr7 | 115016323 | |||||
| chr7:115016495
|
T | C | 1 | a0001c0001t0038 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*560T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 560 | chr7 | 115016495 | |||||
| chr7:115016498
|
C | T | 1 | a0001c0001t0056 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*563C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 563 | chr7 | 115016498 | |||||
| chr7:115016558
|
G | A | 1 | a0001c0001t0039 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*623G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 623 | chr7 | 115016558 | |||||
| chr7:115016644
|
C | CTAAA | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*753dupTAAA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 754 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | ||||
| chr7:115016644
|
C | CTAAATAA others(1): Show |
6 | a0001c0001t0006a0001c0001t0018a0001c0001t0021others(3): Show | 28 | HG00280.hp1 HG00408.hp2 HG00621.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*746_*753dupTAAATA others(2): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 754 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | ||||
| chr7:115016644
|
C | CTAAATAA others(5): Show |
4 | a0001c0001t0024a0001c0001t0052a0001c0001t0053others(1): Show | 6 | HG01928.hp1 HG01943.hp1 HG02165.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*742_*753dupTAAATA others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 754 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | ||||
| chr7:115016644
|
C | CTAAATAA others(9): Show |
1 | a0001c0001t0055 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*738_*753dupTAAATA others(10): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 754 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | ||||
| chr7:115016644
|
CTAAA | C | 1 | a0001c0001t0014 | 7 | HG00621.hp1 HG02027.hp1 HG02080.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*753delTAAA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 750 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | ||||
| chr7:115016644
|
CTAAATAA others(1): Show |
C | 3 | a0001c0001t0019a0001c0001t0022a0001c0001t0063 | 8 | HG02615.hp1 HG02886.hp1 HG03041.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*746_*753delTAAATA others(2): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 746 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | ||||
| chr7:115016644
|
CTAAATAA others(17): Show |
C | 2 | a0001c0001t0040a0001c0001t0062 | 2 | HG01891.hp1 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*730_*753delTAAATA others(18): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 730 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | ||||
| chr7:115016685
|
T | C | 7 | a0001c0001t0022a0001c0001t0037a0001c0001t0041others(4): Show | 9 | HG02280.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*750T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 750 | chr7 | 115016685 | |||||
| chr7:115016685
|
T | TAAAC | 3 | a0001c0001t0061a0001c0003t0031a0001c0003t0043 | 3 | HG02258.hp1 HG02572.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*755_*758dupAAAC | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 759 | INFO_REALIGN_3_PRIME | chr7 | 115016685 | ||||
| chr7:115016685
|
T | TAAATAAA others(5): Show |
1 | a0001c0001t0051 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*753_*754insTAAATA others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 754 | INFO_REALIGN_3_PRIME | chr7 | 115016685 | ||||
| chr7:115016835
|
G | A | 1 | a0001c0001t0022 | 3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*900G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 900 | chr7 | 115016835 | |||||
| chr7:115016914
|
C | T | 1 | a0001c0001t0042 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*979C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 979 | chr7 | 115016914 | |||||
| chr7:115016942
|
A | G | 1 | a0001c0001t0042 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1007A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1007 | chr7 | 115016942 | |||||
| chr7:115016990
|
A | G | 1 | a0001c0001t0033 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1055A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1055 | chr7 | 115016990 | |||||
| chr7:115017522
|
T | C | 1 | a0001c0001t0047 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1587T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1587 | chr7 | 115017522 | |||||
| chr7:115017533
|
C | A | 2 | a0001c0001t0022a0001c0001t0037 | 4 | HG02280.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1598C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1598 | chr7 | 115017533 | |||||
| chr7:115017621
|
A | C | 1 | a0001c0001t0060 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1686 | chr7 | 115017621 | |||||
| chr7:115017842
|
A | G | 1 | a0001c0001t0020 | 4 | HG01070.hp1 HG01071.hp2 HG01981.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1907A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1907 | chr7 | 115017842 | |||||
| chr7:115017967
|
A | G | 1 | a0001c0001t0046 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2032A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2032 | chr7 | 115017967 | |||||
| chr7:115018140
|
G | T | 2 | a0001c0001t0028a0001c0001t0029 | 4 | HG02738.hp1 HG03492.hp2 HG03704.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2205G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2205 | chr7 | 115018140 | |||||
| chr7:115018166
|
A | G | 45 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(42): Show | 193 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*2231A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2231 | chr7 | 115018166 | |||||
| chr7:115018194
|
A | C | 2 | a0001c0001t0042a0001c0001t0050 | 2 | HG02976.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2259A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2259 | chr7 | 115018194 | |||||
| chr7:115018244
|
A | T | 1 | a0001c0001t0045 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2309A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2309 | chr7 | 115018244 | |||||
| chr7:115018278
|
A | C | 1 | a0001c0001t0022 | 3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2343A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2343 | chr7 | 115018278 | |||||
| chr7:115018432
|
A | G | 18 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(15): Show | 89 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*2497A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2497 | chr7 | 115018432 | |||||
| chr7:115018585
|
T | C | 1 | a0001c0001t0044 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2650T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2650 | chr7 | 115018585 | |||||
| chr7:115018751
|
C | A | 2 | a0001c0001t0022a0001c0001t0037 | 4 | HG02280.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2816C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2816 | chr7 | 115018751 | |||||
| chr7:115018892
|
A | C | 1 | a0001c0001t0037 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2957A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2957 | chr7 | 115018892 | |||||
| chr7:115018909
|
C | T | 2 | a0001c0001t0022a0001c0001t0037 | 4 | HG02280.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2974C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2974 | chr7 | 115018909 | |||||
| chr7:115018951
|
G | T | 2 | a0001c0001t0022a0001c0001t0037 | 4 | HG02280.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3016G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3016 | chr7 | 115018951 | |||||
| chr7:115019009
|
G | GT | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(6): Show | 53 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3086dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3087 | INFO_REALIGN_3_PRIME | chr7 | 115019009 | ||||
| chr7:115019009
|
GT | G | 8 | a0001c0001t0005a0001c0001t0015a0001c0001t0021others(5): Show | 37 | HG00408.hp1 HG00735.hp2 HG01192.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3086delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3086 | INFO_REALIGN_3_PRIME | chr7 | 115019009 | ||||
| chr7:115019089
|
G | A | 2 | a0001c0001t0048a0001c0001t0065 | 2 | HG02258.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3154G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3154 | chr7 | 115019089 | |||||
| chr7:115019180
|
G | A | 2 | a0001c0001t0013a0001c0001t0049 | 9 | HG02074.hp2 NA18941.hp1 NA18965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3245G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3245 | chr7 | 115019180 | |||||
| chr7:115019260
|
T | C | 8 | a0001c0001t0001a0001c0001t0010a0001c0001t0014others(5): Show | 74 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*3325T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3325 | chr7 | 115019260 | |||||
| chr7:115019294
|
G | C | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(6): Show | 53 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3359G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3359 | chr7 | 115019294 | |||||
| chr7:115019441
|
A | T | 9 | a0001c0001t0003a0001c0001t0012a0001c0001t0018others(6): Show | 39 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3506A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3506 | chr7 | 115019441 | |||||
| chr7:115019483
|
A | T | 9 | a0001c0001t0042a0001c0001t0050a0001c0001t0058others(6): Show | 9 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3548A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3548 | chr7 | 115019483 | |||||
| chr7:115019722
|
A | G | 3 | a0001c0001t0059a0001c0001t0060a0001c0001t0061 | 3 | HG02258.hp1 HG02717.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3787A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3787 | chr7 | 115019722 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:114922762
|
G | A | 1 | a0001c0001t0008g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-108+126G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/4 | chr7 | 114922762 | ||||||
| chr7:114922778
|
G | GTT | 224 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0114others(221): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-108+143_-108+144i others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 114922778 | |||||
| chr7:114923146
|
G | T | 6 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(3): Show | 6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+19G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114923146 | ||||||
| chr7:114923225
|
G | T | 1 | a0001c0001t0065g0312 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.94+98G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114923225 | ||||||
| chr7:114923232
|
T | C | 1 | a0001c0001t0014g0107 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.94+105T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114923232 | ||||||
| chr7:114923300
|
T | C | 2 | a0001c0001t0009g0108a0001c0001t0065g0312 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.94+173T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114923300 | ||||||
| chr7:114924227
|
A | G | 1 | a0001c0001t0029g0311 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.94+1100A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114924227 | ||||||
| chr7:114924249
|
C | A | 1 | a0001c0001t0005g0109 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.94+1122C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114924249 | ||||||
| chr7:114924508
|
A | C | 3 | a0001c0001t0005g0308a0001c0001t0015g0309a0001c0001t0015g0310 | 3 | HG02273.hp1 NA18979.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.94+1381A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114924508 | ||||||
| chr7:114924525
|
G | A | 1 | a0001c0001t0018g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.94+1398G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114924525 | ||||||
| chr7:114924587
|
T | TAGC | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(292): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.94+1461_94+1462ins others(3): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114924587 | |||||
| chr7:114924623
|
A | G | 1 | a0001c0001t0059g0307 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.94+1496A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114924623 | ||||||
| chr7:114925288
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(292): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.94+2161A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114925288 | ||||||
| chr7:114925409
|
T | C | 1 | a0001c0001t0004g0111 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.94+2282T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114925409 | ||||||
| chr7:114925643
|
G | A | 1 | a0001c0001t0009g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.94+2516G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114925643 | ||||||
| chr7:114926068
|
T | C | 1 | a0001c0003t0031g0019 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94+2941T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926068 | ||||||
| chr7:114926214
|
A | T | 275 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.94+3087A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926214 | ||||||
| chr7:114926510
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0293a0001c0001t0001g0294others(12): Show | 18 | HG00408.hp1 HG02523.hp2 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+3383C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926510 | ||||||
| chr7:114926535
|
G | A | 1 | a0001c0001t0047g0020 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.94+3408G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926535 | ||||||
| chr7:114926834
|
A | G | 1 | a0001c0001t0028g0292 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.94+3707A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926834 | ||||||
| chr7:114926894
|
G | T | 1 | a0001c0001t0013g0291 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.94+3767G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926894 | ||||||
| chr7:114926937
|
C | A | 1 | a0001c0001t0009g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.94+3810C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926937 | ||||||
| chr7:114927325
|
C | CT | 306 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(303): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.94+4212dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114927325 | |||||
| chr7:114927325
|
C | CTT | 11 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(8): Show | 11 | HG01168.hp2 HG01516.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+4211_94+4212dup others(2): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114927325 | |||||
| chr7:114927455
|
C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(228): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.94+4328C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114927455 | ||||||
| chr7:114927517
|
A | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0247a0001c0001t0001g0250others(54): Show | 60 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.94+4390A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114927517 | ||||||
| chr7:114927741
|
C | T | 6 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(3): Show | 6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+4614C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114927741 | ||||||
| chr7:114927800
|
C | A | 1 | a0001c0001t0010g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94+4673C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114927800 | ||||||
| chr7:114927984
|
GC | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(228): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.94+4858delC | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114927984 | ||||||
| chr7:114928049
|
A | G | 49 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0219others(46): Show | 50 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.94+4922A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114928049 | ||||||
| chr7:114928125
|
A | T | 1 | a0001c0001t0044g0106 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.94+4998A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114928125 | ||||||
| chr7:114928324
|
C | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(267): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.94+5197C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114928324 | ||||||
| chr7:114928557
|
T | C | 38 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(35): Show | 39 | HG00609.hp1 HG02015.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.94+5430T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114928557 | ||||||
| chr7:114928677
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.94+5550A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114928677 | ||||||
| chr7:114929037
|
A | G | 6 | a0001c0001t0010g0057a0001c0001t0022g0053a0001c0001t0022g0054others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+5910A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929037 | ||||||
| chr7:114929055
|
A | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0091others(155): Show | 167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.94+5928A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929055 | ||||||
| chr7:114929084
|
G | GATCTATC others(9): Show |
2 | a0001c0001t0005g0129a0001c0001t0022g0053 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.94+5961_94+5976dup others(16): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929084 | |||||
| chr7:114929084
|
G | GATCTATC others(13): Show |
23 | a0001c0001t0001g0130a0001c0001t0002g0044a0001c0001t0002g0203others(20): Show | 23 | HG01070.hp2 HG01168.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.94+5976_94+5977ins others(20): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929084 | |||||
| chr7:114929084
|
G | GATCTATC others(17): Show |
131 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0092others(128): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.94+5976_94+5977ins others(24): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929084 | |||||
| chr7:114929084
|
G | GATCTATC others(21): Show |
83 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0097others(80): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.94+5976_94+5977ins others(28): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929084 | |||||
| chr7:114929084
|
G | GATCTATC others(25): Show |
15 | a0001c0001t0001g0192a0001c0001t0001g0304a0001c0001t0001g0306others(12): Show | 15 | HG00621.hp1 HG00738.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.94+5976_94+5977ins others(32): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929084 | |||||
| chr7:114929084
|
G | GATCTATC others(17): Show |
1 | a0001c0001t0005g0194 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.94+5971_94+5972ins others(24): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929084 | |||||
| chr7:114929088
|
T | TATCTATC others(10): Show |
39 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(36): Show | 40 | HG00609.hp1 HG02015.hp2 HG02040.hp2 others(37): Show |
intron_variant | MODIFIER | c.94+5976_94+5977ins others(17): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929088 | |||||
| chr7:114929273
|
A | G | 1 | a0001c0003t0036g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.94+6146A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929273 | ||||||
| chr7:114929307
|
C | A | 14 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(11): Show | 15 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.94+6180C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929307 | ||||||
| chr7:114929327
|
C | T | 1 | a0001c0001t0062g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.94+6200C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929327 | ||||||
| chr7:114929481
|
G | A | 6 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(3): Show | 6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+6354G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929481 | ||||||
| chr7:114929547
|
A | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(228): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.94+6420A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929547 | ||||||
| chr7:114929715
|
A | C | 1 | a0001c0001t0037g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.94+6588A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929715 | ||||||
| chr7:114929722
|
A | G | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+6595A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929722 | ||||||
| chr7:114929754
|
A | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(228): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.94+6627A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929754 | ||||||
| chr7:114929783
|
G | A | 1 | a0001c0001t0020g0010 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.94+6656G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929783 | ||||||
| chr7:114929845
|
G | A | 4 | a0001c0001t0012g0022a0001c0001t0037g0041a0001c0001t0060g0023others(1): Show | 4 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+6718G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929845 | ||||||
| chr7:114930602
|
T | G | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+7475T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114930602 | ||||||
| chr7:114930797
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0295a0001c0001t0001g0301others(3): Show | 9 | NA18939.hp1 NA18942.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+7670T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114930797 | ||||||
| chr7:114931083
|
CTCTT | C | 6 | a0001c0001t0010g0057a0001c0001t0022g0053a0001c0001t0022g0054others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+7958_94+7961del others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114931083 | |||||
| chr7:114931096
|
C | T | 1 | a0001c0003t0036g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.94+7969C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931096 | ||||||
| chr7:114931214
|
A | G | 1 | a0001c0001t0013g0264 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.94+8087A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931214 | ||||||
| chr7:114931290
|
G | A | 6 | a0001c0001t0001g0135a0001c0001t0011g0132a0001c0001t0011g0133others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+8163G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931290 | ||||||
| chr7:114931308
|
C | T | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+8181C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931308 | ||||||
| chr7:114931493
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.94+8366G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931493 | ||||||
| chr7:114931795
|
G | A | 1 | a0001c0001t0005g0240 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.94+8668G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931795 | ||||||
| chr7:114931796
|
T | C | 3 | a0001c0001t0003g0170a0001c0001t0005g0137a0001c0001t0005g0138 | 3 | NA18970.hp2 NA19058.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.94+8669T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931796 | ||||||
| chr7:114931974
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | NA18982.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.94+8847G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931974 | ||||||
| chr7:114932000
|
