| geneid | 23288 |
|---|---|
| ensemblid | ENSG00000106012.19 |
| hgncid | 29171 |
| symbol | IQCE |
| name | IQ motif containing E |
| refseq_nuc | NM_152558.5 |
| refseq_prot | NP_689771.3 |
| ensembl_nuc | ENST00000402050.7 |
| ensembl_prot | ENSP00000385597.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 2558979 |
| end | 2614728 |
| strand | + |
| ver | v1.2 |
| region | chr7:2558979-2614728 |
| region5000 | chr7:2553979-2619728 |
| regionname0 | IQCE_chr7_2558979_2614728 |
| regionname5000 | IQCE_chr7_2553979_2619728 |
| 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 | 1/0 | 695 | 175 | 39 | 33 | 70 | 9 | 23 | 54 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002 | 0/0 | 695 | 129 | 8 | 16 | 92 | 4 | 9 | 69 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003 | 0/1 | 695 | 34 | 4 | 14 | 12 | 1 | 2 | 11 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0004 | 0/0 | 695 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0005 | 0/0 | 695 | 10 | 0 | 7 | 0 | 2 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0006 | 0/0 | 695 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0007 | 0/0 | 695 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0008 | 0/0 | 695 | 10 | 7 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0009 | 0/0 | 695 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0010 | 0/0 | 695 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0011 | 0/0 | 695 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0012 | 0/0 | 695 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0013 | 0/0 | 695 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0014 | 0/0 | 695 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0015 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0016 | 0/0 | 695 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0017 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0018 | 0/0 | 695 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0019 | 0/0 | 695 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0020 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0021 | 0/0 | 695 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0022 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0023 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0024 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0025 | 0/0 | 695 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0026 | 0/0 | 695 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0027 | 0/0 | 695 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| 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 | 0/0 | 2088 | 104 | 14 | 18 | 51 | 5 | 16 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0002 | 0/0 | 2088 | 82 | 0 | 9 | 68 | 0 | 5 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0003 | 1/0 | 2088 | 50 | 14 | 10 | 19 | 2 | 4 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0004 | 0/0 | 2088 | 37 | 4 | 6 | 19 | 4 | 4 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0005 | 0/1 | 2088 | 30 | 1 | 14 | 11 | 1 | 2 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0006 | 0/0 | 2088 | 10 | 7 | 3 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0007 | 0/0 | 2088 | 10 | 0 | 7 | 0 | 2 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0008 | 0/0 | 2088 | 10 | 10 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0009 | 0/0 | 2088 | 7 | 6 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0010 | 0/0 | 2088 | 7 | 5 | 2 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0011 | 0/0 | 2088 | 5 | 2 | 1 | 0 | 1 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0012 | 0/0 | 2088 | 5 | 5 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0013 | 0/0 | 2088 | 4 | 4 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0014 | 0/0 | 2088 | 4 | 0 | 0 | 4 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0015 | 0/0 | 2088 | 3 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0016 | 0/0 | 2088 | 3 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0017 | 0/0 | 2088 | 2 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0018 | 0/0 | 2088 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0019 | 0/0 | 2088 | 2 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0020 | 0/0 | 2088 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0021 | 0/0 | 2088 | 2 | 0 | 0 | 0 | 0 | 2 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0022 | 0/0 | 2088 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0023 | 0/0 | 2088 | 2 | 0 | 0 | 2 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0024 | 0/0 | 2088 | 2 | 0 | 2 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0025 | 0/0 | 2088 | 2 | 1 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0026 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0027 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0028 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0029 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0030 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0031 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0032 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0033 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0034 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0035 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0036 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0037 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0038 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0039 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0040 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0041 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0042 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0043 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0044 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0045 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0046 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0047 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0048 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0049 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0050 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0051 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| c0052 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 4770 | 67 | 6 | 13 | 39 | 2 | 6 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0002 | 0/0 | 4787 | 49 | 5 | 7 | 33 | 0 | 4 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0003 | 0/0 | 4787 | 47 | 2 | 4 | 36 | 2 | 3 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0004 | 0/0 | 4770 | 22 | 1 | 4 | 16 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0005 | 0/0 | 4774 | 14 | 0 | 7 | 3 | 0 | 4 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0006 | 0/0 | 4774 | 11 | 0 | 3 | 2 | 2 | 4 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0007 | 0/0 | 4772 | 10 | 0 | 6 | 0 | 2 | 2 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0008 | 0/0 | 4782 | 8 | 0 | 8 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0009 | 0/0 | 4776 | 7 | 5 | 2 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0010 | 0/0 | 4775 | 7 | 7 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0011 | 0/0 | 4766 | 7 | 0 | 0 | 7 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0012 | 0/0 | 4787 | 5 | 0 | 0 | 5 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0013 | 0/0 | 4788 | 5 | 0 | 0 | 4 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0014 | 0/0 | 4784 | 5 | 4 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0015 | 0/0 | 4787 | 5 | 0 | 5 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0016 | 0/0 | 4771 | 4 | 0 | 2 | 1 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0017 | 0/0 | 4779 | 4 | 4 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0018 | 0/0 | 4787 | 4 | 0 | 0 | 4 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0019 | 0/0 | 4802 | 4 | 4 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0020 | 0/0 | 4805 | 3 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0021 | 0/0 | 4774 | 3 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0022 | 0/0 | 4775 | 3 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0023 | 0/0 | 4751 | 3 | 2 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0024 | 0/0 | 4766 | 3 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0025 | 0/1 | 4766 | 3 | 0 | 2 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0026 | 0/0 | 4765 | 3 | 2 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0027 | 0/0 | 4780 | 3 | 2 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0028 | 0/0 | 4775 | 2 | 0 | 0 | 2 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0029 | 0/0 | 4788 | 2 | 0 | 1 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0030 | 0/0 | 4805 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0031 | 0/0 | 4769 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0032 | 0/0 | 4774 | 2 | 0 | 0 | 0 | 2 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0033 | 0/0 | 4785 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0034 | 0/0 | 4780 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0035 | 0/0 | 4787 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0036 | 0/0 | 4803 | 2 | 0 | 0 | 0 | 1 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0037 | 0/0 | 4774 | 2 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0038 | 0/0 | 4774 | 2 | 0 | 0 | 1 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0039 | 0/0 | 4787 | 2 | 0 | 0 | 1 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0040 | 0/0 | 4787 | 2 | 0 | 0 | 0 | 0 | 2 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0041 | 0/0 | 4766 | 2 | 0 | 2 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0042 | 0/0 | 4766 | 2 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0043 | 0/0 | 4766 | 2 | 0 | 0 | 2 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0044 | 0/0 | 4788 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0045 | 0/0 | 4770 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0046 | 0/0 | 4767 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0047 | 0/0 | 4773 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0048 | 0/0 | 4771 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0049 | 0/0 | 4788 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0050 | 0/0 | 4788 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0051 | 0/0 | 4787 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0052 | 0/0 | 4765 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0053 | 0/0 | 4776 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0054 | 0/0 | 4774 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0055 | 0/0 | 4785 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0056 | 0/0 | 4774 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0057 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0058 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0059 | 0/0 | 4779 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0060 | 0/0 | 4779 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0061 | 0/0 | 4784 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0062 | 0/0 | 4784 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0063 | 0/0 | 4789 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0064 | 0/0 | 4775 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0065 | 0/0 | 4785 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0066 | 0/0 | 4785 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0067 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0068 | 0/0 | 4775 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0069 | 0/0 | 4779 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0070 | 0/0 | 4775 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0071 | 0/0 | 4770 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0072 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0073 | 0/0 | 4787 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0074 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0075 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0076 | 0/0 | 4771 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0077 | 0/0 | 4787 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0078 | 0/0 | 4789 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0079 | 0/0 | 4787 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0080 | 0/0 | 4787 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0081 | 0/0 | 4802 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0082 | 0/0 | 4751 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0083 | 0/0 | 4767 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0084 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0085 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0086 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0087 | 0/0 | 4782 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0088 | 0/0 | 4765 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0089 | 0/0 | 4772 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0090 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0091 | 0/0 | 4780 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0092 | 0/0 | 4779 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0093 | 0/0 | 4770 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0094 | 0/0 | 4803 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0095 | 0/0 | 4770 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0096 | 0/0 | 4770 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0097 | 0/0 | 4764 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0098 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0099 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0100 | 0/0 | 4779 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0101 | 0/0 | 4779 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0102 | 0/0 | 4785 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0103 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0104 | 0/0 | 4788 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0105 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0106 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0107 | 0/0 | 4787 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0108 | 0/0 | 4787 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0109 | 0/0 | 4782 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0110 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0111 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0112 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0113 | 0/0 | 4782 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0114 | 0/0 | 4766 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0115 | 0/0 | 4772 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0116 | 0/0 | 4774 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0117 | 0/0 | 4789 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| t0118 | 0/0 | 4787 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0003 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0403 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0407 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0410 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0411 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0412 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| g0413 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| 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 | 0/0 | 2088 | 104 | 14 | 18 | 51 | 5 | 16 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0003 | 1/0 | 2088 | 50 | 14 | 10 | 19 | 2 | 4 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0010 | 0/0 | 2088 | 7 | 5 | 2 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0011 | 0/0 | 2088 | 5 | 2 | 1 | 0 | 1 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0019 | 0/0 | 2088 | 2 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0022 | 0/0 | 2088 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0026 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0029 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0030 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0034 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0047 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002 | 0/0 | 2088 | 82 | 0 | 9 | 68 | 0 | 5 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0004 | 0/0 | 2088 | 37 | 4 | 6 | 19 | 4 | 4 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0014 | 0/0 | 2088 | 4 | 0 | 0 | 4 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0015 | 0/0 | 2088 | 3 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0038 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0045 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0049 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005 | 0/1 | 2088 | 30 | 1 | 14 | 11 | 1 | 2 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0020 | 0/0 | 2088 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0025 | 0/0 | 2088 | 2 | 1 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0004c0008 | 0/0 | 2088 | 10 | 10 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0004c0028 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0005c0007 | 0/0 | 2088 | 10 | 0 | 7 | 0 | 2 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0006c0009 | 0/0 | 2088 | 7 | 6 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0006c0036 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0006c0044 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0006c0048 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0007c0012 | 0/0 | 2088 | 5 | 5 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0007c0016 | 0/0 | 2088 | 3 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0007c0037 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0007c0039 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0008c0006 | 0/0 | 2088 | 10 | 7 | 3 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0009c0013 | 0/0 | 2088 | 4 | 4 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0010c0017 | 0/0 | 2088 | 2 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0011c0021 | 0/0 | 2088 | 2 | 0 | 0 | 0 | 0 | 2 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0012c0023 | 0/0 | 2088 | 2 | 0 | 0 | 2 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0013c0024 | 0/0 | 2088 | 2 | 0 | 2 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0014c0018 | 0/0 | 2088 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0015c0031 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0016c0046 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0017c0033 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0018c0050 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0019c0051 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0020c0040 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0021c0027 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0022c0035 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0023c0043 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0024c0042 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0025c0041 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0026c0032 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0027c0052 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6857 | 26 | 0 | 4 | 20 | 1 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0004 | 0/0 | 6857 | 16 | 0 | 1 | 15 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0005 | 0/0 | 6861 | 14 | 0 | 7 | 3 | 0 | 4 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0006 | 0/0 | 6861 | 11 | 0 | 3 | 2 | 2 | 4 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0016 | 0/0 | 6858 | 2 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0017 | 0/0 | 6866 | 4 | 4 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0021 | 0/0 | 6861 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0028 | 0/0 | 6862 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0031 | 0/0 | 6856 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0032 | 0/0 | 6861 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0037 | 0/0 | 6861 | 2 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0038 | 0/0 | 6861 | 2 | 0 | 0 | 1 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0045 | 0/0 | 6857 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0048 | 0/0 | 6858 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0052 | 0/0 | 6852 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0054 | 0/0 | 6861 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0055 | 0/0 | 6872 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0056 | 0/0 | 6861 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0057 | 0/0 | 6861 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0058 | 0/0 | 6861 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0059 | 0/0 | 6866 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0060 | 0/0 | 6866 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0061 | 0/0 | 6871 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0062 | 0/0 | 6871 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0063 | 0/0 | 6876 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0071 | 0/0 | 6857 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0094 | 0/0 | 6890 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0097 | 0/0 | 6851 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0098 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0099 | 0/0 | 6861 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0100 | 0/0 | 6866 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0101 | 0/0 | 6866 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0001t0116 | 0/0 | 6861 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0003t0001 | 1/0 | 6857 | 28 | 3 | 6 | 16 | 0 | 2 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0003t0004 | 0/0 | 6857 | 4 | 1 | 2 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0003t0016 | 0/0 | 6858 | 2 | 0 | 1 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0003t0020 | 0/0 | 6892 | 3 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0003t0026 | 0/0 | 6852 | 3 | 2 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0003t0027 | 0/0 | 6867 | 3 | 2 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0003t0030 | 0/0 | 6892 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0003t0036 | 0/0 | 6890 | 2 | 0 | 0 | 0 | 1 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0003t0093 | 0/0 | 6857 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0003t0095 | 0/0 | 6857 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0003t0096 | 0/0 | 6857 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0010t0009 | 0/0 | 6863 | 6 | 4 | 2 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0010t0053 | 0/0 | 6863 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0011t0001 | 0/0 | 6857 | 5 | 2 | 1 | 0 | 1 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0019t0004 | 0/0 | 6857 | 2 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0022t0090 | 0/0 | 6892 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0022t0091 | 0/0 | 6867 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0026t0001 | 0/0 | 6857 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0029t0051 | 0/0 | 6874 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0030t0032 | 0/0 | 6861 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0034t0009 | 0/0 | 6863 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0001c0047t0001 | 0/0 | 6857 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0002 | 0/0 | 6874 | 32 | 0 | 4 | 24 | 0 | 4 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0003 | 0/0 | 6874 | 30 | 0 | 0 | 29 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0013 | 0/0 | 6875 | 4 | 0 | 0 | 4 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0015 | 0/0 | 6874 | 5 | 0 | 5 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0018 | 0/0 | 6874 | 3 | 0 | 0 | 3 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0029 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0039 | 0/0 | 6874 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0049 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0075 | 0/0 | 6874 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0076 | 0/0 | 6858 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0078 | 0/0 | 6876 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0104 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0002t0105 | 0/0 | 6874 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0004t0002 | 0/0 | 6874 | 11 | 2 | 1 | 8 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0004t0003 | 0/0 | 6874 | 14 | 2 | 4 | 4 | 2 | 2 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0004t0012 | 0/0 | 6874 | 4 | 0 | 0 | 4 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0004t0013 | 0/0 | 6875 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0004t0039 | 0/0 | 6874 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0004t0044 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0004t0072 | 0/0 | 6874 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0004t0077 | 0/0 | 6874 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0004t0106 | 0/0 | 6874 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0004t0107 | 0/0 | 6874 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0004t0108 | 0/0 | 6874 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0014t0002 | 0/0 | 6874 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0014t0003 | 0/0 | 6874 | 3 | 0 | 0 | 3 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0015t0002 | 0/0 | 6874 | 3 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0038t0118 | 0/0 | 6874 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0045t0029 | 0/0 | 6875 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0002c0049t0073 | 0/0 | 6874 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0008 | 0/0 | 6869 | 8 | 0 | 8 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0011 | 0/0 | 6853 | 7 | 0 | 0 | 7 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0025 | 0/1 | 6853 | 3 | 0 | 2 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0041 | 0/0 | 6853 | 2 | 0 | 2 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0042 | 0/0 | 6853 | 2 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0043 | 0/0 | 6853 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0087 | 0/0 | 6869 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0088 | 0/0 | 6852 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0109 | 0/0 | 6869 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0110 | 0/0 | 6833 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0112 | 0/0 | 6853 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0113 | 0/0 | 6869 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0005t0114 | 0/0 | 6853 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0020t0083 | 0/0 | 6854 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0020t0084 | 0/0 | 6838 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0025t0043 | 0/0 | 6853 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0003c0025t0085 | 0/0 | 6853 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0004c0008t0010 | 0/0 | 6862 | 7 | 7 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0004c0008t0064 | 0/0 | 6862 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0004c0008t0069 | 0/0 | 6866 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0004c0008t0070 | 0/0 | 6862 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0004c0028t0067 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0005c0007t0007 | 0/0 | 6859 | 8 | 0 | 5 | 0 | 2 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0005c0007t0089 | 0/0 | 6859 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0005c0007t0115 | 0/0 | 6859 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0006c0009t0014 | 0/0 | 6871 | 5 | 4 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0006c0009t0102 | 0/0 | 6872 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0006c0009t0117 | 0/0 | 6876 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0006c0036t0033 | 0/0 | 6872 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0006c0044t0033 | 0/0 | 6872 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0006c0048t0065 | 0/0 | 6872 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0007c0012t0019 | 0/0 | 6889 | 4 | 4 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0007c0012t0080 | 0/0 | 6874 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0007c0016t0035 | 0/0 | 6874 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0007c0016t0050 | 0/0 | 6875 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0007c0016t0079 | 0/0 | 6874 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0007c0037t0035 | 0/0 | 6874 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0007c0039t0092 | 0/0 | 6866 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0008c0006t0023 | 0/0 | 6838 | 3 | 2 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0008c0006t0024 | 0/0 | 6853 | 3 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0008c0006t0046 | 0/0 | 6854 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0008c0006t0082 | 0/0 | 6838 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0008c0006t0086 | 0/0 | 6853 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0008c0006t0111 | 0/0 | 6838 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0009c0013t0022 | 0/0 | 6862 | 3 | 3 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0009c0013t0068 | 0/0 | 6862 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0010c0017t0007 | 0/0 | 6859 | 2 | 0 | 1 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0011c0021t0040 | 0/0 | 6874 | 2 | 0 | 0 | 0 | 0 | 2 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0012c0023t0001 | 0/0 | 6857 | 2 | 0 | 0 | 2 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0013c0024t0001 | 0/0 | 6857 | 2 | 0 | 2 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0014c0018t0034 | 0/0 | 6867 | 2 | 2 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0015c0031t0103 | 0/0 | 6874 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0016c0046t0002 | 0/0 | 6874 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0017c0033t0012 | 0/0 | 6874 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0018c0050t0066 | 0/0 | 6872 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0019c0051t0081 | 0/0 | 6889 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0020c0040t0001 | 0/0 | 6857 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0021c0027t0047 | 0/0 | 6860 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0022c0035t0028 | 0/0 | 6862 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0023c0043t0018 | 0/0 | 6811 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0024c0042t0074 | 0/0 | 6874 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0025c0041t0002 | 0/0 | 6874 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0026c0032t0021 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| a0027c0052t0001 | 0/0 | 6857 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | copy fasta | chr7 | 2553979 | 2619728 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0410 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0411 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0001g0412 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0005g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0006g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0006g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0006g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0006g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0006g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0016g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0016g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0017g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0017g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0017g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0017g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0021g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0021g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0028g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0031g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0031g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0032g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0037g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0037g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0038g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0038g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0045g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0048g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0052g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0054g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0055g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0056g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0057g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0058g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0059g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0060g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0061g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0062g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0063g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0071g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0094g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0097g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0098g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0099g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0100g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0101g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0001t0116g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0001g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0016g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0016g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0020g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0020g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0020g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0026g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0026g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0026g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0027g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0027g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0027g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0030g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0030g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0036g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0036g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0093g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0095g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0003t0096g0407 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0010t0009g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0010t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0010t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0010t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0010t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0010t0009g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0010t0053g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0011t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0011t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0011t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0011t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0011t0001g0413 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0019t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0019t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0022t0090g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0022t0091g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0026t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0029t0051g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0030t0032g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0034t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0001c0047t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0003g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0013g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0013g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0013g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0013g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0015g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0015g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0015g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0015g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0015g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0018g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0018g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0018g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0029g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0039g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0049g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0075g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0076g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0078g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0104g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0002t0105g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0003g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0012g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0012g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0012g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0012g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0013g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0039g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0044g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0072g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0077g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0106g0403 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0107g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0004t0108g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0014t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0014t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0014t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0014t0003g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0015t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0015t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0015t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0038t0118g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0045t0029g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0002c0049t0073g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0008g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0008g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0008g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0008g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0008g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0008g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0008g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0008g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0011g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0011g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0011g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0011g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0011g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0011g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0025g0003 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0025g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0041g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0041g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0042g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0042g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0043g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0087g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0088g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0109g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0110g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0112g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0113g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0005t0114g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0020t0083g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0020t0084g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0025t0043g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0003c0025t0085g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0004c0008t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0004c0008t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0004c0008t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0004c0008t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0004c0008t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0004c0008t0010g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0004c0008t0010g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0004c0008t0064g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0004c0008t0069g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0004c0008t0070g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0004c0028t0067g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0005c0007t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0005c0007t0007g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0005c0007t0007g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0005c0007t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0005c0007t0007g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0005c0007t0007g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0005c0007t0007g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0005c0007t0007g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0005c0007t0089g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0005c0007t0115g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0006c0009t0014g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0006c0009t0014g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0006c0009t0014g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0006c0009t0014g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0006c0009t0014g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0006c0009t0102g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0006c0009t0117g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0006c0036t0033g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0006c0044t0033g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0006c0048t0065g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0007c0012t0019g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0007c0012t0019g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0007c0012t0019g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0007c0012t0019g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0007c0012t0080g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0007c0016t0035g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0007c0016t0050g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0007c0016t0079g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0007c0037t0035g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0007c0039t0092g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0008c0006t0023g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0008c0006t0023g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0008c0006t0023g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0008c0006t0024g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0008c0006t0024g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0008c0006t0024g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0008c0006t0046g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0008c0006t0082g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0008c0006t0086g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0008c0006t0111g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0009c0013t0022g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0009c0013t0022g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0009c0013t0022g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0009c0013t0068g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0010c0017t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0010c0017t0007g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0011c0021t0040g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0011c0021t0040g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0012c0023t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0012c0023t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0013c0024t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0013c0024t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0014c0018t0034g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0014c0018t0034g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0015c0031t0103g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0016c0046t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0017c0033t0012g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0018c0050t0066g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0019c0051t0081g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0020c0040t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0021c0027t0047g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0022c0035t0028g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0023c0043t0018g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0024c0042t0074g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0025c0041t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0026c0032t0021g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| a0027c0052t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0036 | g0245 | EUR | GBR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00099 | hp2 | a0003 | c0005 | t0110 | g0258 | EUR | GBR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00140 | hp1 | a0001 | c0011 | t0001 | g0342 | EUR | GBR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00140 | hp2 | a0001 | c0001 | t0032 | g0079 | EUR | GBR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00280 | hp1 | a0001 | c0030 | t0032 | g0068 | EUR | FIN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00280 | hp2 | a0005 | c0007 | t0007 | g0276 | EUR | FIN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0329 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00408 | hp2 | a0002 | c0004 | t0012 | g0357 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0323 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0301 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00438 | hp1 | a0001 | c0001 | t0058 | g0307 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00438 | hp2 | a0001 | c0001 | t0045 | g0396 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00544 | hp1 | a0002 | c0002 | t0003 | g0319 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00544 | hp2 | a0002 | c0002 | t0039 | g0209 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00597 | hp1 | a0002 | c0004 | t0003 | g0213 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00609 | hp1 | a0002 | c0038 | t0118 | g0025 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00609 | hp2 | a0002 | c0002 | t0003 | g0240 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00621 | hp1 | a0003 | c0005 | t0043 | g0341 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | CHS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00639 | hp1 | a0002 | c0004 | t0002 | g0163 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00639 | hp2 | a0006 | c0048 | t0065 | g0165 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00642 | hp1 | a0003 | c0005 | t0041 | g0330 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00642 | hp2 | a0003 | c0005 | t0041 | g0337 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00733 | hp1 | a0005 | c0007 | t0007 | g0275 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00733 | hp2 | a0010 | c0017 | t0007 | g0002 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0265 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00735 | hp2 | a0001 | c0003 | t0004 | g0098 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00738 | hp1 | a0002 | c0004 | t0077 | g0104 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00738 | hp2 | a0001 | c0003 | t0004 | g0174 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0180 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG00741 | hp2 | a0001 | c0001 | t0054 | g0273 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01069 | hp1 | a0003 | c0005 | t0025 | g0167 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0279 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01070 | hp1 | a0005 | c0007 | t0089 | g0077 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0217 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0216 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01071 | hp2 | a0003 | c0005 | t0025 | g0003 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0166 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01074 | hp2 | a0001 | c0019 | t0004 | g0093 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01081 | hp1 | a0006 | c0009 | t0014 | g0267 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01099 | hp1 | a0001 | c0011 | t0001 | g0314 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01099 | hp2 | a0003 | c0005 | t0008 | g0192 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01106 | hp1 | a0002 | c0004 | t0003 | g0364 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01106 | hp2 | a0002 | c0045 | t0029 | g0080 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0282 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01109 | hp2 | a0001 | c0029 | t0051 | g0171 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0178 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01167 | hp2 | a0008 | c0006 | t0023 | g0146 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0281 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0175 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01175 | hp1 | a0001 | c0003 | t0016 | g0219 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01175 | hp2 | a0013 | c0024 | t0001 | g0201 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01192 | hp1 | a0008 | c0006 | t0046 | g0111 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01192 | hp2 | a0001 | c0010 | t0009 | g0157 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01243 | hp1 | a0001 | c0010 | t0009 | g0005 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01243 | hp2 | a0008 | c0006 | t0082 | g0108 | AMR | PUR | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01255 | hp1 | a0003 | c0005 | t0008 | g0193 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01255 | hp2 | a0002 | c0004 | t0003 | g0257 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01256 | hp1 | a0005 | c0007 | t0115 | g0277 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01256 | hp2 | a0002 | c0002 | t0015 | g0359 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01257 | hp1 | a0001 | c0001 | t0037 | g0376 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01258 | hp1 | a0002 | c0002 | t0015 | g0321 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0041 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01261 | hp2 | a0003 | c0005 | t0008 | g0187 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0102 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01346 | hp2 | a0005 | c0007 | t0007 | g0262 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0313 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01433 | hp2 | a0003 | c0005 | t0008 | g0177 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0390 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01496 | hp2 | a0001 | c0003 | t0027 | g0325 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01515 | hp1 | a0002 | c0004 | t0039 | g0356 | EUR | IBS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0233 | EUR | IBS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01516 | hp1 | a0002 | c0004 | t0003 | g0223 | EUR | IBS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01516 | hp2 | a0005 | c0007 | t0007 | g0067 | EUR | IBS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0250 | EUR | IBS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01517 | hp2 | a0002 | c0004 | t0003 | g0238 | EUR | IBS | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01884 | hp1 | a0004 | c0008 | t0010 | g0016 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01884 | hp2 | a0001 | c0001 | t0098 | g0371 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01891 | hp1 | a0001 | c0047 | t0001 | g0308 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01891 | hp2 | a0001 | c0003 | t0030 | g0048 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01934 | hp1 | a0005 | c0007 | t0007 | g0002 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01934 | hp2 | a0003 | c0005 | t0114 | g0251 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01943 | hp2 | a0003 | c0005 | t0008 | g0182 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01952 | hp1 | a0003 | c0005 | t0008 | g0191 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01952 | hp2 | a0001 | c0001 | t0016 | g0204 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01975 | hp1 | a0003 | c0005 | t0008 | g0189 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0069 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01978 | hp1 | a0025 | c0041 | t0002 | g0123 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0103 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01981 | hp1 | a0003 | c0005 | t0042 | g0369 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0156 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01993 | hp1 | a0003 | c0005 | t0008 | g0190 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01993 | hp2 | a0002 | c0002 | t0015 | g0348 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0070 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02015 | hp1 | a0001 | c0001 | t0038 | g0328 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02027 | hp1 | a0001 | c0001 | t0059 | g0393 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0338 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02055 | hp1 | a0002 | c0004 | t0002 | g0109 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02055 | hp2 | a0002 | c0015 | t0002 | g0076 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0408 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0346 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02074 | hp2 | a0002 | c0004 | t0012 | g0383 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02080 | hp1 | a0002 | c0002 | t0049 | g0399 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02080 | hp2 | a0002 | c0002 | t0003 | g0362 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02083 | hp1 | a0001 | c0001 | t0094 | g0409 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02083 | hp2 | a0002 | c0002 | t0003 | g0298 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02132 | hp2 | a0001 | c0001 | t0071 | g0032 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02135 | hp1 | a0002 | c0002 | t0003 | g0302 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02145 | hp1 | a0006 | c0036 | t0033 | g0172 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02145 | hp2 | a0004 | c0008 | t0010 | g0052 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02148 | hp1 | a0002 | c0002 | t0015 | g0382 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02148 | hp2 | a0016 | c0046 | t0002 | g0056 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02165 | hp1 | a0002 | c0002 | t0003 | g0361 | EAS | CDX | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0332 | EAS | CDX | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02257 | hp1 | a0009 | c0013 | t0022 | g0154 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02257 | hp2 | a0002 | c0004 | t0003 | g0269 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02258 | hp1 | a0006 | c0009 | t0102 | g0214 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02258 | hp2 | a0001 | c0003 | t0030 | g0155 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02273 | hp2 | a0002 | c0004 | t0003 | g0244 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02280 | hp1 | a0004 | c0008 | t0010 | g0018 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02280 | hp2 | a0001 | c0001 | t0017 | g0144 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02293 | hp1 | a0002 | c0002 | t0015 | g0316 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02293 | hp2 | a0005 | c0007 | t0007 | g0106 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02300 | hp1 | a0002 | c0004 | t0003 | g0290 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02300 | hp2 | a0005 | c0007 | t0007 | g0101 | AMR | PEL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02451 | hp1 | a0001 | c0022 | t0091 | g0081 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02451 | hp2 | a0001 | c0001 | t0031 | g0116 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02523 | hp1 | a0002 | c0002 | t0029 | g0031 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02523 | hp2 | a0002 | c0004 | t0003 | g0375 | EAS | KHV | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02572 | hp1 | a0008 | c0006 | t0086 | g0125 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02572 | hp2 | a0008 | c0006 | t0111 | g0405 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02602 | hp1 | a0021 | c0027 | t0047 | g0243 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02602 | hp2 | a0001 | c0001 | t0016 | g0264 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02615 | hp1 | a0008 | c0006 | t0023 | g0004 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02615 | hp2 | a0001 | c0011 | t0001 | g0381 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02622 | hp1 | a0006 | c0009 | t0014 | g0280 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02622 | hp2 | a0002 | c0004 | t0003 | g0406 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02647 | hp1 | a0006 | c0009 | t0014 | g0366 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02647 | hp2 | a0004 | c0008 | t0010 | g0024 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02698 | hp1 | a0005 | c0007 | t0007 | g0278 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0073 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02717 | hp1 | a0007 | c0012 | t0019 | g0139 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02717 | hp2 | a0001 | c0001 | t0017 | g0140 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0202 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02723 | hp2 | a0001 | c0010 | t0009 | g0121 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0088 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02735 | hp2 | a0002 | c0004 | t0108 | g0259 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02738 | hp1 | a0003 | c0005 | t0042 | g0378 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02738 | hp2 | a0001 | c0019 | t0004 | g0105 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02809 | hp1 | a0003 | c0020 | t0083 | g0159 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02809 | hp2 | a0007 | c0012 | t0019 | g0168 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02818 | hp1 | a0001 | c0022 | t0090 | g0082 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02818 | hp2 | a0006 | c0009 | t0014 | g0387 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02886 | hp1 | a0001 | c0003 | t0004 | g0099 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02886 | hp2 | a0007 | c0012 | t0019 | g0138 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02895 | hp1 | a0007 | c0012 | t0019 | g0120 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02895 | hp2 | a0001 | c0003 | t0020 | g0118 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02896 | hp1 | a0014 | c0018 | t0034 | g0115 