C | T | 5 | a0001c0001t0010g0057a0001c0001t0022g0053a0001c0001t0022g0054others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+8873C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932000 | ||||||
| chr7:114932125
|
G | A | 6 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(3): Show | 6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+8998G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932125 | ||||||
| chr7:114932135
|
A | G | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+9008A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932135 | ||||||
| chr7:114932191
|
G | C | 5 | a0001c0001t0010g0057a0001c0001t0022g0053a0001c0001t0022g0054others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+9064G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932191 | ||||||
| chr7:114932526
|
G | A | 1 | a0001c0001t0012g0139 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.94+9399G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932526 | ||||||
| chr7:114932546
|
G | A | 1 | a0001c0001t0006g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.94+9419G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932546 | ||||||
| chr7:114932616
|
C | T | 1 | a0001c0001t0025g0118 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.94+9489C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932616 | ||||||
| chr7:114932670
|
G | T | 1 | a0001c0002t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.94+9543G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932670 | ||||||
| chr7:114932677
|
G | T | 1 | a0001c0001t0011g0168 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.94+9550G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932677 | ||||||
| chr7:114932685
|
G | A | 1 | a0001c0001t0032g0113 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.94+9558G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932685 | ||||||
| chr7:114932739
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.95-9536G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932739 | ||||||
| chr7:114932835
|
A | G | 6 | a0001c0001t0010g0057a0001c0001t0022g0053a0001c0001t0022g0054others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-9440A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932835 | ||||||
| chr7:114933089
|
G | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(267): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.95-9186G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933089 | ||||||
| chr7:114933253
|
C | CA | 3 | a0001c0001t0008g0018a0001c0001t0008g0140a0002c0004t0008g0171 | 3 | HG03453.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.95-9022_95-9021ins others(1): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933253 | ||||||
| chr7:114933253
|
C | CT | 240 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(237): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.95-9005dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114933253 | |||||
| chr7:114933314
|
A | G | 2 | a0001c0001t0003g0191a0001c0001t0011g0168 | 2 | HG01433.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.95-8961A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933314 | ||||||
| chr7:114933345
|
G | T | 49 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0219others(46): Show | 50 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.95-8930G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933345 | ||||||
| chr7:114933362
|
G | A | 1 | a0001c0001t0008g0009 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.95-8913G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933362 | ||||||
| chr7:114933373
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(273): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.95-8902T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933373 | ||||||
| chr7:114933564
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.95-8711C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933564 | ||||||
| chr7:114933777
|
A | C | 1 | a0001c0001t0002g0050 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.95-8498A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933777 | ||||||
| chr7:114933824
|
T | C | 2 | a0001c0001t0002g0224a0001c0001t0004g0208 | 2 | HG01256.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.95-8451T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933824 | ||||||
| chr7:114933916
|
C | T | 1 | a0001c0001t0015g0310 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.95-8359C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933916 | ||||||
| chr7:114933917
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.95-8358G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933917 | ||||||
| chr7:114933932
|
T | A | 1 | a0001c0001t0004g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.95-8343T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933932 | ||||||
| chr7:114934024
|
C | T | 2 | a0001c0001t0008g0039a0001c0001t0008g0040 | 2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.95-8251C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114934024 | ||||||
| chr7:114934025
|
G | A | 1 | a0001c0001t0027g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.95-8250G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114934025 | ||||||
| chr7:114934184
|
A | G | 3 | a0001c0001t0013g0264a0001c0001t0013g0283a0001c0001t0021g0263 | 3 | NA18941.hp1 NA19012.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.95-8091A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114934184 | ||||||
| chr7:114934552
|
A | T | 6 | a0001c0001t0013g0264a0001c0001t0013g0282a0001c0001t0013g0283others(3): Show | 6 | HG02074.hp2 NA18941.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-7723A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114934552 | ||||||
| chr7:114934692
|
C | T | 16 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(13): Show | 17 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-7583C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114934692 | ||||||
| chr7:114935026
|
A | G | 1 | a0001c0001t0002g0060 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.95-7249A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935026 | ||||||
| chr7:114935037
|
G | T | 1 | a0001c0001t0002g0260 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.95-7238G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935037 | ||||||
| chr7:114935250
|
T | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(293): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.95-7025T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935250 | ||||||
| chr7:114935390
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.95-6885T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935390 | ||||||
| chr7:114935468
|
T | A | 1 | a0001c0001t0009g0120 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.95-6807T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935468 | ||||||
| chr7:114935532
|
G | GT | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(227): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.95-6734dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114935532 | |||||
| chr7:114935800
|
T | C | 1 | a0001c0001t0052g0209 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.95-6475T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935800 | ||||||
| chr7:114935814
|
G | T | 1 | a0001c0001t0012g0139 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.95-6461G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935814 | ||||||
| chr7:114935917
|
A | G | 1 | a0001c0001t0013g0131 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.95-6358A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935917 | ||||||
| chr7:114936015
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.95-6260T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114936015 | ||||||
| chr7:114936060
|
G | T | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.95-6215G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114936060 | ||||||
| chr7:114936541
|
A | G | 5 | a0001c0001t0010g0057a0001c0001t0022g0053a0001c0001t0022g0054others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-5734A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114936541 | ||||||
| chr7:114936597
|
A | G | 3 | a0001c0001t0013g0264a0001c0001t0013g0283a0001c0001t0021g0263 | 3 | NA18941.hp1 NA19012.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.95-5678A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114936597 | ||||||
| chr7:114936737
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.95-5538G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114936737 | ||||||
| chr7:114936878
|
CATTG | C | 6 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(3): Show | 6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-5393_95-5390del others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114936878 | |||||
| chr7:114936973
|
T | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(228): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.95-5302T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114936973 | ||||||
| chr7:114937054
|
A | C | 1 | a0001c0001t0048g0038 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.95-5221A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937054 | ||||||
| chr7:114937084
|
A | G | 1 | a0001c0001t0002g0281 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.95-5191A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937084 | ||||||
| chr7:114937212
|
G | A | 1 | a0001c0002t0002g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.95-5063G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937212 | ||||||
| chr7:114937330
|
T | C | 1 | a0001c0001t0012g0013 | 2 | HG01361.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.95-4945T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937330 | ||||||
| chr7:114937458
|
T | C | 14 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(11): Show | 15 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-4817T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937458 | ||||||
| chr7:114937460
|
T | A | 8 | a0001c0001t0001g0247a0001c0001t0004g0016a0001c0001t0004g0284others(5): Show | 9 | HG00408.hp2 HG00673.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-4815T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937460 | ||||||
| chr7:114937527
|
G | C | 7 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0071others(4): Show | 7 | NA18940.hp2 NA18951.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-4748G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937527 | ||||||
| chr7:114937678
|
G | A | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.95-4597G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937678 | ||||||
| chr7:114937779
|
G | A | 1 | a0001c0002t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.95-4496G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937779 | ||||||
| chr7:114937798
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0002g0088 | 2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.95-4477C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937798 | ||||||
| chr7:114938474
|
C | A | 1 | a0001c0001t0029g0042 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.95-3801C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114938474 | ||||||
| chr7:114938741
|
G | T | 1 | a0001c0001t0003g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.95-3534G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114938741 | ||||||
| chr7:114938799
|
AC | A | 316 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(313): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.95-3473delC | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114938799 | |||||
| chr7:114938858
|
C | G | 6 | a0001c0001t0010g0057a0001c0001t0022g0053a0001c0001t0022g0054others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-3417C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114938858 | ||||||
| chr7:114938903
|
C | T | 1 | a0001c0001t0011g0166 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.95-3372C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114938903 | ||||||
| chr7:114938908
|
T | C | 6 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(3): Show | 6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-3367T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114938908 | ||||||
| chr7:114939097
|
C | CATATG | 11 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(8): Show | 12 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-3178_95-3177ins others(5): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939097 | ||||||
| chr7:114939098
|
C | G | 11 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(8): Show | 12 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-3177C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939098 | ||||||
| chr7:114939099
|
A | G | 11 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(8): Show | 12 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-3176A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939099 | ||||||
| chr7:114939101
|
C | A | 11 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(8): Show | 12 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-3174C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939101 | ||||||
| chr7:114939102
|
A | G | 11 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(8): Show | 12 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-3173A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939102 | ||||||
| chr7:114939157
|
A | G | 3 | a0001c0001t0026g0164a0001c0001t0026g0165a0001c0001t0026g0190 | 3 | HG02132.hp2 HG04184.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.95-3118A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939157 | ||||||
| chr7:114939377
|
T | C | 5 | a0001c0001t0002g0014a0001c0001t0002g0225a0001c0001t0007g0211others(2): Show | 5 | HG00642.hp2 HG00741.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-2898T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939377 | ||||||
| chr7:114939588
|
GC | G | 4 | a0001c0001t0012g0022a0001c0001t0037g0041a0001c0001t0060g0023others(1): Show | 4 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2685delC | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114939588 | |||||
| chr7:114939685
|
C | G | 2 | a0001c0001t0001g0189a0001c0001t0006g0300 | 2 | NA18982.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.95-2590C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939685 | ||||||
| chr7:114939699
|
A | G | 1 | a0001c0001t0004g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.95-2576A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939699 | ||||||
| chr7:114939788
|
C | T | 1 | a0001c0001t0015g0309 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.95-2487C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939788 | ||||||
| chr7:114939924
|
A | T | 1 | a0001c0001t0010g0087 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.95-2351A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939924 | ||||||
| chr7:114939929
|
G | C | 1 | a0001c0001t0010g0087 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.95-2346G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939929 | ||||||
| chr7:114939931
|
A | C | 1 | a0001c0001t0010g0087 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.95-2344A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939931 | ||||||
| chr7:114939980
|
T | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(237): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.95-2295T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939980 | ||||||
| chr7:114940002
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0014g0004 | 3 | HG00673.hp1 HG02040.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.95-2273A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940002 | ||||||
| chr7:114940016
|
T | G | 38 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(35): Show | 39 | HG00609.hp1 HG02015.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.95-2259T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940016 | ||||||
| chr7:114940036
|
A | C | 38 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(35): Show | 39 | HG00609.hp1 HG02015.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.95-2239A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940036 | ||||||
| chr7:114940198
|
T | C | 6 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(3): Show | 6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-2077T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940198 | ||||||
| chr7:114940265
|
T | C | 1 | a0001c0001t0027g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.95-2010T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940265 | ||||||
| chr7:114940342
|
T | G | 6 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(3): Show | 6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-1933T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940342 | ||||||
| chr7:114940458
|
G | A | 5 | a0001c0001t0010g0057a0001c0001t0022g0053a0001c0001t0022g0054others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-1817G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940458 | ||||||
| chr7:114940510
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.95-1765G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940510 | ||||||
| chr7:114940553
|
A | T | 1 | a0001c0003t0036g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.95-1722A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940553 | ||||||
| chr7:114940977
|
GTC | G | 38 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(35): Show | 39 | HG00609.hp1 HG02015.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.95-1292_95-1291del others(2): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114940977 | |||||
| chr7:114941167
|
C | T | 2 | a0001c0001t0022g0053a0001c0001t0022g0054 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.95-1108C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114941167 | ||||||
| chr7:114941346
|
G | A | 1 | a0001c0001t0013g0142 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.95-929G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114941346 | ||||||
| chr7:114941453
|
C | T | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.95-822C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114941453 | ||||||
| chr7:114941674
|
A | T | 1 | a0001c0001t0040g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.95-601A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114941674 | ||||||
| chr7:114941795
|
C | T | 1 | a0001c0002t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.95-480C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114941795 | ||||||
| chr7:114941870
|
C | T | 1 | a0001c0001t0051g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.95-405C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114941870 | ||||||
| chr7:114942034
|
G | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(275): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.95-241G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114942034 | ||||||
| chr7:114942107
|
A | G | 3 | a0001c0001t0003g0170a0001c0001t0005g0137a0001c0001t0005g0138 | 3 | NA18970.hp2 NA19058.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.95-168A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114942107 | ||||||
| chr7:114942136
|
G | A | 16 | a0001c0001t0009g0008a0001c0001t0009g0108a0001c0001t0009g0112others(13): Show | 17 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-139G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114942136 | ||||||
| chr7:114942469
|
C | T | 6 | a0001c0001t0010g0057a0001c0001t0022g0053a0001c0001t0022g0054others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+72C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114942469 | ||||||
| chr7:114942640
|
C | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(293): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.217+243C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114942640 | ||||||
| chr7:114942966
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(230): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.217+569C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114942966 | ||||||
| chr7:114942983
|
C | T | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+586C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114942983 | ||||||
| chr7:114942984
|
G | A | 16 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0092others(13): Show | 18 | HG00099.hp1 HG01099.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.217+587G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114942984 | ||||||
| chr7:114943033
|
C | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(9): Show | 13 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.217+636C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943033 | ||||||
| chr7:114943043
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(230): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.217+646T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943043 | ||||||
| chr7:114943402
|
A | G | 1 | a0001c0001t0021g0163 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.217+1005A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943402 | ||||||
| chr7:114943432
|
A | T | 1 | a0001c0001t0011g0193 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.217+1035A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943432 | ||||||
| chr7:114943517
|
G | A | 1 | a0001c0001t0004g0296 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.217+1120G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943517 | ||||||
| chr7:114943521
|
T | C | 1 | a0001c0001t0059g0307 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.217+1124T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943521 | ||||||
| chr7:114943622
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | NA18982.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.217+1225A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943622 | ||||||
| chr7:114943702
|
A | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(230): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.217+1305A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943702 | ||||||
| chr7:114943936
|
C | CA | 4 | a0001c0001t0010g0030a0001c0001t0057g0027a0001c0001t0061g0028others(1): Show | 4 | HG01243.hp1 HG02258.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+1545dupA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114943936 | |||||
| chr7:114944023
|
A | G | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+1626A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944023 | ||||||
| chr7:114944256
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.217+1859G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944256 | ||||||
| chr7:114944312
|
G | A | 1 | a0001c0001t0004g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.217+1915G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944312 | ||||||
| chr7:114944398
|
T | A | 1 | a0001c0001t0008g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.217+2001T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944398 | ||||||
| chr7:114944448
|
A | T | 4 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0019g0243others(1): Show | 4 | HG02886.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+2051A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944448 | ||||||
| chr7:114944477
|
T | A | 1 | a0001c0003t0036g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.217+2080T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944477 | ||||||
| chr7:114944677
|