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02896 | hp2 | a0004 | c0008 | t0010 | g0019 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02897 | hp1 | a0014 | c0018 | t0034 | g0114 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02897 | hp2 | a0001 | c0003 | t0020 | g0119 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02922 | hp1 | a0004 | c0028 | t0067 | g0020 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02922 | hp2 | a0001 | c0003 | t0027 | g0271 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02965 | hp1 | a0019 | c0051 | t0081 | g0128 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02965 | hp2 | a0003 | c0020 | t0084 | g0160 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02970 | hp1 | a0004 | c0008 | t0070 | g0198 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02970 | hp2 | a0007 | c0016 | t0079 | g0145 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02976 | hp1 | a0018 | c0050 | t0066 | g0117 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02976 | hp2 | a0008 | c0006 | t0023 | g0107 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0260 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03017 | hp2 | a0003 | c0005 | t0113 | g0283 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03041 | hp1 | a0001 | c0010 | t0009 | g0149 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03041 | hp2 | a0003 | c0025 | t0085 | g0110 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03098 | hp1 | a0007 | c0016 | t0050 | g0266 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03098 | hp2 | a0002 | c0015 | t0002 | g0097 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03130 | hp1 | a0001 | c0001 | t0021 | g0129 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0336 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03139 | hp1 | a0001 | c0001 | t0062 | g0113 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03139 | hp2 | a0008 | c0006 | t0024 | g0151 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03195 | hp1 | a0007 | c0039 | t0092 | g0013 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03195 | hp2 | a0008 | c0006 | t0024 | g0127 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03209 | hp1 | a0001 | c0010 | t0009 | g0124 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03209 | hp2 | a0004 | c0008 | t0064 | g0197 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03225 | hp1 | a0001 | c0001 | t0101 | g0235 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03225 | hp2 | a0008 | c0006 | t0024 | g0112 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03239 | hp1 | a0001 | c0001 | t0100 | g0199 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03239 | hp2 | a0001 | c0001 | t0056 | g0131 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03453 | hp1 | a0001 | c0001 | t0017 | g0083 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03453 | hp2 | a0009 | c0013 | t0022 | g0084 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0287 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03486 | hp2 | a0001 | c0001 | t0021 | g0130 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03492 | hp1 | a0002 | c0004 | t0003 | g0295 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0094 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03516 | hp1 | a0001 | c0001 | t0017 | g0152 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03516 | hp2 | a0001 | c0034 | t0009 | g0169 | AFR | ESN | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03540 | hp1 | a0007 | c0012 | t0080 | g0135 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03540 | hp2 | a0004 | c0008 | t0010 | g0015 | AFR | GWD | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03579 | hp1 | a0009 | c0013 | t0068 | g0100 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03579 | hp2 | a0001 | c0001 | t0063 | g0150 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03654 | hp1 | a0001 | c0001 | t0037 | g0372 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0057 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03669 | hp1 | a0001 | c0011 | t0001 | g0413 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0255 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0010 | SAS | STU | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0274 | SAS | STU | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03704 | hp1 | a0001 | c0003 | t0095 | g0345 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03704 | hp2 | a0001 | c0003 | t0036 | g0247 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03710 | hp1 | a0002 | c0004 | t0003 | g0358 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03710 | hp2 | a0001 | c0001 | t0097 | g0286 | SAS | PJL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03831 | hp2 | a0010 | c0017 | t0007 | g0092 | SAS | BEB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03834 | hp1 | a0001 | c0001 | t0060 | g0042 | SAS | BEB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03834 | hp2 | a0011 | c0021 | t0040 | g0374 | SAS | BEB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0095 | SAS | STU | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0236 | SAS | STU | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | BEB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG04184 | hp2 | a0001 | c0026 | t0001 | g0380 | SAS | BEB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG04199 | hp1 | a0027 | c0052 | t0001 | g0344 | SAS | STU | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG04199 | hp2 | a0002 | c0004 | t0013 | g0256 | SAS | STU | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0239 | SAS | STU | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG04204 | hp2 | a0001 | c0001 | t0116 | g0263 | SAS | STU | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG04228 | hp1 | a0002 | c0002 | t0003 | g0340 | SAS | STU | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG04228 | hp2 | a0011 | c0021 | t0040 | g0370 | SAS | STU | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18522 | hp1 | a0004 | c0008 | t0069 | g0017 | AFR | YRI | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18522 | hp2 | a0002 | c0015 | t0002 | g0075 | AFR | YRI | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18612 | hp1 | a0002 | c0002 | t0105 | g0317 | EAS | CHB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0411 | EAS | CHB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18747 | hp1 | a0002 | c0002 | t0003 | g0355 | EAS | CHB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | CHB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18906 | hp1 | a0001 | c0010 | t0053 | g0137 | AFR | YRI | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18906 | hp2 | a0006 | c0044 | t0033 | g0085 | AFR | YRI | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18939 | hp2 | a0003 | c0025 | t0043 | g0339 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18942 | hp1 | a0002 | c0014 | t0002 | g0046 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18942 | hp2 | a0002 | c0002 | t0003 | g0232 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18944 | hp1 | a0002 | c0002 | t0003 | g0293 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18945 | hp1 | a0002 | c0002 | t0003 | g0350 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0410 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18946 | hp2 | a0002 | c0002 | t0003 | g0398 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18947 | hp2 | a0001 | c0001 | t0099 | g0305 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0333 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18948 | hp2 | a0002 | c0004 | t0002 | g0007 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18951 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18952 | hp1 | a0003 | c0005 | t0087 | g0185 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18953 | hp1 | a0002 | c0004 | t0044 | g0304 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18953 | hp2 | a0002 | c0002 | t0013 | g0220 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18956 | hp1 | a0001 | c0001 | t0061 | g0176 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18956 | hp2 | a0002 | c0002 | t0003 | g0404 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18957 | hp2 | a0002 | c0002 | t0003 | g0353 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18960 | hp2 | a0002 | c0002 | t0003 | g0360 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18961 | hp1 | a0001 | c0003 | t0016 | g0311 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0312 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18964 | hp1 | a0002 | c0004 | t0002 | g0008 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18964 | hp2 | a0002 | c0002 | t0003 | g0392 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0368 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18969 | hp1 | a0022 | c0035 | t0028 | g0326 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0389 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18970 | hp1 | a0002 | c0002 | t0003 | g0252 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18970 | hp2 | a0003 | c0005 | t0109 | g0254 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18971 | hp2 | a0002 | c0002 | t0003 | g0402 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18977 | hp1 | a0003 | c0005 | t0011 | g0195 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18977 | hp2 | a0002 | c0002 | t0003 | g0401 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18979 | hp1 | a0002 | c0004 | t0002 | g0011 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0377 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0324 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18983 | hp2 | a0002 | c0004 | t0002 | g0148 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18984 | hp1 | a0001 | c0003 | t0004 | g0071 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18984 | hp2 | a0015 | c0031 | t0103 | g0296 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18988 | hp2 | a0024 | c0042 | t0074 | g0059 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18990 | hp1 | a0002 | c0002 | t0003 | g0363 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18990 | hp2 | a0002 | c0004 | t0002 | g0012 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18991 | hp1 | a0003 | c0005 | t0011 | g0181 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18991 | hp2 | a0002 | c0002 | t0013 | g0385 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18993 | hp1 | a0002 | c0002 | t0003 | g0253 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18994 | hp1 | a0002 | c0002 | t0003 | g0384 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0379 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18995 | hp2 | a0002 | c0002 | t0018 | g0179 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18999 | hp1 | a0003 | c0005 | t0011 | g0188 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA18999 | hp2 | a0002 | c0002 | t0003 | g0352 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19000 | hp1 | a0002 | c0002 | t0003 | g0318 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19000 | hp2 | a0002 | c0002 | t0076 | g0065 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19002 | hp1 | a0002 | c0014 | t0003 | g0248 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19002 | hp2 | a0002 | c0002 | t0018 | g0136 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19003 | hp1 | a0002 | c0004 | t0012 | g0294 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19003 | hp2 | a0003 | c0005 | t0088 | g0164 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0349 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19004 | hp2 | a0001 | c0001 | t0057 | g0327 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19007 | hp1 | a0002 | c0002 | t0003 | g0291 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0335 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19012 | hp1 | a0002 | c0004 | t0072 | g0162 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19030 | hp1 | a0001 | c0001 | t0031 | g0142 | AFR | LWK | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19030 | hp2 | a0002 | c0049 | t0073 | g0054 | AFR | LWK | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19043 | hp1 | a0026 | c0032 | t0021 | g0023 | AFR | LWK | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19043 | hp2 | a0001 | c0001 | t0052 | g0060 | AFR | LWK | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19054 | hp1 | a0012 | c0023 | t0001 | g0288 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0412 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0334 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19057 | hp2 | a0002 | c0004 | t0003 | g0221 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19060 | hp1 | a0003 | c0005 | t0011 | g0194 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19060 | hp2 | a0020 | c0040 | t0001 | g0310 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19064 | hp1 | a0002 | c0002 | t0003 | g0354 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19065 | hp1 | a0012 | c0023 | t0001 | g0297 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19065 | hp2 | a0002 | c0014 | t0003 | g0231 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19067 | hp1 | a0003 | c0005 | t0011 | g0186 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19068 | hp2 | a0002 | c0004 | t0003 | g0261 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19070 | hp1 | a0001 | c0003 | t0096 | g0407 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19070 | hp2 | a0002 | c0002 | t0018 | g0132 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19074 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19076 | hp1 | a0003 | c0005 | t0011 | g0050 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19076 | hp2 | a0002 | c0002 | t0078 | g0062 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19077 | hp1 | a0002 | c0002 | t0013 | g0400 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19077 | hp2 | a0002 | c0002 | t0013 | g0351 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19078 | hp1 | a0023 | c0043 | t0018 | g0147 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19078 | hp2 | a0001 | c0001 | t0048 | g0242 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19079 | hp2 | a0001 | c0001 | t0028 | g0306 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0270 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19080 | hp2 | a0003 | c0005 | t0011 | g0196 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19081 | hp1 | a0002 | c0004 | t0002 | g0009 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0309 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19083 | hp2 | a0001 | c0001 | t0006 | g0391 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19084 | hp1 | a0017 | c0033 | t0012 | g0320 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19084 | hp2 | a0001 | c0003 | t0001 | g0331 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19085 | hp1 | a0002 | c0002 | t0104 | g0292 