G | A | 16 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0092others(13): Show | 18 | HG00099.hp1 HG01099.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.217+2280G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944677 | ||||||
| chr7:114944743
|
G | C | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+2346G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944743 | ||||||
| chr7:114944992
|
T | C | 57 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0145others(54): Show | 59 | HG00621.hp2 HG01069.hp1 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.217+2595T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944992 | ||||||
| chr7:114945295
|
G | T | 2 | a0001c0001t0004g0249a0001c0001t0004g0277 | 2 | HG02523.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.217+2898G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114945295 | ||||||
| chr7:114945614
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(230): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.217+3217A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114945614 | ||||||
| chr7:114945681
|
G | C | 6 | a0001c0001t0010g0057a0001c0001t0022g0053a0001c0001t0022g0054others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+3284G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114945681 | ||||||
| chr7:114945750
|
C | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(293): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.217+3353C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114945750 | ||||||
| chr7:114945763
|
T | C | 1 | a0001c0001t0016g0244 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.217+3366T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114945763 | ||||||
| chr7:114946002
|
C | T | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+3605C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114946002 | ||||||
| chr7:114946225
|
A | AGT | 18 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(15): Show | 19 | HG01433.hp2 HG02055.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.217+3859_217+3860d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114946225 | |||||
| chr7:114946225
|
A | AGTGT | 8 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(5): Show | 8 | HG01168.hp2 HG02257.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.217+3857_217+3860d others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114946225 | |||||
| chr7:114946225
|
AGT | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.217+3859_217+3860d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114946225 | |||||
| chr7:114946225
|
AGTGT | A | 53 | a0001c0001t0001g0086a0001c0001t0001g0206a0001c0001t0001g0207others(50): Show | 54 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.217+3857_217+3860d others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114946225 | |||||
| chr7:114946225
|
AGTGTGT | A | 14 | a0001c0001t0001g0094a0001c0001t0002g0281a0001c0001t0009g0008others(11): Show | 15 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.217+3855_217+3860d others(8): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114946225 | |||||
| chr7:114946265
|
C | T | 1 | a0001c0001t0003g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.217+3868C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114946265 | ||||||
| chr7:114946468
|
A | G | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+4071A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114946468 | ||||||
| chr7:114946727
|
G | A | 1 | a0001c0001t0006g0300 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.217+4330G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114946727 | ||||||
| chr7:114946820
|
G | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(230): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.217+4423G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114946820 | ||||||
| chr7:114946848
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(230): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.217+4451C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114946848 | ||||||
| chr7:114947239
|
C | T | 7 | a0001c0001t0002g0260a0001c0001t0004g0258a0001c0001t0007g0017others(4): Show | 8 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.217+4842C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947239 | ||||||
| chr7:114947305
|
C | T | 1 | a0001c0001t0005g0158 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.217+4908C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947305 | ||||||
| chr7:114947370
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(230): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.217+4973A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947370 | ||||||
| chr7:114947377
|
A | G | 3 | a0001c0001t0002g0260a0001c0001t0004g0258a0001c0001t0007g0259 | 3 | HG00099.hp2 HG00140.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.217+4980A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947377 | ||||||
| chr7:114947534
|
T | C | 1 | a0001c0007t0005g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.217+5137T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947534 | ||||||
| chr7:114947667
|
G | C | 4 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(1): Show | 4 | HG02257.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+5270G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947667 | ||||||
| chr7:114947710
|
G | A | 34 | a0001c0001t0001g0091a0001c0001t0001g0141a0001c0001t0001g0145others(31): Show | 35 | HG01192.hp2 HG01928.hp1 HG01981.hp2 others(32): Show |
intron_variant | MODIFIER | c.217+5313G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947710 | ||||||
| chr7:114947786
|
G | A | 1 | a0001c0001t0021g0144 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.217+5389G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947786 | ||||||
| chr7:114947938
|
G | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.217+5541G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947938 | ||||||
| chr7:114948205
|
A | G | 1 | a0001c0001t0062g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.217+5808A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948205 | ||||||
| chr7:114948222
|
C | CT | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(292): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.217+5827dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114948222 | |||||
| chr7:114948254
|
G | A | 2 | a0001c0001t0002g0251a0001c0001t0002g0266 | 2 | HG01192.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.217+5857G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948254 | ||||||
| chr7:114948478
|
C | T | 1 | a0001c0001t0035g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.217+6081C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948478 | ||||||
| chr7:114948485
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(231): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.217+6088A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948485 | ||||||
| chr7:114948505
|
C | T | 1 | a0001c0002t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.217+6108C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948505 | ||||||
| chr7:114948649
|
A | G | 2 | a0001c0001t0002g0186a0001c0001t0004g0185 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.217+6252A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948649 | ||||||
| chr7:114948820
|
C | A | 1 | a0001c0001t0025g0127 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.217+6423C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948820 | ||||||
| chr7:114948925
|
A | G | 1 | a0001c0001t0024g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.217+6528A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948925 | ||||||
| chr7:114948964
|
T | C | 4 | a0001c0001t0006g0212a0001c0001t0006g0226a0001c0001t0016g0227others(1): Show | 4 | NA18954.hp2 NA18966.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+6567T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948964 | ||||||
| chr7:114949100
|
C | A | 1 | a0001c0001t0002g0281 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.217+6703C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114949100 | ||||||
| chr7:114949106
|
T | C | 1 | a0001c0001t0006g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.217+6709T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114949106 | ||||||
| chr7:114949440
|
G | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.217+7043G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114949440 | ||||||
| chr7:114949704
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.217+7307T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114949704 | ||||||
| chr7:114949790
|
TA | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(293): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.217+7396delA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114949790 | |||||
| chr7:114949806
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.217+7409G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114949806 | ||||||
| chr7:114949966
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.217+7569G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114949966 | ||||||
| chr7:114950173
|
G | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(236): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.217+7776G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950173 | ||||||
| chr7:114950253
|
G | A | 2 | a0001c0001t0009g0108a0001c0001t0065g0312 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.217+7856G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950253 | ||||||
| chr7:114950282
|
T | C | 1 | a0001c0001t0007g0229 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.217+7885T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950282 | ||||||
| chr7:114950391
|
G | A | 1 | a0001c0001t0007g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.217+7994G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950391 | ||||||
| chr7:114950747
|
A | T | 2 | a0001c0001t0022g0053a0001c0001t0022g0054 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.217+8350A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950747 | ||||||
| chr7:114950832
|
G | A | 1 | a0001c0001t0006g0226 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.217+8435G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950832 | ||||||
| chr7:114950874
|
A | G | 1 | a0001c0003t0036g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.217+8477A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950874 | ||||||
| chr7:114950976
|
A | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(281): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.217+8579A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950976 | ||||||
| chr7:114951248
|
CT | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(238): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.217+8852delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951248 | ||||||
| chr7:114951345
|
GA | G | 58 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0145others(55): Show | 61 | HG00621.hp2 HG01069.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.217+8958delA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114951345 | |||||
| chr7:114951407
|
C | T | 11 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(8): Show | 12 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.217+9010C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951407 | ||||||
| chr7:114951411
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.217+9014A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951411 | ||||||
| chr7:114951448
|
A | G | 7 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(4): Show | 7 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+9051A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951448 | ||||||
| chr7:114951449
|
A | G | 1 | a0001c0001t0004g0208 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.217+9052A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951449 | ||||||
| chr7:114951610
|
C | T | 1 | a0001c0001t0017g0204 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.217+9213C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951610 | ||||||
| chr7:114951660
|
G | GT | 19 | a0001c0001t0001g0063a0001c0001t0002g0002a0001c0001t0002g0043others(16): Show | 20 | HG01106.hp1 HG01361.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.217+9272dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114951660 | |||||
| chr7:114951710
|
T | G | 1 | a0001c0002t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.217+9313T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951710 | ||||||
| chr7:114951869
|
C | A | 1 | a0001c0001t0013g0282 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.217+9472C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951869 | ||||||
| chr7:114951970
|
C | G | 5 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0019g0243others(2): Show | 5 | HG02572.hp1 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+9573C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951970 | ||||||
| chr7:114951979
|
G | C | 1 | a0001c0001t0057g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.217+9582G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951979 | ||||||
| chr7:114951994
|
G | A | 74 | a0001c0001t0001g0086a0001c0001t0001g0219a0001c0001t0002g0014others(71): Show | 76 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.217+9597G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951994 | ||||||
| chr7:114952121
|
T | C | 1 | a0001c0001t0009g0125 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.217+9724T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952121 | ||||||
| chr7:114952178
|
A | G | 43 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0001g0195others(40): Show | 44 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.217+9781A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952178 | ||||||
| chr7:114952212
|
T | C | 44 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0219others(41): Show | 46 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.217+9815T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952212 | ||||||
| chr7:114952328
|
C | A | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.217+9931C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952328 | ||||||
| chr7:114952349
|
G | A | 3 | a0001c0001t0003g0191a0001c0001t0005g0232a0001c0001t0012g0234 | 3 | HG00735.hp2 HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.217+9952G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952349 | ||||||
| chr7:114952382
|
C | G | 1 | a0001c0001t0021g0163 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.217+9985C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952382 | ||||||
| chr7:114952416
|
A | AT | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(108): Show | 118 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.217+10031dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114952416 | |||||
| chr7:114952461
|
A | G | 6 | a0001c0001t0005g0095a0001c0001t0005g0096a0001c0001t0005g0151others(3): Show | 6 | HG00408.hp2 HG01981.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.217+10064A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952461 | ||||||
| chr7:114952710
|
G | GA | 6 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG01099.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.217+10320dupA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114952710 | |||||
| chr7:114952823
|
G | A | 1 | a0001c0001t0002g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.217+10426G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952823 | ||||||
| chr7:114952824
|
A | T | 5 | a0001c0001t0002g0049a0001c0001t0002g0102a0001c0001t0002g0103others(2): Show | 5 | HG02257.hp2 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+10427A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952824 | ||||||
| chr7:114952921
|
C | T | 1 | a0001c0001t0010g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.217+10524C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952921 | ||||||
| chr7:114952931
|
A | G | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+10534A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952931 | ||||||
| chr7:114952933
|
G | A | 73 | a0001c0001t0001g0195a0001c0001t0001g0206a0001c0001t0001g0207others(70): Show | 76 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.217+10536G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952933 | ||||||
| chr7:114953166
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0022g0053a0001c0001t0022g0054others(1): Show | 5 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+10769T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114953166 | ||||||
| chr7:114953279
|
T | C | 7 | a0001c0001t0002g0046a0001c0001t0002g0049a0001c0001t0002g0102others(4): Show | 7 | HG01433.hp2 HG02257.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+10882T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114953279 | ||||||
| chr7:114953604
|
T | A | 2 | a0001c0001t0059g0307a0001c0003t0031g0019 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.217+11207T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114953604 | ||||||
| chr7:114953677
|
G | A | 2 | a0001c0001t0002g0203a0001c0001t0008g0299 | 2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.217+11280G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114953677 | ||||||
| chr7:114953810
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(121): Show | 132 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.217+11413A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114953810 | ||||||
| chr7:114953834
|
A | G | 2 | a0001c0001t0012g0022a0001c0001t0033g0105 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.217+11437A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114953834 | ||||||
| chr7:114954116
|
C | T | 2 | a0001c0001t0012g0022a0001c0001t0033g0105 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.217+11719C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954116 | ||||||
| chr7:114954135
|
C | A | 1 | a0001c0001t0004g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.217+11738C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954135 | ||||||
| chr7:114954257
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0022g0053a0001c0001t0022g0054others(1): Show | 5 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+11860G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954257 | ||||||
| chr7:114954277
|
T | G | 8 | a0001c0001t0001g0115a0001c0001t0002g0203a0001c0001t0007g0268others(5): Show | 8 | HG01496.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.217+11880T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954277 | ||||||
| chr7:114954582
|
T | G | 1 | a0001c0001t0004g0277 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.217+12185T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954582 | ||||||
| chr7:114954750
|
C | A | 1 | a0001c0001t0011g0193 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.217+12353C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954750 | ||||||
| chr7:114954897
|
C | T | 1 | a0001c0001t0007g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.217+12500C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954897 | ||||||
| chr7:114954975
|
G | C | 2 | a0001c0001t0005g0161a0001c0001t0005g0303 | 2 | HG00408.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.217+12578G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954975 | ||||||
| chr7:114955190
|
A | G | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | NA18944.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.217+12793A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955190 | ||||||
| chr7:114955234
|
T | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(116): Show | 126 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.217+12837T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955234 | ||||||
| chr7:114955392
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | NA18944.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.217+12995G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955392 | ||||||
| chr7:114955392
|
G | T | 3 | a0001c0001t0007g0211a0001c0001t0007g0229a0001c0001t0007g0259 | 3 | HG00140.hp2 HG00741.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.217+12995G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955392 | ||||||
| chr7:114955440
|
G | A | 1 | a0001c0001t0018g0099 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.217+13043G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955440 | ||||||
| chr7:114955488
|
A | G | 1 | a0001c0001t0009g0128 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.217+13091A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955488 | ||||||
| chr7:114955779
|
C | T | 1 | a0001c0001t0065g0312 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.217+13382C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955779 | ||||||
| chr7:114955799
|
A | G | 306 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(303): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.217+13402A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955799 | ||||||
| chr7:114955873
|
C | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(308): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.217+13476C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955873 | ||||||
| chr7:114955975
|
T | A | 2 | a0001c0001t0019g0243a0001c0001t0019g0278 | 2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.217+13578T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955975 | ||||||
| chr7:114956162
|
G | C | 1 | a0001c0001t0021g0146 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.217+13765G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956162 | ||||||
| chr7:114956219
|
A | C | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+13822A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956219 | ||||||
| chr7:114956322
|
C | G | 3 | a0001c0001t0004g0016a0001c0001t0004g0284a0001c0001t0006g0016 | 3 | HG02071.hp2 HG02129.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.217+13925C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956322 | ||||||
| chr7:114956348
|
TAC | T | 4 | a0001c0001t0007g0034a0001c0001t0007g0035a0001c0001t0007g0157others(1): Show | 4 | HG01069.hp1 HG01257.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+13961_217+1396 others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114956348 | |||||
| chr7:114956358
|
C | CAT | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 121 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.217+13973_217+1397 others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114956358 | |||||
| chr7:114956358
|
C | CATAT | 6 | a0001c0001t0001g0247a0001c0001t0014g0107a0001c0001t0014g0273others(3): Show | 6 | HG00621.hp1 HG02080.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+13971_217+1397 others(8): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114956358 | |||||
| chr7:114956358
|
C | T | 4 | a0001c0001t0007g0034a0001c0001t0007g0035a0001c0001t0007g0157others(1): Show | 4 | HG01069.hp1 HG01257.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+13961C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956358 | ||||||
| chr7:114956425
|
A | C | 8 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0048others(5): Show | 9 | HG01361.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.217+14028A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956425 | ||||||