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19086 | hp1 | a0002 | c0004 | t0012 | g0300 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19087 | hp1 | a0002 | c0002 | t0003 | g0322 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19087 | hp2 | a0002 | c0002 | t0075 | g0089 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19088 | hp1 | a0002 | c0004 | t0106 | g0403 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0397 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19091 | hp1 | a0002 | c0014 | t0003 | g0395 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19091 | hp2 | a0002 | c0002 | t0003 | g0394 | EAS | JPT | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19240 | hp1 | a0006 | c0009 | t0014 | g0303 | AFR | YRI | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA19240 | hp2 | a0009 | c0013 | t0022 | g0051 | AFR | YRI | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA20129 | hp1 | a0004 | c0008 | t0010 | g0022 | AFR | ASW | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA20129 | hp2 | a0001 | c0003 | t0027 | g0272 | AFR | ASW | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0284 | EUR | TSI | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA20752 | hp2 | a0002 | c0004 | t0107 | g0289 | EUR | TSI | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA20805 | hp1 | a0001 | c0001 | t0038 | g0367 | EUR | TSI | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA20805 | hp2 | a0001 | c0003 | t0026 | g0234 | EUR | TSI | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0388 | SAS | GIH | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0226 | SAS | GIH | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0285 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG01123 | hp2 | a0013 | c0024 | t0001 | g0203 | AMR | CLM | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02109 | hp1 | a0001 | c0001 | t0055 | g0170 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02109 | hp2 | a0007 | c0016 | t0035 | g0143 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02486 | hp1 | a0001 | c0010 | t0009 | g0122 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG02486 | hp2 | a0003 | c0005 | t0112 | g0373 | AFR | ACB | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03471 | hp1 | a0007 | c0037 | t0035 | g0014 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG03471 | hp2 | a0001 | c0003 | t0020 | g0021 | AFR | MSL | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG06807 | hp1 | a0001 | c0003 | t0026 | g0386 | AFR | USA | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| HG06807 | hp2 | a0001 | c0011 | t0001 | g0315 | AFR | USA | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA20300 | hp1 | a0002 | c0004 | t0002 | g0161 | AFR | USA | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA20300 | hp2 | a0006 | c0009 | t0117 | g0091 | AFR | USA | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA21309 | hp1 | a0001 | c0003 | t0093 | g0249 | AFR | LWK | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| NA21309 | hp2 | a0001 | c0003 | t0026 | g0365 | AFR | LWK | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0005 | t0025 | g0003 | REF | REF | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0200 | REF | REF | IQCE_chr7_2553979_2619728 | IQCE | chr7 | 2553979 | 2619728 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2567128
|
C | G | 1 | a0027 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.49C>G | p.Leu17Val | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/22 | 252/6857 | 49/2088 | 17/695 | chr7 | 2567128 | ||
| chr7:2571607
|
G | A | 1 | a0010 | 2 | HG00733.hp2 HG03831.hp2 |
missense_variant | MODERATE | c.212G>A | p.Arg71Gln | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 4/22 | 415/6857 | 212/2088 | 71/695 | chr7 | 2571607 | ||
| chr7:2572233
|
C | A | 2 | a0008a0014 | 12 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(9): Show |
missense_variant | MODERATE | c.301C>A | p.His101Asn | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/22 | 504/6857 | 301/2088 | 101/695 | chr7 | 2572233 | ||
| chr7:2586231
|
G | C | 1 | a0015 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.848G>C | p.Gly283Ala | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/22 | 1051/6857 | 848/2088 | 283/695 | chr7 | 2586231 | ||
| chr7:2586233
|
G | C | 1 | a0015 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.850G>C | p.Ala284Pro | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/22 | 1053/6857 | 850/2088 | 284/695 | chr7 | 2586233 | ||
| chr7:2586332
|
C | T | 1 | a0004 | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
missense_variant | MODERATE | c.949C>T | p.Arg317Cys | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/22 | 1152/6857 | 949/2088 | 317/695 | chr7 | 2586332 | ||
| chr7:2586368
|
C | G | 1 | a0011 | 2 | HG03834.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.985C>G | p.Gln329Glu | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/22 | 1188/6857 | 985/2088 | 329/695 | chr7 | 2586368 | ||
| chr7:2586369
|
A | C | 1 | a0016 | 1 | HG02148.hp2 | missense_variant&splice_region_variant | MODERATE | c.986A>C | p.Gln329Pro | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/22 | 1189/6857 | 986/2088 | 329/695 | chr7 | 2586369 | ||
| chr7:2587855
|
G | A | 1 | a0012 | 2 | NA19054.hp1 NA19065.hp1 |
missense_variant | MODERATE | c.1022G>A | p.Arg341Lys | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/22 | 1225/6857 | 1022/2088 | 341/695 | chr7 | 2587855 | ||
| chr7:2589973
|
T | C | 1 | a0026 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1111T>C | p.Cys371Arg | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/22 | 1314/6857 | 1111/2088 | 371/695 | chr7 | 2589973 | ||
| chr7:2590010
|
G | A | 1 | a0017 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.1148G>A | p.Arg383Gln | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/22 | 1351/6857 | 1148/2088 | 383/695 | chr7 | 2590010 | ||
| chr7:2590037
|
G | A | 1 | a0018 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1175G>A | p.Arg392His | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/22 | 1378/6857 | 1175/2088 | 392/695 | chr7 | 2590037 | ||
| chr7:2598555
|
C | T | 1 | a0004 | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
missense_variant | MODERATE | c.1531C>T | p.Arg511Cys | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/22 | 1734/6857 | 1531/2088 | 511/695 | chr7 | 2598555 | ||
| chr7:2604885
|
C | T | 13 | a0002a0003a0006others(10): Show | 202 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(199): Show |
missense_variant | MODERATE | c.1637C>T | p.Ala546Val | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/22 | 1840/6857 | 1637/2088 | 546/695 | chr7 | 2604885 | ||
| chr7:2605877
|
GCTCTCCT others(56): Show |
G | 1 | a0023 | 1 | NA19078.hp1 | disruptive_inframe_deletion&splice_region_variant | MODERATE | c.1746_1808delCTCTCC others(57): Show |
p.Ser582_Glu603delin others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/22 | 1949/6857 | 1746/2088 | 582/695 | chr7 | 2605877 | ||
| chr7:2605888
|
C | T | 1 | a0013 | 2 | HG01123.hp2 HG01175.hp2 |
missense_variant | MODERATE | c.1756C>T | p.Pro586Ser | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/22 | 1959/6857 | 1756/2088 | 586/695 | chr7 | 2605888 | ||
| chr7:2605892
|
G | A | 6 | a0002a0011a0016others(3): Show | 135 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(132): Show |
missense_variant | MODERATE | c.1760G>A | p.Arg587His | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/22 | 1963/6857 | 1760/2088 | 587/695 | chr7 | 2605892 | ||
| chr7:2605918
|
A | G | 12 | a0002a0003a0006others(9): Show | 201 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(198): Show |
missense_variant | MODERATE | c.1786A>G | p.Thr596Ala | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/22 | 1989/6857 | 1786/2088 | 596/695 | chr7 | 2605918 | ||
| chr7:2605924
|
A | C | 1 | a0024 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.1792A>C | p.Ser598Arg | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/22 | 1995/6857 | 1792/2088 | 598/695 | chr7 | 2605924 | ||
| chr7:2605951
|
A | G | 1 | a0022 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.1819A>G | p.Ile607Val | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/22 | 2022/6857 | 1819/2088 | 607/695 | chr7 | 2605951 | ||
| chr7:2607162
|
G | A | 2 | a0003a0008 | 44 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
missense_variant | MODERATE | c.1904G>A | p.Arg635Lys | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/22 | 2107/6857 | 1904/2088 | 635/695 | chr7 | 2607162 | ||
| chr7:2607171
|
C | G | 1 | a0009 | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.1913C>G | p.Ser638Trp | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/22 | 2116/6857 | 1913/2088 | 638/695 | chr7 | 2607171 | ||
| chr7:2607203
|
C | G | 1 | a0020 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.1945C>G | p.Pro649Ala | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/22 | 2148/6857 | 1945/2088 | 649/695 | chr7 | 2607203 | ||
| chr7:2610070
|
T | G | 15 | a0002a0003a0005others(12): Show | 205 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(202): Show |
missense_variant | MODERATE | c.1996T>G | p.Leu666Val | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2199/6857 | 1996/2088 | 666/695 | chr7 | 2610070 | ||
| chr7:2610131
|
C | T | 1 | a0021 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.2057C>T | p.Pro686Leu | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2260/6857 | 2057/2088 | 686/695 | chr7 | 2610131 | ||
| chr7:2610143
|
C | T | 4 | a0005a0010a0021others(1): Show | 14 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(11): Show |
missense_variant | MODERATE | c.2069C>T | p.Thr690Met | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2272/6857 | 2069/2088 | 690/695 | chr7 | 2610143 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2571548
|
G | A | 1 | a0002c0015 | 3 | HG02055.hp2 HG03098.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.153G>A | p.Pro51Pro | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 4/22 | 356/6857 | 153/2088 | 51/695 | chr7 | 2571548 | ||
| chr7:2572202
|
C | A | 1 | a0001c0026 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.270C>A | p.Thr90Thr | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/22 | 473/6857 | 270/2088 | 90/695 | chr7 | 2572202 | ||
| chr7:2572244
|
T | C | 27 | a0001c0001a0001c0019a0001c0026others(24): Show | 236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
synonymous_variant | LOW | c.312T>C | p.Thr104Thr | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/22 | 515/6857 | 312/2088 | 104/695 | chr7 | 2572244 | ||
| chr7:2572256
|
C | T | 3 | a0007c0012a0018c0050a0019c0051 | 7 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(4): Show |
synonymous_variant | LOW | c.324C>T | p.Gly108Gly | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/22 | 527/6857 | 324/2088 | 108/695 | chr7 | 2572256 | ||
| chr7:2572274
|
G | C | 2 | a0001c0022a0007c0039 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.342G>C | p.Leu114Leu | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/22 | 545/6857 | 342/2088 | 114/695 | chr7 | 2572274 | ||
| chr7:2573428
|
T | C | 8 | a0001c0019a0001c0029a0004c0008others(5): Show | 28 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(25): Show |
synonymous_variant | LOW | c.405T>C | p.Pro135Pro | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/22 | 608/6857 | 405/2088 | 135/695 | chr7 | 2573428 | ||
| chr7:2582639
|
C | T | 1 | a0002c0038 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.690C>T | p.Asp230Asp | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/22 | 893/6857 | 690/2088 | 230/695 | chr7 | 2582639 | ||
| chr7:2584247
|
C | G | 4 | a0001c0029a0002c0049a0007c0016others(1): Show | 6 | HG01109.hp2 HG02109.hp2 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.786C>G | p.Leu262Leu | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/22 | 989/6857 | 786/2088 | 262/695 | chr7 | 2584247 | ||
| chr7:2584277
|
C | T | 2 | a0001c0047a0006c0048 | 2 | HG00639.hp2 HG01891.hp1 |
synonymous_variant | LOW | c.816C>T | p.Thr272Thr | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/22 | 1019/6857 | 816/2088 | 272/695 | chr7 | 2584277 | ||
| chr7:2586214
|
G | A | 1 | a0001c0030 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.831G>A | p.Leu277Leu | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/22 | 1034/6857 | 831/2088 | 277/695 | chr7 | 2586214 | ||
| chr7:2586232
|
C | G | 1 | a0015c0031 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.849C>G | p.Gly283Gly | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/22 | 1052/6857 | 849/2088 | 283/695 | chr7 | 2586232 | ||
| chr7:2586262
|
C | T | 1 | a0007c0012 | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.879C>T | p.Ala293Ala | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/22 | 1082/6857 | 879/2088 | 293/695 | chr7 | 2586262 | ||
| chr7:2590026
|
G | A | 1 | a0007c0012 | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.1164G>A | p.Lys388Lys | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/22 | 1367/6857 | 1164/2088 | 388/695 | chr7 | 2590026 | ||
| chr7:2590060
|
C | T | 1 | a0002c0045 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.1198C>T | p.Leu400Leu | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/22 | 1401/6857 | 1198/2088 | 400/695 | chr7 | 2590060 | ||
| chr7:2590095
|
G | A | 1 | a0001c0011 | 5 | HG00140.hp1 HG01099.hp1 HG02615.hp2 others(2): Show |
synonymous_variant | LOW | c.1233G>A | p.Leu411Leu | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/22 | 1436/6857 | 1233/2088 | 411/695 | chr7 | 2590095 | ||
| chr7:2594901
|
A | G | 3 | a0001c0029a0004c0028a0007c0012 | 7 | HG01109.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
synonymous_variant | LOW | c.1365A>G | p.Thr455Thr | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/22 | 1568/6857 | 1365/2088 | 455/695 | chr7 | 2594901 | ||
| chr7:2604973
|
G | T | 5 | a0003c0005a0003c0025a0006c0036others(2): Show | 44 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
synonymous_variant | LOW | c.1725G>T | p.Val575Val | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/22 | 1928/6857 | 1725/2088 | 575/695 | chr7 | 2604973 | ||
| chr7:2607193
|
C | T | 1 | a0002c0014 | 4 | NA18942.hp1 NA19002.hp1 NA19065.hp2 others(1): Show |
synonymous_variant | LOW | c.1935C>T | p.Asp645Asp | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/22 | 2138/6857 | 1935/2088 | 645/695 | chr7 | 2607193 | ||
| chr7:2610051
|
T | C | 2 | a0001c0010a0001c0034 | 8 | HG01192.hp2 HG01243.hp1 HG02486.hp1 others(5): Show |
synonymous_variant | LOW | c.1977T>C | p.Ser659Ser | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2180/6857 | 1977/2088 | 659/695 | chr7 | 2610051 | ||
| chr7:2610111
|
C | T | 1 | a0009c0013 | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.2037C>T | p.Ser679Ser | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2240/6857 | 2037/2088 | 679/695 | chr7 | 2610111 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2558984
|
C | T | 1 | a0002c0038t0118 | 1 | HG00609.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-198C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/22 | chr7 | 2558984 | ||||||
| chr7:2559024
|
G | A | 4 | a0001c0001t0045a0002c0004t0012a0002c0004t0044others(1): Show | 7 | HG00408.hp2 HG00438.hp2 HG02074.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-158G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/22 | 158 | chr7 | 2559024 | |||||
| chr7:2559059
|
C | CG | 14 | a0001c0001t0016a0001c0001t0028a0001c0001t0048others(11): Show | 19 | HG01106.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-119dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/22 | 118 | INFO_REALIGN_3_PRIME | chr7 | 2559059 | ||||
| chr7:2559071
|
C | G | 1 | a0006c0009t0117 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-111C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/22 | 111 | chr7 | 2559071 | |||||
| chr7:2559090
|
C | G | 1 | a0002c0002t0015 | 5 | HG01256.hp2 HG01258.hp1 HG01993.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-92C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/22 | 92 | chr7 | 2559090 | |||||
| chr7:2559107
|
A | C | 1 | a0001c0001t0116 | 1 | HG04204.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/22 | 75 | chr7 | 2559107 | |||||
| chr7:2559123
|
T | C | 87 | a0001c0001t0004a0001c0001t0005a0001c0001t0017others(84): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
5_prime_UTR_variant | MODIFIER | c.-59T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/22 | 59 | chr7 | 2559123 | |||||
| chr7:2559176
|
G | T | 3 | a0001c0022t0090a0001c0022t0091a0007c0039t0092 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
5_prime_UTR_variant | MODIFIER | c.-6G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/22 | 6 | chr7 | 2559176 | |||||
| chr7:2610185
|
C | T | 73 | a0002c0002t0002a0002c0002t0003a0002c0002t0013others(70): Show | 205 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*23C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 23 | chr7 | 2610185 | |||||
| chr7:2610298
|
T | G | 44 | a0001c0029t0051a0002c0002t0002a0002c0002t0003others(41): Show | 144 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*136T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 136 | chr7 | 2610298 | |||||
| chr7:2610442
|
G | T | 5 | a0005c0007t0007a0005c0007t0089a0005c0007t0115others(2): Show | 13 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*280G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 280 | chr7 | 2610442 | |||||
| chr7:2610467
|
C | T | 1 | a0001c0001t0071 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*305C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 305 | chr7 | 2610467 | |||||
| chr7:2610589
|
G | C | 51 | a0002c0002t0002a0002c0002t0003a0002c0002t0013others(48): Show | 162 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*427G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 427 | chr7 | 2610589 | |||||
| chr7:2610739
|
C | T | 17 | a0001c0003t0027a0001c0022t0091a0004c0008t0010others(14): Show | 32 | HG00639.hp2 HG01081.hp1 HG01496.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*577C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 577 | chr7 | 2610739 | |||||
| chr7:2610746
|
C | T | 4 | a0007c0016t0035a0007c0016t0050a0007c0016t0079others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*584C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 584 | chr7 | 2610746 | |||||
| chr7:2610875
|
T | TATAATC | 73 | a0001c0029t0051a0002c0002t0002a0002c0002t0003others(70): Show | 205 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*714_*715insTAATCA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 715 | INFO_REALIGN_3_PRIME | chr7 | 2610875 | ||||
| chr7:2610940
|
G | A | 1 | a0004c0008t0064 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*778G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 778 | chr7 | 2610940 | |||||
| chr7:2610997
|
G | A | 3 | a0006c0009t0102a0006c0048t0065a0018c0050t0066 | 3 | HG00639.hp2 HG02258.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*835G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 835 | chr7 | 2610997 | |||||
| chr7:2611004
|
C | T | 2 | a0004c0008t0064a0004c0008t0070 | 2 | HG02970.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*842C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 842 | chr7 | 2611004 | |||||
| chr7:2611027
|
G | C | 1 | a0015c0031t0103 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*865G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 865 | chr7 | 2611027 | |||||
| chr7:2611030
|
C | T | 3 | a0001c0003t0027a0001c0022t0091a0014c0018t0034 | 6 | HG01496.hp2 HG02451.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*868C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 868 | chr7 | 2611030 | |||||
| chr7:2611089
|
C | A | 3 | a0006c0009t0102a0006c0048t0065a0018c0050t0066 | 3 | HG00639.hp2 HG02258.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*927C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 927 | chr7 | 2611089 | |||||
| chr7:2611103
|
A | G | 1 | a0018c0050t0066 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*941A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 941 | chr7 | 2611103 | |||||
| chr7:2611110
|
T | TGGCTG | 26 | a0001c0010t0009a0001c0010t0053a0001c0034t0009others(23): Show | 58 | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*977_*981dupTGGGC | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 982 | INFO_REALIGN_3_PRIME | chr7 | 2611110 | ||||
| chr7:2611110
|
T | TGGCTGGG others(3): Show |
5 | a0001c0001t0097a0001c0003t0027a0001c0022t0091others(2): Show | 8 | HG01496.hp2 HG02451.hp1 HG02896.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*972_*981dupTGGGCT others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 982 | INFO_REALIGN_3_PRIME | chr7 | 2611110 | ||||
| chr7:2611110
|
T | TGGCTGGG others(8): Show |
8 | a0001c0001t0031a0001c0001t0055a0006c0009t0014others(5): Show | 13 | HG00639.hp2 HG01081.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*967_*981dupTGGGCT others(9): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 982 | INFO_REALIGN_3_PRIME | chr7 | 2611110 | ||||
| chr7:2611110
|
T | TGGCTGGG others(13): Show |
15 | a0001c0001t0005a0001c0001t0006a0001c0001t0021others(12): Show | 40 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*962_*981dupTGGGCT others(14): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 982 | INFO_REALIGN_3_PRIME | chr7 | 2611110 | ||||
| chr7:2611110
|
T | TGGCTGGG others(18): Show |
9 | a0001c0001t0017a0001c0001t0059a0001c0001t0060others(6): Show | 15 | HG02027.hp1 HG02280.hp2 HG02717.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*957_*981dupTGGGCT others(19): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 982 | INFO_REALIGN_3_PRIME | chr7 | 2611110 | ||||
| chr7:2611110
|
T | TGGCTGGG others(23): Show |
2 | a0001c0001t0061a0001c0001t0062 | 2 | HG03139.hp1 NA18956.hp1 |
3_prime_UTR_variant | MODIFIER | c.*952_*981dupTGGGCT others(24): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 982 | INFO_REALIGN_3_PRIME | chr7 | 2611110 | ||||
| chr7:2611110
|
T | TGGCTGGG others(28): Show |
1 | a0001c0001t0063 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*981_*982insTGGGCT others(29): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 982 | INFO_REALIGN_3_PRIME | chr7 | 2611110 | ||||
| chr7:2611110
|
TGGCTG | T | 2 | a0001c0001t0052a0001c0003t0026 | 4 | HG06807.hp1 NA19043.hp2 NA20805.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*977_*981delTGGGC | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 977 | INFO_REALIGN_3_PRIME | chr7 | 2611110 | ||||
| chr7:2611124
|
T | TGGGCCGG others(3): Show |
2 | a0002c0002t0018a0023c0043t0018 | 4 | NA18995.hp2 NA19002.hp2 NA19070.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*966_*967insCGGGCC others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 967 | INFO_REALIGN_3_PRIME | chr7 | 2611124 | ||||
| chr7:2611129
|
T | C | 2 | a0002c0002t0018a0023c0043t0018 | 4 | NA18995.hp2 NA19002.hp2 NA19070.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*967T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 967 | chr7 | 2611129 | |||||
| chr7:2611129
|
T | TGGGCCGG others(3): Show |
39 | a0001c0029t0051a0002c0002t0002a0002c0002t0003others(36): Show | 137 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*971_*972insCGGGCC others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 972 | INFO_REALIGN_3_PRIME | chr7 | 2611129 | ||||
| chr7:2611129
|
T | TGGGGCCG others(4): Show |
1 | a0002c0002t0078 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*970_*971insGCCGGG others(5): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 971 | INFO_REALIGN_3_PRIME | chr7 | 2611129 | ||||
| chr7:2611129
|
TGGGCTGG others(8): Show |
T | 1 | a0003c0005t0110 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*972_*986delTGGGCT others(9): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 972 | INFO_REALIGN_3_PRIME | chr7 | 2611129 | ||||
| chr7:2611134
|
T | C | 42 | a0001c0029t0051a0002c0002t0002a0002c0002t0003others(39): Show | 142 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*972T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 972 | chr7 | 2611134 | |||||
| chr7:2611134
|
T | TGGGCCGG others(28): Show |
1 | a0001c0003t0020 | 3 | HG02895.hp2 HG02897.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*976_*977insCGGGCC others(29): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 977 | INFO_REALIGN_3_PRIME | chr7 | 2611134 | ||||
| chr7:2611134
|
TGGGCTGG others(3): Show |
T | 5 | a0003c0020t0083a0003c0020t0084a0008c0006t0023others(2): Show | 7 | HG01167.hp2 HG01243.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*977_*986delTGGGCC others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 977 | INFO_REALIGN_3_PRIME | chr7 | 2611134 | ||||
| chr7:2611139
|
T | C | 40 | a0001c0003t0020a0001c0003t0026a0001c0029t0051others(37): Show | 143 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*977T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 977 | chr7 | 2611139 | |||||
| chr7:2611139
|
T | TGGGCCGG others(28): Show |
2 | a0001c0003t0030a0001c0022t0090 | 3 | HG01891.hp2 HG02258.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*986_*987insCGGGCC others(29): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 987 | INFO_REALIGN_3_PRIME | chr7 | 2611139 | ||||
| chr7:2611139
|
TGGGCC | T | 5 | a0005c0007t0007a0005c0007t0089a0005c0007t0115others(2): Show | 13 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*982_*986delCGGGC | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 982 | INFO_REALIGN_3_PRIME | chr7 | 2611139 | ||||
| chr7:2611143
|
C | CTGGGCTG others(13): Show |
3 | a0001c0001t0037a0001c0001t0054a0001c0001t0098 | 4 | HG00741.hp2 HG01257.hp1 HG01884.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*981_*982insTGGGCT others(14): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 982 | chr7 | 2611143 | |||||
| chr7:2611144
|
C | T | 65 | a0001c0001t0005a0001c0001t0006a0001c0001t0017others(62): Show | 132 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*982C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 982 | chr7 | 2611144 | |||||
| chr7:2611207
|
C | T | 1 | a0002c0002t0076 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1045C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1045 | chr7 | 2611207 | |||||
| chr7:2611211
|
C | T | 1 | a0006c0009t0102 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1049C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1049 | chr7 | 2611211 | |||||
| chr7:2611281
|
T | G | 1 | a0001c0003t0093 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1119T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1119 | chr7 | 2611281 | |||||
| chr7:2611292
|
G | A | 5 | a0005c0007t0007a0005c0007t0089a0005c0007t0115others(2): Show | 13 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1130G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1130 | chr7 | 2611292 | |||||
| chr7:2611429
|
A | T | 2 | a0006c0009t0014a0006c0009t0117 | 6 | HG01081.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1267A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1267 | chr7 | 2611429 | |||||
| chr7:2611439
|
T | C | 1 | a0001c0001t0056 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1277T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1277 | chr7 | 2611439 | |||||
| chr7:2611456
|
T | C | 1 | a0019c0051t0081 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1294T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1294 | chr7 | 2611456 | |||||
| chr7:2611503
|
G | T | 1 | a0002c0002t0075 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1341G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1341 | chr7 | 2611503 | |||||
| chr7:2611534
|
T | G | 102 | a0001c0001t0005a0001c0001t0006a0001c0001t0017others(99): Show | 264 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*1372T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1372 | chr7 | 2611534 | |||||
| chr7:2611547
|
C | T | 1 | a0006c0009t0102 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1385C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1385 | chr7 | 2611547 | |||||
| chr7:2611639
|
G | A | 3 | a0001c0010t0009a0001c0010t0053a0001c0034t0009 | 8 | HG01192.hp2 HG01243.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1477G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1477 | chr7 | 2611639 | |||||
| chr7:2611641
|
G | A | 1 | a0004c0008t0010 | 7 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1479G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1479 | chr7 | 2611641 | |||||
| chr7:2611674
|
C | CA | 50 | a0001c0029t0051a0002c0002t0002a0002c0002t0003others(47): Show | 161 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*1513dupA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1514 | INFO_REALIGN_3_PRIME | chr7 | 2611674 | ||||
| chr7:2611787
|
G | C | 49 | a0001c0029t0051a0002c0002t0002a0002c0002t0003others(46): Show | 160 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*1625G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1625 | chr7 | 2611787 | |||||
| chr7:2611910
|
G | T | 2 | a0009c0013t0022a0009c0013t0068 | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1748G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1748 | chr7 | 2611910 | |||||
| chr7:2611925
|
G | A | 1 | a0001c0001t0097 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1763G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1763 | chr7 | 2611925 | |||||
| chr7:2611928
|
C | T | 2 | a0001c0001t0058a0001c0001t0099 | 2 | HG00438.hp1 NA18947.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1766C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1766 | chr7 | 2611928 | |||||
| chr7:2611929
|
G | A | 23 | a0003c0005t0008a0003c0005t0011a0003c0005t0025others(20): Show | 44 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1767G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1767 | chr7 | 2611929 | |||||