| chr7:114956786
|
T | G | 25 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(22): Show | 26 | HG01168.hp2 HG01361.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.217+14389T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956786 | ||||||
| chr7:114956951
|
G | T | 311 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(308): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.217+14554G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956951 | ||||||
| chr7:114957230
|
T | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(121): Show | 132 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.217+14833T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114957230 | ||||||
| chr7:114957258
|
G | T | 315 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(312): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.217+14861G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114957258 | ||||||
| chr7:114957402
|
G | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(308): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.217+15005G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114957402 | ||||||
| chr7:114957453
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(116): Show | 126 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.217+15056A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114957453 | ||||||
| chr7:114958157
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0022g0053a0001c0001t0022g0054others(1): Show | 5 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+15760C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958157 | ||||||
| chr7:114958202
|
C | T | 25 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(22): Show | 26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.217+15805C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958202 | ||||||
| chr7:114958208
|
T | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(312): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.217+15811T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958208 | ||||||
| chr7:114958310
|
C | A | 4 | a0001c0001t0003g0191a0001c0001t0005g0232a0001c0001t0012g0234others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+15913C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958310 | ||||||
| chr7:114958437
|
G | A | 2 | a0001c0001t0005g0137a0001c0001t0005g0138 | 2 | NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.217+16040G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958437 | ||||||
| chr7:114958716
|
A | T | 1 | a0001c0001t0003g0217 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.217+16319A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958716 | ||||||
| chr7:114958852
|
C | T | 1 | a0001c0001t0003g0077 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.217+16455C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958852 | ||||||
| chr7:114959506
|
A | G | 26 | a0001c0001t0001g0195a0001c0001t0005g0003a0001c0001t0005g0012others(23): Show | 27 | HG00408.hp2 HG01192.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.217+17109A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114959506 | ||||||
| chr7:114959513
|
C | T | 1 | a0001c0001t0004g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.217+17116C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114959513 | ||||||
| chr7:114959601
|
A | G | 1 | a0001c0001t0010g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.217+17204A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114959601 | ||||||
| chr7:114959824
|
C | CTAA | 100 | a0001c0001t0001g0007a0001c0001t0001g0189a0001c0001t0001g0195others(97): Show | 105 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.217+17456_217+1745 others(7): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114959824 | |||||
| chr7:114959824
|
C | CTAATAA | 156 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(153): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.217+17453_217+1745 others(10): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114959824 | |||||
| chr7:114959824
|
C | CTAATAAT others(2): Show |
52 | a0001c0001t0001g0080a0001c0001t0001g0115a0001c0001t0001g0192others(49): Show | 54 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.217+17450_217+1745 others(13): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114959824 | |||||
| chr7:114959824
|
C | CTAATAAT others(5): Show |
1 | a0001c0001t0010g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.217+17447_217+1745 others(16): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114959824 | |||||
| chr7:114959824
|
CTAA | C | 4 | a0001c0001t0010g0057a0001c0001t0058g0252a0001c0001t0060g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+17456_217+1745 others(7): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114959824 | |||||
| chr7:114959913
|
C | T | 1 | a0001c0002t0012g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.217+17516C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114959913 | ||||||
| chr7:114960292
|
G | A | 1 | a0001c0001t0011g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.217+17895G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960292 | ||||||
| chr7:114960395
|
C | T | 5 | a0001c0001t0005g0012a0001c0001t0005g0160a0001c0001t0005g0308others(2): Show | 5 | HG01256.hp2 HG01358.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+17998C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960395 | ||||||
| chr7:114960484
|
A | T | 25 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(22): Show | 26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.217+18087A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960484 | ||||||
| chr7:114960494
|
G | A | 1 | a0001c0001t0010g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.217+18097G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960494 | ||||||
| chr7:114960517
|
T | G | 1 | a0001c0001t0027g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.217+18120T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960517 | ||||||
| chr7:114960625
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0022g0053a0001c0001t0022g0054others(1): Show | 5 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+18228G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960625 | ||||||
| chr7:114960628
|
T | C | 1 | a0001c0001t0003g0213 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.217+18231T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960628 | ||||||
| chr7:114961039
|
G | A | 12 | a0001c0001t0002g0186a0001c0001t0007g0034a0001c0001t0007g0035others(9): Show | 13 | HG00738.hp2 HG01069.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.218-18467G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114961039 | ||||||
| chr7:114961280
|
T | A | 4 | a0001c0001t0010g0057a0001c0001t0058g0252a0001c0001t0060g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-18226T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114961280 | ||||||
| chr7:114961413
|
G | A | 4 | a0001c0001t0010g0057a0001c0001t0058g0252a0001c0001t0060g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-18093G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114961413 | ||||||
| chr7:114961421
|
G | A | 1 | a0001c0001t0005g0303 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.218-18085G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114961421 | ||||||
| chr7:114961472
|
G | GTGCTCAA others(38): Show |
1 | a0001c0001t0034g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.218-18031_218-1798 others(49): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114961472 | |||||
| chr7:114961825
|
C | T | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218-17681C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114961825 | ||||||
| chr7:114962043
|
C | T | 1 | a0001c0001t0016g0239 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.218-17463C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962043 | ||||||
| chr7:114962318
|
T | C | 4 | a0001c0001t0016g0015a0001c0001t0016g0244a0001c0001t0017g0246others(1): Show | 5 | HG00673.hp2 HG02056.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.218-17188T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962318 | ||||||
| chr7:114962446
|
C | A | 5 | a0001c0001t0001g0007a0001c0001t0022g0053a0001c0001t0022g0054others(2): Show | 6 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-17060C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962446 | ||||||
| chr7:114962513
|
A | G | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218-16993A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962513 | ||||||
| chr7:114962789
|
A | G | 1 | a0001c0001t0010g0084 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.218-16717A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962789 | ||||||
| chr7:114962817
|
A | C | 1 | a0001c0001t0001g0294 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.218-16689A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962817 | ||||||
| chr7:114962909
|
A | T | 2 | a0001c0001t0012g0022a0001c0001t0033g0105 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.218-16597A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962909 | ||||||
| chr7:114963003
|
G | A | 1 | a0001c0001t0037g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.218-16503G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963003 | ||||||
| chr7:114963025
|
G | T | 2 | a0001c0001t0059g0307a0001c0003t0031g0019 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.218-16481G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963025 | ||||||
| chr7:114963355
|
C | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 131 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.218-16151C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963355 | ||||||
| chr7:114963372
|
T | A | 4 | a0001c0001t0002g0088a0001c0001t0002g0143a0001c0001t0002g0230others(1): Show | 4 | HG01496.hp1 HG02698.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-16134T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963372 | ||||||
| chr7:114963498
|
A | T | 1 | a0001c0001t0004g0296 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.218-16008A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963498 | ||||||
| chr7:114963728
|
G | A | 2 | a0001c0001t0022g0053a0001c0001t0022g0054 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.218-15778G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963728 | ||||||
| chr7:114963868
|
C | G | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-15638C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963868 | ||||||
| chr7:114963931
|
T | G | 1 | a0001c0001t0014g0272 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.218-15575T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963931 | ||||||
| chr7:114964043
|
T | C | 1 | a0001c0001t0004g0208 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.218-15463T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964043 | ||||||
| chr7:114964227
|
A | G | 310 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(307): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.218-15279A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964227 | ||||||
| chr7:114964492
|
TC | T | 150 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0206others(147): Show | 156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.218-15010delC | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114964492 | |||||
| chr7:114964493
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(124): Show | 135 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.218-15013C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964493 | ||||||
| chr7:114964494
|
C | T | 150 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0206others(147): Show | 156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.218-15012C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964494 | ||||||
| chr7:114964525
|
ACTTCCCT others(8): Show |
A | 2 | a0001c0001t0037g0041a0001c0001t0050g0061 | 2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218-14966_218-1495 others(19): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114964525 | |||||
| chr7:114964622
|
C | A | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218-14884C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964622 | ||||||
| chr7:114964637
|
G | A | 150 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0206others(147): Show | 156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.218-14869G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964637 | ||||||
| chr7:114964652
|
G | A | 1 | a0001c0001t0005g0151 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.218-14854G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964652 | ||||||
| chr7:114964693
|
G | A | 2 | a0001c0001t0060g0023a0001c0001t0061g0028 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.218-14813G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964693 | ||||||
| chr7:114964709
|
C | T | 2 | a0001c0001t0003g0200a0001c0001t0003g0216 | 2 | HG01928.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.218-14797C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964709 | ||||||
| chr7:114964827
|
G | C | 1 | a0001c0001t0006g0245 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.218-14679G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964827 | ||||||
| chr7:114964828
|
C | A | 1 | a0001c0001t0006g0245 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.218-14678C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964828 | ||||||
| chr7:114964843
|
C | T | 1 | a0001c0001t0024g0257 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.218-14663C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964843 | ||||||
| chr7:114965141
|
C | T | 310 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(307): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.218-14365C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114965141 | ||||||
| chr7:114965444
|
G | A | 1 | a0001c0001t0005g0161 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.218-14062G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114965444 | ||||||
| chr7:114966054
|
A | G | 1 | a0001c0001t0005g0129 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218-13452A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114966054 | ||||||
| chr7:114966405
|
C | CA | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(121): Show | 131 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.218-13085dupA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114966405 | |||||
| chr7:114966405
|
CAAAAAAA | C | 25 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(22): Show | 26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-13091_218-1308 others(11): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114966405 | |||||
| chr7:114966510
|
A | T | 1 | a0001c0001t0006g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.218-12996A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114966510 | ||||||
| chr7:114966524
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(103): Show | 112 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.218-12982C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114966524 | ||||||
| chr7:114966979
|
T | A | 6 | a0001c0001t0010g0030a0001c0001t0012g0022a0001c0001t0012g0139others(3): Show | 6 | HG01515.hp1 HG02132.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-12527T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114966979 | ||||||
| chr7:114967026
|
T | A | 2 | a0001c0001t0059g0307a0001c0003t0031g0019 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.218-12480T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967026 | ||||||
| chr7:114967097
|
A | G | 2 | a0001c0001t0012g0022a0001c0001t0033g0105 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.218-12409A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967097 | ||||||
| chr7:114967138
|
T | G | 4 | a0001c0001t0002g0044a0001c0001t0002g0047a0001c0001t0002g0059others(1): Show | 4 | HG02622.hp1 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-12368T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967138 | ||||||
| chr7:114967139
|
T | C | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218-12367T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967139 | ||||||
| chr7:114967158
|
T | G | 3 | a0001c0001t0020g0010a0001c0001t0020g0147a0001c0001t0020g0201 | 4 | HG01070.hp1 HG01071.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-12348T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967158 | ||||||
| chr7:114967161
|
A | G | 25 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(22): Show | 26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-12345A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967161 | ||||||
| chr7:114967173
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.218-12333G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967173 | ||||||
| chr7:114967474
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(305): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.218-12032A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967474 | ||||||
| chr7:114967489
|
A | C | 1 | a0001c0001t0001g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.218-12017A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967489 | ||||||
| chr7:114967546
|
C | T | 4 | a0001c0001t0005g0109a0001c0001t0015g0309a0001c0001t0015g0310others(1): Show | 4 | HG02273.hp2 NA18979.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-11960C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967546 | ||||||
| chr7:114967568
|
A | T | 1 | a0001c0001t0012g0013 | 2 | HG01361.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.218-11938A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967568 | ||||||
| chr7:114967597
|
G | C | 1 | a0001c0001t0009g0120 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.218-11909G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967597 | ||||||
| chr7:114967608
|
G | A | 2 | a0001c0001t0030g0068a0001c0001t0030g0069 | 2 | NA18973.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.218-11898G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967608 | ||||||
| chr7:114967634
|
G | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0247a0001c0001t0001g0250others(9): Show | 13 | HG00621.hp1 HG00673.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.218-11872G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967634 | ||||||
| chr7:114967745
|
G | C | 3 | a0001c0001t0020g0010a0001c0001t0020g0147a0001c0001t0020g0201 | 4 | HG01070.hp1 HG01071.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-11761G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967745 | ||||||
| chr7:114967830
|
CT | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(252): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.218-11659delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114967830 | |||||
| chr7:114967830
|
CTT | C | 48 | a0001c0001t0001g0145a0001c0001t0001g0182a0001c0001t0001g0192others(45): Show | 49 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.218-11660_218-1165 others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114967830 | |||||
| chr7:114968136
|
A | T | 1 | a0001c0001t0006g0179 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.218-11370A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968136 | ||||||
| chr7:114968234
|
G | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0150 | 2 | NA18972.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.218-11272G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968234 | ||||||
| chr7:114968336
|
A | C | 1 | a0001c0001t0007g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.218-11170A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968336 | ||||||
| chr7:114968382
|
T | C | 9 | a0001c0001t0001g0007a0001c0001t0022g0053a0001c0001t0022g0054others(6): Show | 10 | HG02280.hp1 HG02615.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.218-11124T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968382 | ||||||
| chr7:114968567
|
G | A | 1 | a0001c0001t0010g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.218-10939G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968567 | ||||||
| chr7:114968814
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0019g0134 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.218-10692A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968814 | ||||||
| chr7:114968906
|
C | T | 2 | a0001c0001t0012g0022a0001c0001t0033g0105 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.218-10600C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968906 | ||||||
| chr7:114968975
|
G | A | 144 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0206others(141): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.218-10531G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968975 | ||||||
| chr7:114969043
|
C | T | 4 | a0001c0001t0010g0030a0001c0001t0012g0022a0001c0001t0033g0105others(1): Show | 4 | HG02809.hp1 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-10463C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969043 | ||||||
| chr7:114969205
|
C | T | 1 | a0001c0001t0051g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218-10301C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969205 | ||||||
| chr7:114969429
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.218-10077G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969429 | ||||||
| chr7:114969439
|
C | T | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218-10067C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969439 | ||||||
| chr7:114969465
|
G | A | 1 | a0001c0001t0003g0077 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.218-10041G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969465 | ||||||
| chr7:114969720
|
AT | A | 7 | a0001c0001t0001g0007a0001c0001t0022g0053a0001c0001t0022g0054others(4): Show | 8 | HG02280.hp1 HG02615.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.218-9785delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969720 | ||||||
| chr7:114969773
|
C | A | 1 | a0001c0001t0009g0120 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.218-9733C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969773 | ||||||
| chr7:114970163
|
G | A | 2 | a0001c0001t0002g0186a0001c0001t0047g0020 | 2 | HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.218-9343G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114970163 | ||||||
| chr7:114970197
|
G | A | 1 | a0001c0001t0025g0118 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.218-9309G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114970197 | ||||||
| chr7:114970445
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.218-9061C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114970445 | ||||||
| chr7:114970609
|
C | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(294): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.218-8897C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114970609 | ||||||
| chr7:114970786
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.218-8720T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114970786 | ||||||
| chr7:114970918
|
G | T | 3 | a0001c0001t0003g0202a0001c0001t0003g0279a0001c0001t0003g0280 | 3 | HG01891.hp2 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.218-8588G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114970918 | ||||||
| chr7:114971248
|
A | T | 1 | a0001c0001t0049g0262 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.218-8258A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971248 | ||||||
| chr7:114971313
|
C | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(309): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.218-8193C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971313 | ||||||
| chr7:114971362
|
G | T | 2 | a0001c0001t0040g0136a0001c0001t0062g0119 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.218-8144G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971362 | ||||||
| chr7:114971447
|
C | T | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-8059C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971447 | ||||||
| chr7:114971468
|
G | A | 1 | a0001c0006t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.218-8038G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971468 | ||||||
| chr7:114971479
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(309): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.218-8027A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971479 | ||||||
| chr7:114971515
|
T | C | 1 | a0001c0001t0006g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.218-7991T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971515 | ||||||
| chr7:114971624
|
G | A | 1 | a0001c0001t0010g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.218-7882G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971624 | ||||||
| chr7:114971731
|
G | C | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.218-7775G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971731 | ||||||
| chr7:114971857
|
G | T | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218-7649G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971857 | ||||||
| chr7:114971872
|
G | A | 1 | a0001c0001t0014g0273 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.218-7634G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971872 | ||||||
| chr7:114972054
|
C | T | 143 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0206others(140): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.218-7452C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972054 | ||||||
| chr7:114972288
|
A | T | 12 | a0001c0001t0002g0186a0001c0001t0007g0034a0001c0001t0007g0035others(9): Show | 13 | HG00738.hp2 HG01069.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.218-7218A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972288 | ||||||
| chr7:114972318
|
A | C | 2 | a0001c0001t0001g0091a0001c0001t0002g0228 | 2 | HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.218-7188A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972318 | ||||||
| chr7:114972406
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0022g0053a0001c0001t0022g0054others(1): Show | 5 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-7100C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972406 | ||||||
| chr7:114972549
|
A | G | 2 | a0001c0001t0060g0023a0001c0001t0061g0028 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.218-6957A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972549 | ||||||
| chr7:114972753
|
C | T | 25 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(22): Show | 26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-6753C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972753 | ||||||
| chr7:114972754
|
G | A | 1 | a0001c0001t0004g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.218-6752G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972754 | ||||||
| chr7:114972901
|
C | T | 1 | a0001c0001t0004g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.218-6605C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972901 | ||||||
| chr7:114972928
|
C | T | 2 | a0001c0001t0041g0056a0001c0003t0043g0024 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.218-6578C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972928 | ||||||
| chr7:114972953
|
C | G | 1 | a0001c0001t0003g0236 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.218-6553C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972953 | ||||||
| chr7:114973090
|
C | CAT | 16 | a0001c0001t0002g0060a0001c0001t0002g0102a0001c0001t0002g0103others(13): Show | 16 | HG01516.hp1 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.218-6416_218-6415i others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973090 | ||||||
| chr7:114973090
|
C | CATGT | 155 | a0001c0001t0001g0182a0001c0001t0001g0189a0001c0001t0001g0192others(152): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.218-6416_218-6415i others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973090 | ||||||
| chr7:114973090
|
C | CATGTGT | 3 | a0001c0001t0002g0230a0001c0001t0010g0090a0001c0001t0011g0184 | 3 | HG01496.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.218-6416_218-6415i others(8): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973090 | ||||||
| chr7:114973091
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(129): Show | 141 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.218-6415G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973091 | ||||||
| chr7:114973101
|
G | A | 158 | a0001c0001t0001g0182a0001c0001t0001g0189a0001c0001t0001g0192others(155): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.218-6405G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973101 | ||||||
| chr7:114973101
|
G | GTA | 4 | a0001c0001t0010g0030a0001c0001t0012g0022a0001c0001t0033g0105others(1): Show | 4 | HG02809.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-6385_218-6384d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114973101 | |||||
| chr7:114973101
|
G | GTGTATA | 5 | a0001c0001t0006g0302a0001c0001t0007g0211a0001c0001t0007g0275others(2): Show | 6 | HG00741.hp2 HG01081.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-6404_218-6403i others(8): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114973101 | |||||
| chr7:114973101
|
G | GTGTATAT others(3): Show |
1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.218-6404_218-6403i others(12): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114973101 | |||||
| chr7:114973101
|
G | GTGTGTAT others(3): Show |
2 | a0001c0001t0001g0007a0001c0001t0022g0055 | 3 | HG02615.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.218-6404_218-6403i others(12): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114973101 | |||||
| chr7:114973101
|
G | GTGTGTGT others(3): Show |
2 | a0001c0001t0022g0053a0001c0001t0022g0054 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.218-6404_218-6403i others(12): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114973101 | |||||
| chr7:114973103
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(115): Show | 125 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.218-6403A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973103 | ||||||
| chr7:114973143
|
G | A | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-6363G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973143 | ||||||
| chr7:114973220
|
A | G | 74 | a0001c0001t0001g0195a0001c0001t0001g0206a0001c0001t0001g0207others(71): Show | 77 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.218-6286A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973220 | ||||||
| chr7:114973281
|
C | G | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-6225C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973281 | ||||||
| chr7:114973464
|
G | T | 1 | a0001c0001t0002g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.218-6042G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973464 | ||||||
| chr7:114973783
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(60): Show | 67 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.218-5723T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973783 | ||||||
| chr7:114974176
|
T | A | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218-5330T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974176 | ||||||
| chr7:114974182
|
T | A | 1 | a0001c0001t0004g0208 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.218-5324T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974182 | ||||||
| chr7:114974208
|
T | C | 2 | a0001c0001t0037g0041a0001c0001t0050g0061 | 2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218-5298T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974208 | ||||||
| chr7:114974229
|
T | C | 1 | a0001c0001t0005g0129 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218-5277T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974229 | ||||||
| chr7:114974269
|
T | C | 1 | a0001c0001t0002g0281 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.218-5237T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974269 | ||||||
| chr7:114974297
|
TTA | T | 313 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(310): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.218-5195_218-5194d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114974297 | |||||
| chr7:114974359
|
G | A | 25 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(22): Show | 26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-5147G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974359 | ||||||
| chr7:114974437
|
C | G | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-5069C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974437 | ||||||
| chr7:114974584
|
T | A | 312 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(309): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.218-4922T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974584 | ||||||
| chr7:114974686
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0002g0228 | 2 | HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.218-4820T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974686 | ||||||
| chr7:114974744
|
A | G | 1 | a0001c0001t0007g0157 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.218-4762A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974744 | ||||||
| chr7:114974762
|
A | G | 1 | a0001c0001t0005g0160 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.218-4744A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974762 | ||||||
| chr7:114974919
|
T | C | 1 | a0001c0001t0002g0281 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.218-4587T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974919 | ||||||
| chr7:114975105
|
G | A | 1 | a0001c0001t0004g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.218-4401G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975105 | ||||||
| chr7:114975113
|
T | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(309): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.218-4393T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975113 | ||||||
| chr7:114975247
|
G | A | 1 | a0001c0001t0005g0137 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.218-4259G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975247 | ||||||
| chr7:114975261
|
G | T | 314 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(311): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.218-4245G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975261 | ||||||
| chr7:114975544
|
G | A | 2 | a0001c0001t0040g0136a0001c0001t0062g0119 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.218-3962G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975544 | ||||||
| chr7:114975561
|
CT | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(292): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.218-3932delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114975561 | |||||
| chr7:114975706
|
A | G | 1 | a0001c0001t0050g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.218-3800A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975706 | ||||||
| chr7:114975890
|
A | G | 1 | a0001c0001t0007g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.218-3616A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975890 | ||||||
| chr7:114975899
|
G | A | 4 | a0001c0001t0002g0049a0001c0001t0002g0102a0001c0001t0002g0103others(1): Show | 4 | HG02257.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-3607G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975899 | ||||||
| chr7:114976152
|
C | T | 1 | a0001c0002t0023g0169 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.218-3354C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976152 | ||||||
| chr7:114976247
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.218-3259G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976247 | ||||||
| chr7:114976420
|
C | T | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-3086C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976420 | ||||||
| chr7:114976545
|
T | A | 1 | a0001c0001t0015g0175 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.218-2961T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976545 | ||||||
| chr7:114976627
|
G | C | 9 | a0001c0001t0001g0007a0001c0001t0022g0053a0001c0001t0022g0054others(6): Show | 10 | HG02280.hp1 HG02615.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.218-2879G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976627 | ||||||
| chr7:114976633
|
A | G | 1 | a0001c0003t0031g0019 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.218-2873A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976633 | ||||||
| chr7:114976856
|
CT | C | 25 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(22): Show | 26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-2640delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114976856 | |||||
| chr7:114976862
|
T | C | 1 | a0001c0001t0018g0253 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.218-2644T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976862 | ||||||
| chr7:114977119
|
A | T | 25 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(22): Show | 26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-2387A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114977119 | ||||||
| chr7:114977495
|
C | T | 1 | a0001c0001t0010g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.218-2011C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114977495 | ||||||
| chr7:114977547
|
C | T | 1 | a0001c0001t0064g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.218-1959C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114977547 | ||||||
| chr7:114977591
|
C | G | 1 | a0001c0001t0037g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.218-1915C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114977591 | ||||||
| chr7:114977792
|
T | C | 1 | a0001c0001t0002g0281 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.218-1714T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114977792 | ||||||
| chr7:114977875
|
A | T | 9 | a0001c0001t0001g0007a0001c0001t0022g0053a0001c0001t0022g0054others(6): Show | 10 | HG02280.hp1 HG02615.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.218-1631A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114977875 | ||||||
| chr7:114978004
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.218-1502A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978004 | ||||||
| chr7:114978111
|
C | T | 2 | a0001c0001t0040g0136a0001c0001t0062g0119 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.218-1395C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978111 | ||||||
| chr7:114978140
|
G | A | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-1366G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978140 | ||||||
| chr7:114978141
|
C | T | 25 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(22): Show | 26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-1365C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978141 | ||||||
| chr7:114978155
|
A | G | 1 | a0001c0001t0021g0144 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.218-1351A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978155 | ||||||
| chr7:114978393
|
C | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(9): Show | 13 | HG01361.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.218-1113C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978393 | ||||||
| chr7:114978428
|
G | T | 1 | a0001c0001t0013g0291 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.218-1078G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978428 | ||||||
| chr7:114978450
|
A | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(120): Show | 130 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.218-1056A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978450 | ||||||
| chr7:114978577
|
C | T | 312 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(309): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.218-929C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978577 | ||||||
| chr7:114978635
|
T | C | 2 | a0001c0001t0019g0243a0001c0001t0019g0278 | 2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.218-871T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978635 | ||||||
| chr7:114978649
|
AC | A | 5 | a0001c0001t0013g0131a0001c0001t0013g0142a0001c0001t0013g0155others(2): Show | 5 | NA18965.hp1 NA18969.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-856delC | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978649 | ||||||
| chr7:114978655
|
A | G | 2 | a0001c0001t0008g0037a0001c0001t0044g0106 | 2 | HG01168.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.218-851A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978655 | ||||||
| chr7:114978730
|
A | G | 4 | a0001c0001t0010g0030a0001c0001t0012g0022a0001c0001t0033g0105others(1): Show | 4 | HG02809.hp1 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-776A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978730 | ||||||
| chr7:114978857
|
A | T | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-649A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978857 | ||||||
| chr7:114978894
|
T | C | 2 | a0001c0001t0059g0307a0001c0003t0031g0019 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.218-612T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978894 | ||||||
| chr7:114979039
|
A | G | 25 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(22): Show | 26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-467A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114979039 | ||||||
| chr7:114979152
|
A | G | 2 | a0001c0001t0041g0056a0001c0003t0043g0024 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.218-354A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114979152 | ||||||
| chr7:114979277
|
A | G | 1 | a0001c0001t0003g0238 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.218-229A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114979277 | ||||||
| chr7:114979460
|
A | G | 1 | a0001c0001t0003g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.218-46A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114979460 | ||||||
| chr7:114979869
|
G | C | 3 | a0001c0001t0002g0050a0001c0001t0009g0108a0001c0001t0009g0125 | 3 | HG01361.hp2 HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.493+88G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114979869 | ||||||
| chr7:114979874
|
T | C | 1 | a0001c0001t0052g0209 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.493+93T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114979874 | ||||||
| chr7:114980027
|
G | A | 1 | a0001c0001t0003g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.493+246G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114980027 | ||||||
| chr7:114980091
|
A | T | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.493+310A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114980091 | ||||||
| chr7:114980451
|
C | T | 12 | a0001c0001t0002g0186a0001c0001t0007g0034a0001c0001t0007g0035others(9): Show | 13 | HG00738.hp2 HG01069.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.493+670C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114980451 | ||||||
| chr7:114980575
|
T | TA | 9 | a0001c0001t0001g0007a0001c0001t0022g0053a0001c0001t0022g0054others(6): Show | 10 | HG02280.hp1 HG02615.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.493+799dupA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114980575 | |||||
| chr7:114981137
|
C | T | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.493+1356C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114981137 | ||||||
| chr7:114981396
|
C | T | 1 | a0001c0001t0003g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.493+1615C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114981396 | ||||||
| chr7:114981405
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(105): Show | 114 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.493+1624G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114981405 | ||||||
| chr7:114981572
|
C | G | 1 | a0001c0001t0010g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+1791C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114981572 | ||||||
| chr7:114981588
|
A | T | 2 | a0001c0001t0012g0022a0001c0001t0033g0105 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.493+1807A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114981588 | ||||||
| chr7:114981732
|
G | A | 1 | a0001c0001t0004g0255 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.493+1951G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114981732 | ||||||
| chr7:114982037
|
G | T | 2 | a0001c0001t0048g0038a0001c0001t0065g0312 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.493+2256G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982037 | ||||||
| chr7:114982467
|
A | T | 1 | a0001c0001t0009g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.493+2686A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982467 | ||||||
| chr7:114982470
|
G | A | 13 | a0001c0001t0001g0115a0001c0001t0002g0186a0001c0001t0002g0203others(10): Show | 14 | HG00738.hp2 HG01106.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.493+2689G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982470 | ||||||
| chr7:114982504
|
A | G | 175 | a0001c0001t0001g0182a0001c0001t0001g0189a0001c0001t0001g0192others(172): Show | 182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.493+2723A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982504 | ||||||
| chr7:114982658
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0032g0113 | 2 | NA18969.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.493+2877A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982658 | ||||||
| chr7:114982725
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.493+2944A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982725 | ||||||
| chr7:114982809
|
G | A | 36 | a0001c0001t0002g0014a0001c0001t0002g0033a0001c0001t0002g0062others(33): Show | 38 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.493+3028G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982809 | ||||||
| chr7:114982910
|
C | T | 2 | a0001c0001t0006g0098a0001c0001t0007g0274 | 2 | HG01358.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.493+3129C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982910 | ||||||
| chr7:114982920
|
C | G | 4 | a0001c0001t0001g0007a0001c0001t0022g0053a0001c0001t0022g0054others(1): Show | 5 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+3139C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982920 | ||||||
| chr7:114982951
|
C | T | 2 | a0001c0001t0012g0022a0001c0001t0033g0105 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.493+3170C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982951 | ||||||
| chr7:114983283
|
G | A | 318 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(315): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.493+3502G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983283 | ||||||
| chr7:114983308
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(113): Show | 123 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.493+3527T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983308 | ||||||
| chr7:114983387
|
G | A | 2 | a0001c0001t0017g0006a0001c0001t0019g0006 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.493+3606G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983387 | ||||||
| chr7:114983452
|
G | A | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.493+3671G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983452 | ||||||
| chr7:114983503
|
T | G | 2 | a0001c0001t0022g0053a0001c0001t0022g0054 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.493+3722T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983503 | ||||||
| chr7:114983511
|
A | G | 104 | a0001c0001t0001g0182a0001c0001t0001g0189a0001c0001t0001g0192others(101): Show | 108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.493+3730A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983511 | ||||||
| chr7:114983514
|
G | A | 3 | a0001c0001t0003g0167a0001c0001t0003g0221a0001c0001t0003g0254 | 3 | HG00323.hp2 HG01081.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.493+3733G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983514 | ||||||
| chr7:114983563
|
C | CT | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(119): Show | 130 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.493+3804dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114983563 | |||||
| chr7:114983563
|
C | CTT | 93 | a0001c0001t0001g0063a0001c0001t0001g0130a0001c0001t0001g0150others(90): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.493+3803_493+3804d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114983563 | |||||
| chr7:114983563
|
C | CTTT | 11 | a0001c0001t0001g0182a0001c0001t0002g0047a0001c0001t0002g0060others(8): Show | 11 | HG00280.hp1 HG01175.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.493+3802_493+3804d others(5): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114983563 | |||||
| chr7:114983636
|
C | T | 1 | a0001c0001t0006g0245 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.493+3855C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983636 | ||||||
| chr7:114983687
|
C | T | 4 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0216others(1): Show | 4 | HG01928.hp2 HG01943.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+3906C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983687 | ||||||
| chr7:114983713
|
G | A | 1 | a0001c0002t0023g0169 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.493+3932G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983713 | ||||||
| chr7:114983725
|
G | A | 1 | a0001c0001t0005g0148 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.493+3944G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983725 | ||||||
| chr7:114983764
|
T | A | 2 | a0001c0001t0059g0307a0001c0003t0031g0019 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.493+3983T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983764 | ||||||
| chr7:114983861
|
A | G | 2 | a0001c0001t0059g0307a0001c0003t0031g0019 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.493+4080A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983861 | ||||||
| chr7:114983929
|
C | T | 2 | a0001c0001t0012g0022a0001c0001t0033g0105 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.493+4148C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983929 | ||||||
| chr7:114983973
|
A | T | 1 | a0001c0001t0005g0194 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.493+4192A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983973 | ||||||
| chr7:114984074
|
T | C | 6 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(3): Show | 6 | HG01099.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.493+4293T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984074 | ||||||
| chr7:114984089
|
C | T | 8 | a0001c0001t0005g0012a0001c0001t0005g0148a0001c0001t0005g0160others(5): Show | 8 | HG01256.hp2 HG01358.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.493+4308C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984089 | ||||||
| chr7:114984115
|
A | G | 4 | a0001c0001t0007g0017a0001c0001t0007g0274a0001c0001t0007g0275others(1): Show | 5 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+4334A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984115 | ||||||
| chr7:114984475
|
A | C | 2 | a0001c0001t0012g0022a0001c0001t0033g0105 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.493+4694A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984475 | ||||||
| chr7:114984547
|
T | A | 1 | a0001c0001t0018g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.493+4766T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984547 | ||||||
| chr7:114984625
|
C | A | 3 | a0001c0001t0007g0211a0001c0001t0007g0229a0001c0001t0007g0259 | 3 | HG00140.hp2 HG00741.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.493+4844C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984625 | ||||||
| chr7:114984674
|
C | T | 2 | a0001c0001t0005g0137a0001c0001t0005g0138 | 2 | NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.493+4893C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984674 | ||||||
| chr7:114984713
|
A | G | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+4932A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984713 | ||||||
| chr7:114984718
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(123): Show | 133 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.493+4937G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984718 | ||||||
| chr7:114984839
|
C | A | 1 | a0001c0001t0024g0257 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.493+5058C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984839 | ||||||
| chr7:114985111
|
C | T | 2 | a0001c0001t0060g0023a0001c0001t0061g0028 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.493+5330C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985111 | ||||||
| chr7:114985145
|
G | C | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.493+5364G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985145 | ||||||
| chr7:114985171
|
G | A | 1 | a0001c0001t0002g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.493+5390G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985171 | ||||||
| chr7:114985291
|
T | A | 59 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(56): Show | 62 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.493+5510T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985291 | ||||||
| chr7:114985367
|
A | G | 1 | a0001c0003t0036g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.493+5586A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985367 | ||||||
| chr7:114985482
|
C | G | 79 | a0001c0001t0001g0195a0001c0001t0001g0206a0001c0001t0001g0207others(76): Show | 83 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.493+5701C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985482 | ||||||
| chr7:114985484
|
G | C | 2 | a0001c0001t0002g0046a0001c0001t0002g0248 | 2 | HG01433.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.493+5703G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985484 | ||||||
| chr7:114985554
|
G | T | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+5773G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985554 | ||||||
| chr7:114985599
|
T | G | 1 | a0001c0001t0011g0073 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.493+5818T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985599 | ||||||
| chr7:114985659
|
T | C | 15 | a0001c0001t0001g0115a0001c0001t0002g0186a0001c0001t0002g0203others(12): Show | 16 | HG00738.hp2 HG01106.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.493+5878T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985659 | ||||||
| chr7:114985719
|
A | G | 1 | a0001c0001t0003g0214 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.493+5938A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985719 | ||||||
| chr7:114985734
|
G | T | 16 | a0001c0001t0001g0189a0001c0001t0004g0162a0001c0001t0004g0185others(13): Show | 16 | HG00323.hp1 HG00408.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.493+5953G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985734 | ||||||
| chr7:114986032
|
G | GT | 76 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0195others(73): Show | 81 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.493+6266dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114986032 | |||||
| chr7:114986032
|
GT | G | 90 | a0001c0001t0001g0070a0001c0001t0001g0189a0001c0001t0002g0002others(87): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.493+6266delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114986032 | |||||
| chr7:114986032
|
GTT | G | 29 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+6265_493+6266d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114986032 | |||||
| chr7:114986202
|
T | C | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+6421T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986202 | ||||||
| chr7:114986262
|
C | T | 75 | a0001c0001t0001g0195a0001c0001t0001g0206a0001c0001t0001g0207others(72): Show | 79 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+6481C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986262 | ||||||
| chr7:114986274
|
T | G | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.493+6493T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986274 | ||||||
| chr7:114986294
|
C | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(124): Show | 134 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.493+6513C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986294 | ||||||
| chr7:114986385
|
A | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(294): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.493+6604A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986385 | ||||||
| chr7:114986648
|
GTT | G | 28 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.493+6869_493+6870d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114986648 | |||||
| chr7:114986825
|
T | C | 29 | a0001c0001t0001g0182a0001c0001t0001g0192a0001c0001t0002g0074others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+7044T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986825 | ||||||
| chr7:114986848
|
G | A | 1 | a0001c0001t0004g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.493+7067G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986848 | ||||||
| chr7:114987043
|
A | G | 3 | a0001c0001t0003g0202a0001c0001t0003g0279a0001c0001t0003g0280 | 3 | HG01891.hp2 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.493+7262A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987043 | ||||||
| chr7:114987139
|
A | G | 75 | a0001c0001t0001g0195a0001c0001t0001g0206a0001c0001t0001g0207others(72): Show | 79 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+7358A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987139 | ||||||
| chr7:114987209
|
G | A | 1 | a0001c0001t0006g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.493+7428G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987209 | ||||||
| chr7:114987529
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.493+7748G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987529 | ||||||
| chr7:114987592
|
A | G | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+7811A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987592 | ||||||
| chr7:114987804
|
T | A | 5 | a0001c0001t0037g0041a0001c0001t0050g0061a0001c0001t0059g0307others(2): Show | 5 | HG01099.hp2 HG02280.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+8023T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987804 | ||||||
| chr7:114987845
|
G | C | 2 | a0001c0001t0014g0107a0001c0001t0014g0273 | 2 | HG00621.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.493+8064G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987845 | ||||||
| chr7:114987929
|
A | G | 2 | a0001c0001t0060g0023a0001c0001t0061g0028 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.493+8148A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987929 | ||||||
| chr7:114988064
|
T | G | 2 | a0001c0001t0019g0243a0001c0001t0019g0278 | 2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.493+8283T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114988064 | ||||||
| chr7:114988210
|
A | G | 314 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(311): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.493+8429A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114988210 | ||||||
| chr7:114988437
|
C | A | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.493+8656C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114988437 | ||||||
| chr7:114988464
|
C | T | 1 | a0001c0001t0029g0311 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.493+8683C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114988464 | ||||||
| chr7:114988667
|
TAGG | T | 3 | a0001c0001t0022g0053a0001c0001t0022g0054a0001c0001t0022g0055 | 3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.493+8891_493+8893d others(5): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114988667 | |||||
| chr7:114989057
|
G | A | 1 | a0001c0001t0063g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.493+9276G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989057 | ||||||
| chr7:114989064
|
G | A | 1 | a0001c0001t0004g0208 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.493+9283G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989064 | ||||||
| chr7:114989080
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.493+9299A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989080 | ||||||
| chr7:114989155
|
G | T | 3 | a0001c0001t0022g0053a0001c0001t0022g0054a0001c0001t0022g0055 | 3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.493+9374G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989155 | ||||||
| chr7:114989231
|
G | A | 58 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.493+9450G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989231 | ||||||
| chr7:114989290
|
G | A | 1 | a0001c0001t0033g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.493+9509G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989290 | ||||||
| chr7:114989642
|
T | C | 1 | a0001c0001t0027g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.493+9861T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989642 | ||||||
| chr7:114989665
|
C | A | 1 | a0001c0001t0037g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.493+9884C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989665 | ||||||
| chr7:114989769
|
G | A | 1 | a0001c0001t0004g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.493+9988G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989769 | ||||||
| chr7:114990103
|
A | G | 1 | a0001c0001t0010g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+10322A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990103 | ||||||
| chr7:114990193
|
T | A | 2 | a0001c0001t0011g0132a0001c0001t0011g0133 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.493+10412T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990193 | ||||||
| chr7:114990357
|
T | C | 2 | a0001c0001t0060g0023a0001c0001t0061g0028 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.493+10576T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990357 | ||||||
| chr7:114990483
|
A | C | 1 | a0001c0001t0003g0237 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.493+10702A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990483 | ||||||
| chr7:114990498
|
C | T | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+10717C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990498 | ||||||
| chr7:114990552
|
A | G | 3 | a0001c0001t0033g0105a0001c0001t0048g0038a0001c0001t0065g0312 | 3 | HG02258.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.493+10771A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990552 | ||||||
| chr7:114990583
|
G | T | 1 | a0001c0001t0003g0198 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.493+10802G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990583 | ||||||
| chr7:114990603
|
G | T | 29 | a0001c0001t0001g0182a0001c0001t0002g0074a0001c0001t0007g0017others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+10822G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990603 | ||||||
| chr7:114990669
|
G | A | 10 | a0001c0001t0001g0115a0001c0001t0002g0203a0001c0001t0008g0009others(7): Show | 11 | HG00738.hp2 HG01106.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.493+10888G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990669 | ||||||
| chr7:114990683
|
C | A | 1 | a0001c0001t0010g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.493+10902C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990683 | ||||||
| chr7:114990695
|
T | G | 1 | a0001c0001t0010g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+10914T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990695 | ||||||
| chr7:114990755
|
G | A | 1 | a0001c0003t0036g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.493+10974G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990755 | ||||||
| chr7:114990816
|
C | T | 5 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0071others(2): Show | 5 | HG02523.hp2 NA18940.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+11035C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990816 | ||||||
| chr7:114990842
|
A | G | 1 | a0001c0001t0004g0285 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.493+11061A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990842 | ||||||
| chr7:114990929
|
T | C | 314 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(311): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.493+11148T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990929 | ||||||
| chr7:114991002
|
T | C | 153 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0206others(150): Show | 160 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.493+11221T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991002 | ||||||
| chr7:114991007
|
C | A | 1 | a0001c0001t0018g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.493+11226C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991007 | ||||||
| chr7:114991007
|
C | T | 152 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0206others(149): Show | 159 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.493+11226C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991007 | ||||||
| chr7:114991046
|
T | C | 1 | a0001c0001t0004g0011 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.493+11265T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991046 | ||||||
| chr7:114991095
|
G | A | 1 | a0001c0001t0033g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.493+11314G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991095 | ||||||
| chr7:114991142
|
G | A | 1 | a0001c0001t0057g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.493+11361G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991142 | ||||||
| chr7:114991176
|
G | A | 1 | a0001c0001t0028g0292 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.493+11395G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991176 | ||||||
| chr7:114991250
|
T | C | 58 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.493+11469T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991250 | ||||||
| chr7:114991357
|
G | C | 1 | a0001c0001t0016g0075 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.493+11576G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991357 | ||||||
| chr7:114991455
|
T | G | 1 | a0001c0001t0003g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.493+11674T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991455 | ||||||
| chr7:114991705
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(113): Show | 123 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.493+11924C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991705 | ||||||
| chr7:114991708
|
T | C | 153 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0206others(150): Show | 160 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.493+11927T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991708 | ||||||
| chr7:114991738
|
T | G | 29 | a0001c0001t0001g0182a0001c0001t0002g0074a0001c0001t0007g0017others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+11957T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991738 | ||||||
| chr7:114991979
|
T | G | 1 | a0001c0001t0016g0239 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.493+12198T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991979 | ||||||
| chr7:114992010
|
T | C | 1 | a0001c0001t0024g0178 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.493+12229T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992010 | ||||||
| chr7:114992034
|
G | C | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+12253G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992034 | ||||||
| chr7:114992077
|
G | A | 1 | a0001c0001t0011g0193 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.493+12296G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992077 | ||||||
| chr7:114992123
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(97): Show | 106 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.493+12342G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992123 | ||||||
| chr7:114992287
|
A | T | 1 | a0001c0001t0018g0110 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.493+12506A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992287 | ||||||
| chr7:114992329
|
A | T | 1 | a0001c0001t0001g0153 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.493+12548A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992329 | ||||||
| chr7:114992382
|
CTA | C | 313 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(310): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.493+12603_493+1260 others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114992382 | |||||
| chr7:114992431
|
T | A | 1 | a0001c0001t0044g0106 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.493+12650T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992431 | ||||||
| chr7:114992445
|
C | T | 28 | a0001c0001t0001g0182a0001c0001t0002g0074a0001c0001t0007g0017others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.493+12664C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992445 | ||||||
| chr7:114992637
|
A | C | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.493+12856A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992637 | ||||||
| chr7:114992652
|
T | C | 2 | a0001c0001t0002g0046a0001c0001t0002g0248 | 2 | HG01433.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.493+12871T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992652 | ||||||
| chr7:114992752
|
A | G | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.493+12971A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992752 | ||||||
| chr7:114992832
|
A | C | 2 | a0001c0001t0003g0237a0001c0001t0003g0238 | 2 | NA18977.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.493+13051A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992832 | ||||||
| chr7:114992839
|
G | C | 4 | a0001c0001t0007g0017a0001c0001t0007g0274a0001c0001t0007g0275others(1): Show | 5 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+13058G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992839 | ||||||
| chr7:114992865
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(53): Show | 60 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.493+13084A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992865 | ||||||
| chr7:114992987
|
T | G | 74 | a0001c0001t0001g0195a0001c0001t0001g0206a0001c0001t0001g0207others(71): Show | 78 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.493+13206T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992987 | ||||||
| chr7:114992999
|
T | C | 28 | a0001c0001t0001g0182a0001c0001t0002g0074a0001c0001t0007g0017others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.493+13218T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992999 | ||||||
| chr7:114993202
|
C | G | 3 | a0001c0001t0002g0033a0001c0001t0009g0008a0001c0001t0017g0218 | 4 | HG01168.hp1 HG01169.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+13421C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993202 | ||||||
| chr7:114993266
|
C | T | 78 | a0001c0001t0001g0195a0001c0001t0001g0206a0001c0001t0001g0207others(75): Show | 82 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.493+13485C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993266 | ||||||
| chr7:114993508
|
A | G | 16 | a0001c0001t0001g0189a0001c0001t0004g0162a0001c0001t0004g0185others(13): Show | 16 | HG00323.hp1 HG00408.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.493+13727A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993508 | ||||||
| chr7:114993517
|
T | G | 1 | a0001c0001t0053g0076 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.493+13736T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993517 | ||||||
| chr7:114993728
|
T | C | 1 | a0001c0001t0010g0231 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.493+13947T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993728 | ||||||
| chr7:114993795
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(113): Show | 123 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.493+14014C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993795 | ||||||
| chr7:114993801
|
G | C | 23 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(20): Show | 24 | HG01243.hp1 HG01361.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.493+14020G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993801 | ||||||
| chr7:114993815
|
T | G | 1 | a0001c0001t0008g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.493+14034T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993815 | ||||||
| chr7:114994004
|
A | T | 2 | a0001c0001t0001g0004a0001c0001t0014g0004 | 3 | HG00673.hp1 HG02040.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.493+14223A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994004 | ||||||
| chr7:114994050
|
A | G | 1 | a0001c0001t0013g0282 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.493+14269A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994050 | ||||||
| chr7:114994103
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.493+14322A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994103 | ||||||
| chr7:114994112
|
T | G | 1 | a0001c0001t0024g0149 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.493+14331T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994112 | ||||||
| chr7:114994266
|
T | G | 29 | a0001c0001t0001g0182a0001c0001t0002g0074a0001c0001t0007g0017others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+14485T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994266 | ||||||
| chr7:114994275
|
C | CAATACAA others(11): Show |
3 | a0001c0001t0009g0124a0001c0001t0025g0118a0001c0001t0063g0117 | 3 | HG01978.hp1 HG03490.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.493+14495_493+1449 others(22): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114994275 | |||||
| chr7:114994277
|
C | G | 3 | a0001c0001t0009g0124a0001c0001t0025g0118a0001c0001t0063g0117 | 3 | HG01978.hp1 HG03490.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.493+14496C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994277 | ||||||
| chr7:114994405
|
G | A | 4 | a0001c0001t0010g0030a0001c0001t0012g0022a0001c0001t0041g0056others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+14624G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994405 | ||||||
| chr7:114994668
|
A | G | 1 | a0001c0001t0004g0277 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.493+14887A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994668 | ||||||
| chr7:114994686
|
C | A | 6 | a0001c0001t0010g0030a0001c0001t0010g0057a0001c0001t0012g0022others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.493+14905C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994686 | ||||||
| chr7:114994709
|
G | A | 2 | a0001c0001t0048g0038a0001c0001t0065g0312 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.493+14928G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994709 | ||||||
| chr7:114994775
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.493+14994C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994775 | ||||||
| chr7:114994967
|
T | C | 1 | a0001c0001t0005g0129 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.493+15186T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994967 | ||||||
| chr7:114994968
|
G | A | 1 | a0001c0001t0005g0129 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.493+15187G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994968 | ||||||
| chr7:114995057
|
A | G | 22 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(19): Show | 23 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.493+15276A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995057 | ||||||
| chr7:114995104
|
C | T | 1 | a0001c0003t0036g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.493+15323C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995104 | ||||||
| chr7:114995111
|
T | G | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.493+15330T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995111 | ||||||
| chr7:114995270
|
A | G | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+15489A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995270 | ||||||
| chr7:114995323
|
G | A | 3 | a0001c0001t0033g0105a0001c0001t0048g0038a0001c0001t0065g0312 | 3 | HG02258.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.493+15542G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995323 | ||||||
| chr7:114995329
|
A | T | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+15548A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995329 | ||||||
| chr7:114995348
|
G | A | 1 | a0001c0001t0034g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.493+15567G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995348 | ||||||
| chr7:114995388
|
G | A | 35 | a0001c0001t0003g0077a0001c0001t0003g0100a0001c0001t0003g0167others(32): Show | 37 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.493+15607G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995388 | ||||||
| chr7:114995406
|
G | C | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+15625G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995406 | ||||||
| chr7:114995425
|
G | T | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.493+15644G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995425 | ||||||
| chr7:114995483
|
C | A | 152 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0206others(149): Show | 159 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.493+15702C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995483 | ||||||
| chr7:114995564
|
G | T | 1 | a0001c0001t0001g0150 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.493+15783G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995564 | ||||||
| chr7:114995755
|
A | C | 2 | a0001c0001t0019g0243a0001c0001t0019g0278 | 2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.493+15974A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995755 | ||||||
| chr7:114995755
|
A | T | 23 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(20): Show | 24 | HG01243.hp1 HG01361.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.493+15974A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995755 | ||||||
| chr7:114995874
|
G | A | 2 | a0001c0001t0059g0307a0001c0003t0031g0019 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.493+16093G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995874 | ||||||
| chr7:114995905
|
A | C | 1 | a0001c0001t0011g0036 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.493+16124A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995905 | ||||||
| chr7:114995943
|
T | C | 314 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(311): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.493+16162T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995943 | ||||||
| chr7:114996421
|
T | C | 35 | a0001c0001t0003g0077a0001c0001t0003g0100a0001c0001t0003g0167others(32): Show | 37 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.493+16640T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996421 | ||||||
| chr7:114996427
|
G | T | 2 | a0001c0001t0008g0037a0001c0001t0044g0106 | 2 | HG01168.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.493+16646G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996427 | ||||||
| chr7:114996555
|
G | A | 1 | a0001c0001t0037g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.493+16774G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996555 | ||||||
| chr7:114996602
|
G | A | 1 | a0001c0001t0012g0139 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.493+16821G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996602 | ||||||
| chr7:114996652
|
G | A | 2 | a0001c0001t0060g0023a0001c0001t0061g0028 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.493+16871G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996652 | ||||||
| chr7:114996695
|
A | C | 28 | a0001c0001t0001g0182a0001c0001t0002g0074a0001c0001t0007g0017others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.493+16914A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996695 | ||||||
| chr7:114996771
|
G | A | 1 | a0001c0001t0033g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.493+16990G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996771 | ||||||
| chr7:114996813
|
G | A | 1 | a0001c0001t0009g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.493+17032G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996813 | ||||||
| chr7:114996897
|
A | T | 16 | a0001c0001t0001g0115a0001c0001t0002g0203a0001c0001t0007g0268others(13): Show | 17 | HG00738.hp2 HG01106.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.493+17116A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996897 | ||||||
| chr7:114996962
|
C | A | 1 | a0001c0001t0033g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.493+17181C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996962 | ||||||
| chr7:114997009
|
T | C | 1 | a0001c0001t0003g0214 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.493+17228T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997009 | ||||||
| chr7:114997015
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.493+17234G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997015 | ||||||
| chr7:114997400
|
A | G | 1 | a0001c0001t0003g0170 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.493+17619A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997400 | ||||||
| chr7:114997408
|
A | ATG | 6 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0002g0228others(3): Show | 6 | HG00280.hp2 HG02818.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.493+17644_493+1764 others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114997408 | |||||
| chr7:114997425
|
T | C | 1 | a0001c0001t0033g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.493+17644T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997425 | ||||||
| chr7:114997521
|
G | A | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+17740G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997521 | ||||||
| chr7:114997576
|
GA | G | 184 | a0001c0001t0001g0182a0001c0001t0001g0195a0001c0001t0001g0206others(181): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.493+17812delA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114997576 | |||||
| chr7:114997576
|
GAA | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(97): Show | 106 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.493+17811_493+1781 others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114997576 | |||||
| chr7:114997734
|
T | C | 2 | a0001c0001t0048g0038a0001c0001t0065g0312 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.493+17953T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997734 | ||||||
| chr7:114997773
|
G | T | 74 | a0001c0001t0001g0195a0001c0001t0001g0206a0001c0001t0001g0207others(71): Show | 78 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.494-17915G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997773 | ||||||
| chr7:114997838
|
G | T | 2 | a0001c0001t0022g0053a0001c0001t0022g0054 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.494-17850G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997838 | ||||||
| chr7:114997849
|
G | A | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494-17839G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997849 | ||||||
| chr7:114998025
|
A | T | 1 | a0001c0003t0036g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.494-17663A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998025 | ||||||
| chr7:114998026
|
C | T | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494-17662C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998026 | ||||||
| chr7:114998105
|
A | C | 1 | a0001c0001t0002g0230 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.494-17583A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998105 | ||||||
| chr7:114998135
|
G | A | 1 | a0001c0001t0010g0084 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.494-17553G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998135 | ||||||
| chr7:114998276
|
G | A | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494-17412G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998276 | ||||||
| chr7:114998328
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0082 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.494-17360G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998328 | ||||||
| chr7:114998469
|
A | G | 2 | a0001c0001t0060g0023a0001c0001t0061g0028 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.494-17219A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998469 | ||||||
| chr7:114998483
|
T | A | 4 | a0001c0001t0018g0005a0001c0001t0018g0099a0001c0001t0018g0110others(1): Show | 5 | HG02135.hp1 NA18963.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-17205T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998483 | ||||||
| chr7:114998681
|
T | C | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.494-17007T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998681 | ||||||
| chr7:114998832
|
G | A | 6 | a0001c0001t0010g0030a0001c0001t0010g0057a0001c0001t0012g0022others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.494-16856G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998832 | ||||||
| chr7:114998923
|
T | C | 35 | a0001c0001t0003g0077a0001c0001t0003g0100a0001c0001t0003g0167others(32): Show | 37 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.494-16765T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998923 | ||||||
| chr7:114999338
|
C | T | 314 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(311): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.494-16350C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999338 | ||||||
| chr7:114999391
|
C | T | 314 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(311): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.494-16297C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999391 | ||||||
| chr7:114999538
|
T | C | 16 | a0001c0001t0001g0189a0001c0001t0004g0162a0001c0001t0004g0185others(13): Show | 16 | HG00323.hp1 HG00408.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.494-16150T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999538 | ||||||
| chr7:114999583
|
A | G | 1 | a0001c0001t0009g0120 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.494-16105A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999583 | ||||||
| chr7:114999619
|
T | C | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.494-16069T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999619 | ||||||
| chr7:114999650
|
A | G | 1 | a0001c0001t0034g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.494-16038A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999650 | ||||||
| chr7:114999692
|
G | A | 301 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(298): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.494-15996G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999692 | ||||||
| chr7:114999779
|
C | CA | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(266): Show | 283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.494-15909_494-1590 others(5): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999779 | ||||||
| chr7:114999828
|
A | T | 3 | a0001c0001t0033g0105a0001c0001t0048g0038a0001c0001t0065g0312 | 3 | HG02258.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.494-15860A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999828 | ||||||
| chr7:114999840
|
A | C | 1 | a0001c0001t0010g0078 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.494-15848A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999840 | ||||||
| chr7:114999896
|
G | A | 3 | a0001c0001t0003g0100a0001c0001t0003g0214a0001c0001t0003g0217 | 3 | NA18972.hp1 NA19009.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.494-15792G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999896 | ||||||
| chr7:115000023
|
T | C | 1 | a0001c0001t0003g0236 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.494-15665T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000023 | ||||||
| chr7:115000184
|
A | C | 1 | a0001c0001t0033g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.494-15504A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000184 | ||||||
| chr7:115000263
|
G | C | 1 | a0001c0001t0015g0289 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.494-15425G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000263 | ||||||
| chr7:115000305
|
A | G | 153 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0206others(150): Show | 160 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.494-15383A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000305 | ||||||
| chr7:115000425
|
G | T | 1 | a0001c0001t0010g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494-15263G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000425 | ||||||
| chr7:115000505
|
G | A | 1 | a0001c0001t0033g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.494-15183G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000505 | ||||||
| chr7:115000524
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.494-15164A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000524 | ||||||
| chr7:115000553
|
C | T | 1 | a0001c0001t0004g0285 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.494-15135C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000553 | ||||||
| chr7:115000645
|
T | G | 2 | a0001c0001t0005g0137a0001c0001t0005g0138 | 2 | NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.494-15043T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000645 | ||||||
| chr7:115000660
|
G | T | 1 | a0001c0001t0021g0263 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.494-15028G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000660 | ||||||
| chr7:115000772
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(113): Show | 123 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.494-14916C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000772 | ||||||
| chr7:115001017
|
C | T | 1 | a0001c0001t0033g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.494-14671C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115001017 | ||||||
| chr7:115001287
|
T | A | 1 | a0001c0001t0008g0116 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.494-14401T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115001287 | ||||||
| chr7:115001323
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.494-14365C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115001323 | ||||||
| chr7:115001445
|
T | C | 2 | a0001c0001t0040g0136a0001c0001t0062g0119 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.494-14243T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115001445 | ||||||
| chr7:115001720
|
A | AT | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(113): Show | 123 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.494-13962dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115001720 | |||||
| chr7:115001939
|
C | T | 16 | a0001c0001t0001g0189a0001c0001t0004g0162a0001c0001t0004g0185others(13): Show | 16 | HG00323.hp1 HG00408.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.494-13749C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115001939 | ||||||
| chr7:115002078
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.494-13610C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002078 | ||||||
| chr7:115002146
|
AAAACAAA others(1): Show |
A | 74 | a0001c0001t0001g0195a0001c0001t0001g0206a0001c0001t0001g0207others(71): Show | 78 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.494-13526_494-1351 others(12): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115002146 | |||||
| chr7:115002204
|
T | C | 6 | a0001c0001t0010g0030a0001c0001t0010g0057a0001c0001t0012g0022others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.494-13484T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002204 | ||||||
| chr7:115002265
|
C | T | 1 | a0001c0001t0016g0244 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.494-13423C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002265 | ||||||
| chr7:115002466
|
T | A | 3 | a0001c0001t0033g0105a0001c0001t0048g0038a0001c0001t0065g0312 | 3 | HG02258.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.494-13222T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002466 | ||||||
| chr7:115002577
|
G | C | 2 | a0001c0001t0002g0074a0001c0001t0011g0073 | 2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.494-13111G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002577 | ||||||
| chr7:115002797
|
T | C | 3 | a0001c0001t0009g0124a0001c0001t0025g0118a0001c0001t0063g0117 | 3 | HG01978.hp1 HG03490.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.494-12891T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002797 | ||||||
| chr7:115002852
|
T | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | NA18982.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.494-12836T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002852 | ||||||
| chr7:115002863
|
T | C | 313 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(310): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.494-12825T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002863 | ||||||
| chr7:115002874
|
A | G | 152 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0206others(149): Show | 159 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.494-12814A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002874 | ||||||
| chr7:115002876
|
A | G | 2 | a0001c0001t0059g0307a0001c0003t0031g0019 | 2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.494-12812A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002876 | ||||||
| chr7:115003055
|
C | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(297): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.494-12633C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003055 | ||||||
| chr7:115003252
|
T | A | 58 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.494-12436T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003252 | ||||||
| chr7:115003319
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.494-12369G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003319 | ||||||
| chr7:115003474
|
G | A | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.494-12214G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003474 | ||||||
| chr7:115003476
|
T | C | 1 | a0001c0006t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.494-12212T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003476 | ||||||
| chr7:115003584
|
A | G | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.494-12104A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003584 | ||||||
| chr7:115003649
|
T | C | 4 | a0001c0001t0007g0017a0001c0001t0007g0274a0001c0001t0007g0275others(1): Show | 5 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-12039T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003649 | ||||||
| chr7:115003810
|
T | G | 1 | a0001c0001t0033g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.494-11878T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003810 | ||||||
| chr7:115003874
|
G | A | 152 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0206others(149): Show | 159 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.494-11814G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003874 | ||||||
| chr7:115003904
|
C | T | 58 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(55): Show | 61 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.494-11784C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003904 | ||||||
| chr7:115004139
|
C | T | 1 | a0001c0001t0011g0193 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.494-11549C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115004139 | ||||||
| chr7:115004233
|
G | C | 1 | a0001c0001t0004g0242 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.494-11455G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115004233 | ||||||
| chr7:115004403
|
A | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(97): Show | 106 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.494-11285A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115004403 | ||||||
| chr7:115004432
|
A | C | 1 | a0001c0001t0004g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.494-11256A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115004432 | ||||||
| chr7:115004637
|
C | T | 1 | a0001c0001t0017g0204 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.494-11051C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115004637 | ||||||
| chr7:115004987
|
C | T | 1 | a0001c0001t0004g0258 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.494-10701C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115004987 | ||||||
| chr7:115005189
|
A | G | 1 | a0001c0001t0046g0156 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.494-10499A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115005189 | ||||||
| chr7:115005252
|
G | C | 2 | a0001c0001t0048g0038a0001c0001t0065g0312 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.494-10436G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115005252 | ||||||
| chr7:115005328
|
ATTAATTG others(57): Show |
A | 1 | a0001c0003t0043g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.494-10355_494-1029 others(68): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115005328 | |||||
| chr7:115005593
|
A | G | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.494-10095A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115005593 | ||||||
| chr7:115005718
|
A | T | 1 | a0001c0001t0006g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.494-9970A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115005718 | ||||||
| chr7:115005990
|
C | T | 1 | a0001c0001t0037g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.494-9698C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115005990 | ||||||
| chr7:115006060
|
G | A | 28 | a0001c0001t0001g0182a0001c0001t0002g0074a0001c0001t0007g0017others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.494-9628G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006060 | ||||||
| chr7:115006114
|
T | C | 12 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(9): Show | 13 | HG01361.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.494-9574T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006114 | ||||||
| chr7:115006164
|
C | T | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.494-9524C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006164 | ||||||
| chr7:115006295
|
A | T | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494-9393A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006295 | ||||||
| chr7:115006669
|
G | A | 313 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(310): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.494-9019G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006669 | ||||||
| chr7:115006683
|
A | G | 10 | a0001c0001t0010g0030a0001c0001t0010g0057a0001c0001t0012g0022others(7): Show | 10 | HG02258.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.494-9005A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006683 | ||||||
| chr7:115006935
|
G | GTTTTACT others(8): Show |
311 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(308): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.494-8750_494-8749i others(17): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115006935 | |||||
| chr7:115006977
|
A | T | 28 | a0001c0001t0001g0182a0001c0001t0002g0074a0001c0001t0007g0017others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.494-8711A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006977 | ||||||
| chr7:115007175
|
A | C | 1 | a0001c0001t0004g0271 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.494-8513A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007175 | ||||||
| chr7:115007362
|
G | T | 5 | a0001c0001t0001g0083a0001c0001t0001g0192a0001c0001t0026g0164others(2): Show | 5 | HG02015.hp2 HG02132.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-8326G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007362 | ||||||
| chr7:115007430
|
T | C | 1 | a0001c0001t0003g0254 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.494-8258T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007430 | ||||||
| chr7:115007506
|
T | C | 1 | a0001c0001t0042g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494-8182T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007506 | ||||||
| chr7:115007630
|
G | A | 2 | a0001c0001t0010g0057a0001c0001t0058g0252 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.494-8058G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007630 | ||||||
| chr7:115007630
|
G | GTA | 23 | a0001c0001t0001g0182a0001c0001t0002g0074a0001c0001t0002g0102others(20): Show | 24 | HG00140.hp2 HG00741.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.494-8032_494-8031d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | |||||
| chr7:115007630
|
G | GTATA | 9 | a0001c0001t0007g0157a0001c0001t0011g0036a0001c0001t0011g0073others(6): Show | 9 | HG01069.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.494-8034_494-8031d others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | |||||
| chr7:115007630
|
G | GTATATA | 3 | a0001c0001t0011g0168a0001c0001t0041g0056a0001c0001t0046g0156 | 3 | HG03098.hp1 HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.494-8036_494-8031d others(8): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | |||||
| chr7:115007630
|
G | GTATATAT others(1): Show |
3 | a0001c0001t0002g0044a0001c0001t0007g0035a0001c0001t0007g0172 | 3 | HG00099.hp1 HG02738.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.494-8038_494-8031d others(10): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | |||||
| chr7:115007630
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0007g0034 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.494-8042_494-8031d others(14): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | |||||
| chr7:115007630
|
G | GTGTATAT others(3): Show |
1 | a0001c0001t0061g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.494-8057_494-8056i others(12): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | |||||
| chr7:115007630
|
G | GTGTGTAT others(21): Show |
1 | a0001c0001t0022g0053 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.494-8057_494-8056i others(30): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | |||||
| chr7:115007630
|
G | GTGTGTAT others(27): Show |
1 | a0001c0001t0022g0054 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.494-8057_494-8056i others(36): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | |||||
| chr7:115007630
|
G | GTGTGTAT others(29): Show |
1 | a0001c0001t0022g0055 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.494-8057_494-8056i others(38): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | |||||
| chr7:115007630
|
GTATATAT others(5): Show |
G | 2 | a0001c0001t0004g0011a0001c0001t0004g0208 | 3 | HG01257.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.494-8042_494-8031d others(14): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | |||||
| chr7:115007630
|
GTATATAT others(7): Show |
G | 244 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(241): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.494-8044_494-8031d others(16): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | |||||
| chr7:115007806
|
C | T | 16 | a0001c0001t0001g0189a0001c0001t0004g0162a0001c0001t0004g0185others(13): Show | 16 | HG00323.hp1 HG00408.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.494-7882C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007806 | ||||||
| chr7:115007862
|
A | AT | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(132): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.494-7810dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007862 | |||||
| chr7:115007862
|
A | ATT | 12 | a0001c0001t0001g0115a0001c0001t0002g0203a0001c0001t0007g0276others(9): Show | 13 | HG01106.hp2 HG01175.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.494-7811_494-7810d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007862 | |||||
| chr7:115007940
|
G | T | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.494-7748G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007940 | ||||||
| chr7:115007987
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.494-7701C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007987 | ||||||
| chr7:115008011
|
C | T | 2 | a0001c0001t0060g0023a0001c0001t0061g0028 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.494-7677C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008011 | ||||||
| chr7:115008065
|
G | T | 315 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(312): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.494-7623G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008065 | ||||||
| chr7:115008169
|
C | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(205): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.494-7519C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008169 | ||||||
| chr7:115008199
|
G | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(277): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.494-7489G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008199 | ||||||
| chr7:115008212
|
A | C | 3 | a0001c0001t0020g0010a0001c0001t0020g0147a0001c0001t0020g0201 | 4 | HG01070.hp1 HG01071.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-7476A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008212 | ||||||
| chr7:115008523
|
C | T | 2 | a0001c0001t0048g0038a0001c0001t0065g0312 | 2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.494-7165C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008523 | ||||||
| chr7:115008608
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0248 | 2 | HG01433.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.494-7080C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008608 | ||||||
| chr7:115008779
|
G | T | 1 | a0001c0001t0057g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.494-6909G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008779 | ||||||
| chr7:115008874
|
G | A | 1 | a0001c0001t0008g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.494-6814G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008874 | ||||||
| chr7:115008895
|
C | G | 1 | a0001c0001t0002g0059 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.494-6793C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008895 | ||||||
| chr7:115009088
|
A | G | 1 | a0001c0001t0002g0266 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.494-6600A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115009088 | ||||||
| chr7:115009097
|
G | A | 2 | a0001c0001t0004g0242a0001c0001t0016g0075 | 2 | NA19085.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.494-6591G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115009097 | ||||||
| chr7:115009777
|
G | A | 7 | a0001c0001t0010g0030a0001c0001t0010g0057a0001c0001t0012g0022others(4): Show | 7 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-5911G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115009777 | ||||||
| chr7:115010064
|
CTTA | C | 23 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(20): Show | 24 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.494-5623_494-5621d others(5): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010064 | ||||||
| chr7:115010069
|
GA | G | 23 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(20): Show | 24 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.494-5617delA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115010069 | |||||
| chr7:115010071
|
A | T | 23 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(20): Show | 24 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.494-5617A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010071 | ||||||
| chr7:115010073
|
AGG | A | 23 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(20): Show | 24 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.494-5612_494-5611d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115010073 | |||||
| chr7:115010130
|
T | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0065others(22): Show | 28 | HG00609.hp1 HG02015.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.494-5558T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010130 | ||||||
| chr7:115010131
|
A | T | 1 | a0001c0001t0016g0239 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.494-5557A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010131 | ||||||
| chr7:115010547
|
T | G | 3 | a0001c0001t0022g0053a0001c0001t0022g0054a0001c0001t0022g0055 | 3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.494-5141T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010547 | ||||||
| chr7:115010763
|
C | T | 2 | a0001c0001t0002g0143a0001c0001t0002g0186 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.494-4925C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010763 | ||||||
| chr7:115010915
|
A | T | 3 | a0001c0001t0002g0228a0001c0001t0002g0251a0001c0001t0002g0266 | 3 | HG01192.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.494-4773A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010915 | ||||||
| chr7:115010977
|
A | G | 35 | a0001c0001t0003g0077a0001c0001t0003g0100a0001c0001t0003g0167others(32): Show | 37 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.494-4711A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010977 | ||||||
| chr7:115011178
|
A | G | 4 | a0001c0001t0011g0132a0001c0001t0011g0133a0001c0001t0040g0136others(1): Show | 4 | HG01891.hp1 HG02109.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-4510A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011178 | ||||||
| chr7:115011260
|
G | A | 1 | a0001c0001t0033g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.494-4428G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011260 | ||||||
| chr7:115011261
|
G | A | 2 | a0001c0001t0002g0143a0001c0001t0002g0186 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.494-4427G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011261 | ||||||
| chr7:115011602
|
A | G | 1 | a0001c0001t0004g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.494-4086A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011602 | ||||||
| chr7:115011640
|
A | G | 49 | a0001c0001t0004g0011a0001c0001t0004g0016a0001c0001t0004g0064others(46): Show | 52 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.494-4048A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011640 | ||||||
| chr7:115011697
|
CAT | C | 4 | a0001c0001t0058g0252a0001c0001t0059g0307a0001c0001t0060g0023others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-3990_494-3989d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011697 | ||||||
| chr7:115011876
|
C | T | 37 | a0001c0001t0004g0162a0001c0001t0005g0003a0001c0001t0005g0012others(34): Show | 38 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.494-3812C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011876 | ||||||
| chr7:115011877
|
G | A | 12 | a0001c0001t0002g0002a0001c0001t0002g0043a0001c0001t0002g0044others(9): Show | 13 | HG01361.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.494-3811G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011877 | ||||||
| chr7:115011916
|
A | C | 1 | a0001c0001t0002g0074 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.494-3772A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011916 | ||||||
| chr7:115012021
|
C | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0063others(55): Show | 62 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.494-3667C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115012021 | ||||||
| chr7:115012266
|
A | G | 1 | a0001c0001t0004g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.494-3422A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115012266 | ||||||
| chr7:115012379
|
G | A | 1 | a0001c0001t0041g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.494-3309G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115012379 | ||||||
| chr7:115012382
|
G | A | 4 | a0001c0001t0011g0132a0001c0001t0011g0133a0001c0001t0040g0136others(1): Show | 4 | HG01891.hp1 HG02109.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-3306G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115012382 | ||||||
| chr7:115012786
|
T | C | 1 | a0001c0001t0041g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.494-2902T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115012786 | ||||||
| chr7:115012935
|
C | T | 2 | a0001c0001t0007g0275a0001c0001t0050g0061 | 2 | HG01081.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.494-2753C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115012935 | ||||||
| chr7:115013321
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.494-2367G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115013321 | ||||||
| chr7:115013344
|
GA | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(176): Show | 189 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.494-2342delA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115013344 | |||||
| chr7:115013369
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.494-2319A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115013369 | ||||||
| chr7:115013389
|
A | G | 2 | a0001c0001t0006g0154a0001c0001t0054g0261 | 2 | NA19087.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.494-2299A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115013389 | ||||||
| chr7:115013415
|
G | A | 3 | a0001c0001t0022g0053a0001c0001t0022g0054a0001c0001t0022g0055 | 3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.494-2273G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115013415 | ||||||
| chr7:115013564
|
A | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(66): Show | 74 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.494-2124A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115013564 | ||||||
| chr7:115013985
|
C | T | 33 | a0001c0001t0007g0017a0001c0001t0007g0034a0001c0001t0007g0035others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.494-1703C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115013985 | ||||||
| chr7:115014045
|
C | A | 49 | a0001c0001t0004g0011a0001c0001t0004g0016a0001c0001t0004g0064others(46): Show | 52 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.494-1643C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014045 | ||||||
| chr7:115014085
|
T | G | 2 | a0001c0001t0004g0284a0001c0001t0006g0300 | 2 | NA18998.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.494-1603T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014085 | ||||||
| chr7:115014119
|
G | A | 1 | a0001c0001t0057g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.494-1569G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014119 | ||||||
| chr7:115014127
|
T | C | 1 | a0001c0001t0010g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.494-1561T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014127 | ||||||
| chr7:115014184
|
G | A | 2 | a0001c0001t0003g0213a0001c0001t0035g0205 | 2 | HG03654.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.494-1504G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014184 | ||||||
| chr7:115014274
|
G | T | 1 | a0001c0001t0058g0252 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.494-1414G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014274 | ||||||
| chr7:115014475
|
C | T | 1 | a0001c0001t0030g0069 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.494-1213C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014475 | ||||||
| chr7:115014484
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.494-1204G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014484 | ||||||
| chr7:115014488
|
T | C | 4 | a0001c0001t0008g0018a0001c0001t0008g0116a0001c0001t0008g0140others(1): Show | 4 | HG01496.hp2 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-1200T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014488 | ||||||
| chr7:115014541
|
G | T | 4 | a0001c0001t0028g0031a0001c0001t0028g0292a0001c0001t0029g0042others(1): Show | 4 | HG02738.hp1 HG03492.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-1147G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014541 | ||||||
| chr7:115014562
|
C | T | 1 | a0001c0001t0010g0084 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.494-1126C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014562 | ||||||
| chr7:115014628
|
C | A | 1 | a0001c0001t0011g0073 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.494-1060C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014628 | ||||||
| chr7:115014779
|
CT | C | 3 | a0001c0001t0022g0053a0001c0001t0022g0054a0001c0001t0022g0055 | 3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.494-908delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014779 | ||||||
| chr7:115014963
|
C | A | 1 | a0001c0001t0039g0152 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.494-725C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014963 | ||||||
| chr7:115015058
|
C | T | 1 | a0001c0001t0058g0252 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.494-630C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115015058 | ||||||
| chr7:115015314
|
A | C | 1 | a0001c0001t0014g0288 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.494-374A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115015314 |