| chr7:2612005
|
A | G | 90 | a0001c0003t0027a0001c0022t0091a0001c0029t0051others(87): Show | 237 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*1843A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1843 | chr7 | 2612005 | |||||
| chr7:2612090
|
T | C | 2 | a0009c0013t0022a0009c0013t0068 | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1928T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 1928 | chr7 | 2612090 | |||||
| chr7:2612240
|
G | A | 1 | a0003c0005t0041 | 2 | HG00642.hp1 HG00642.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2078G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2078 | chr7 | 2612240 | |||||
| chr7:2612257
|
C | A | 1 | a0002c0004t0072 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2095C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2095 | chr7 | 2612257 | |||||
| chr7:2612287
|
C | T | 28 | a0001c0001t0038a0002c0049t0073a0003c0005t0008others(25): Show | 59 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2125C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2125 | chr7 | 2612287 | |||||
| chr7:2612362
|
C | T | 16 | a0003c0005t0008a0003c0005t0025a0003c0005t0041others(13): Show | 31 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2200C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2200 | chr7 | 2612362 | |||||
| chr7:2612388
|
TG | T | 5 | a0004c0028t0067a0006c0009t0014a0006c0009t0117others(2): Show | 9 | HG01081.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2228delG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2228 | INFO_REALIGN_3_PRIME | chr7 | 2612388 | ||||
| chr7:2612433
|
G | A | 1 | a0005c0007t0089 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2271G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2271 | chr7 | 2612433 | |||||
| chr7:2612452
|
C | T | 2 | a0006c0009t0014a0006c0009t0117 | 6 | HG01081.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2290C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2290 | chr7 | 2612452 | |||||
| chr7:2612464
|
C | T | 1 | a0001c0010t0053 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2302C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2302 | chr7 | 2612464 | |||||
| chr7:2612498
|
A | C | 1 | a0001c0001t0048 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2336A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2336 | chr7 | 2612498 | |||||
| chr7:2612527
|
C | CCATGGGA others(26): Show |
1 | a0001c0001t0094 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2394_*2426dupCTAG others(29): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2427 | INFO_REALIGN_3_PRIME | chr7 | 2612527 | ||||
| chr7:2612572
|
TGAGCTGT others(9): Show |
T | 48 | a0001c0001t0005a0001c0001t0006a0001c0001t0017others(45): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2421_*2436delCGGG others(12): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2421 | INFO_REALIGN_3_PRIME | chr7 | 2612572 | ||||
| chr7:2612576
|
C | A | 48 | a0001c0001t0055a0002c0002t0002a0002c0002t0003others(45): Show | 163 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*2414C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2414 | chr7 | 2612576 | |||||
| chr7:2612588
|
C | T | 4 | a0001c0003t0036a0001c0003t0096a0006c0009t0014others(1): Show | 9 | HG00099.hp1 HG01081.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2426C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2426 | chr7 | 2612588 | |||||
| chr7:2612655
|
A | C | 1 | a0006c0009t0102 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2493A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2493 | chr7 | 2612655 | |||||
| chr7:2612716
|
A | AGGTGAGC others(26): Show |
1 | a0001c0003t0036 | 2 | HG00099.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2567_*2599dupGCGG others(29): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2600 | INFO_REALIGN_3_PRIME | chr7 | 2612716 | ||||
| chr7:2612766
|
G | C | 2 | a0007c0012t0019a0007c0012t0080 | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2604G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2604 | chr7 | 2612766 | |||||
| chr7:2612888
|
G | A | 1 | a0001c0001t0059 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2726G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2726 | chr7 | 2612888 | |||||
| chr7:2612896
|
C | T | 1 | a0003c0005t0112 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2734C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2734 | chr7 | 2612896 | |||||
| chr7:2612979
|
C | T | 2 | a0009c0013t0022a0009c0013t0068 | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2817C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2817 | chr7 | 2612979 | |||||
| chr7:2612996
|
G | A | 18 | a0001c0001t0005a0001c0001t0006a0001c0001t0028others(15): Show | 43 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2834G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2834 | chr7 | 2612996 | |||||
| chr7:2613034
|
A | T | 1 | a0001c0001t0048 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2872A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2872 | chr7 | 2613034 | |||||
| chr7:2613146
|
A | T | 1 | a0008c0006t0086 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2984A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2984 | chr7 | 2613146 | |||||
| chr7:2613154
|
C | T | 1 | a0007c0039t0092 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2992C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 2992 | chr7 | 2613154 | |||||
| chr7:2613170
|
C | T | 1 | a0001c0001t0057 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3008C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3008 | chr7 | 2613170 | |||||
| chr7:2613204
|
C | T | 7 | a0001c0001t0032a0001c0030t0032a0005c0007t0007others(4): Show | 15 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3042C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3042 | chr7 | 2613204 | |||||
| chr7:2613243
|
C | T | 7 | a0001c0001t0032a0001c0030t0032a0005c0007t0007others(4): Show | 15 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3081C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3081 | chr7 | 2613243 | |||||
| chr7:2613394
|
G | A | 54 | a0001c0001t0032a0001c0001t0058a0001c0001t0099others(51): Show | 169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*3232G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3232 | chr7 | 2613394 | |||||
| chr7:2613493
|
A | G | 1 | a0001c0001t0048 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3331A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3331 | chr7 | 2613493 | |||||
| chr7:2613517
|
C | T | 2 | a0006c0036t0033a0006c0044t0033 | 2 | HG02145.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3355C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3355 | chr7 | 2613517 | |||||
| chr7:2613707
|
C | T | 1 | a0003c0005t0042 | 2 | HG01981.hp1 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3545C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3545 | chr7 | 2613707 | |||||
| chr7:2613719
|
A | G | 3 | a0001c0003t0027a0001c0022t0091a0014c0018t0034 | 6 | HG01496.hp2 HG02451.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3557A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3557 | chr7 | 2613719 | |||||
| chr7:2613777
|
C | T | 1 | a0001c0001t0048 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3615C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3615 | chr7 | 2613777 | |||||
| chr7:2613778
|
T | C | 1 | a0001c0001t0048 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3616T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3616 | chr7 | 2613778 | |||||
| chr7:2613869
|
C | G | 1 | a0001c0001t0048 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3707C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3707 | chr7 | 2613869 | |||||
| chr7:2613870
|
C | G | 22 | a0003c0005t0008a0003c0005t0011a0003c0005t0025others(19): Show | 43 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3708C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3708 | chr7 | 2613870 | |||||
| chr7:2613937
|
C | T | 22 | a0003c0005t0008a0003c0005t0011a0003c0005t0025others(19): Show | 43 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3775C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3775 | chr7 | 2613937 | |||||
| chr7:2613945
|
G | A | 22 | a0003c0005t0008a0003c0005t0011a0003c0005t0025others(19): Show | 43 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3783G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3783 | chr7 | 2613945 | |||||
| chr7:2613948
|
A | G | 22 | a0003c0005t0008a0003c0005t0011a0003c0005t0025others(19): Show | 43 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3786A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3786 | chr7 | 2613948 | |||||
| chr7:2614016
|
T | G | 1 | a0001c0001t0048 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3854T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3854 | chr7 | 2614016 | |||||
| chr7:2614023
|
C | T | 1 | a0001c0003t0095 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3861C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3861 | chr7 | 2614023 | |||||
| chr7:2614074
|
G | A | 2 | a0007c0012t0019a0007c0012t0080 | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3912G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3912 | chr7 | 2614074 | |||||
| chr7:2614099
|
C | T | 2 | a0006c0009t0102a0006c0048t0065 | 2 | HG00639.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3937C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3937 | chr7 | 2614099 | |||||
| chr7:2614125
|
C | CA | 29 | a0001c0010t0009a0001c0010t0053a0001c0034t0009others(26): Show | 55 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*3971dupA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3972 | INFO_REALIGN_3_PRIME | chr7 | 2614125 | ||||
| chr7:2614158
|
C | A | 52 | a0001c0001t0032a0001c0001t0058a0001c0001t0099others(49): Show | 163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*3996C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 3996 | chr7 | 2614158 | |||||
| chr7:2614239
|
C | T | 1 | a0009c0013t0068 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4077C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 4077 | chr7 | 2614239 | |||||
| chr7:2614286
|
C | T | 1 | a0001c0001t0062 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4124C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 4124 | chr7 | 2614286 | |||||
| chr7:2614364
|
T | G | 1 | a0001c0001t0048 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4202T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 4202 | chr7 | 2614364 | |||||
| chr7:2614412
|
C | T | 1 | a0002c0002t0105 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4250C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 4250 | chr7 | 2614412 | |||||
| chr7:2614416
|
C | T | 3 | a0001c0010t0009a0001c0010t0053a0001c0034t0009 | 8 | HG01192.hp2 HG01243.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4254C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 22/22 | 4254 | chr7 | 2614416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2559236
|
G | A | 1 | a0008c0006t0023g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.36+19G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559236 | ||||||
| chr7:2559274
|
T | C | 199 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(196): Show | 201 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.36+57T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559274 | ||||||
| chr7:2559276
|
C | T | 1 | a0001c0011t0001g0413 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.36+59C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559276 | ||||||
| chr7:2559289
|
C | T | 4 | a0001c0001t0001g0410a0001c0001t0001g0411a0001c0001t0001g0412others(1): Show | 4 | HG02083.hp1 NA18612.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+72C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559289 | ||||||
| chr7:2559488
|
A | C | 2 | a0004c0008t0064g0197a0004c0008t0070g0198 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.36+271A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559488 | ||||||
| chr7:2559628
|
T | C | 1 | a0001c0010t0009g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.36+411T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559628 | ||||||
| chr7:2559692
|
A | G | 409 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(406): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.36+475A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559692 | ||||||
| chr7:2559707
|
A | G | 1 | a0001c0001t0005g0408 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.36+490A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559707 | ||||||
| chr7:2559720
|
A | G | 91 | a0001c0001t0004g0173a0001c0001t0004g0180a0001c0001t0004g0183others(88): Show | 92 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.36+503A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559720 | ||||||
| chr7:2559765
|
T | TG | 35 | a0001c0001t0001g0397a0001c0001t0001g0410a0001c0001t0001g0411others(32): Show | 35 | HG00438.hp2 HG01123.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.36+565dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2559765 | |||||
| chr7:2559765
|
TG | T | 48 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0268others(45): Show | 48 | HG00280.hp2 HG00423.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.36+565delG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2559765 | |||||
| chr7:2559765
|
TGG | T | 45 | a0001c0001t0001g0208a0001c0001t0001g0210a0001c0001t0001g0237others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.36+564_36+565delGG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2559765 | |||||
| chr7:2559765
|
TGGG | T | 51 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(48): Show | 51 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.36+563_36+565delGG others(1): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2559765 | |||||
| chr7:2559765
|
TGGGG | T | 57 | a0001c0001t0001g0218a0001c0001t0004g0063a0001c0001t0004g0072others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.36+562_36+565delGG others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2559765 | |||||
| chr7:2559765
|
TGGGGG | T | 72 | a0001c0001t0001g0215a0001c0001t0004g0026a0001c0001t0004g0027others(69): Show | 72 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.36+561_36+565delGG others(3): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2559765 | |||||
| chr7:2559765
|
TGGGGGG | T | 26 | a0001c0001t0062g0113a0001c0003t0020g0021a0002c0002t0002g0006others(23): Show | 27 | HG01192.hp1 HG01884.hp1 HG02280.hp1 others(24): Show |
intron_variant | MODIFIER | c.36+560_36+565delGG others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2559765 | |||||
| chr7:2559768
|
G | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02004.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.36+551G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559768 | ||||||
| chr7:2559769
|
G | C | 3 | a0001c0001t0001g0208a0001c0001t0001g0210a0002c0002t0039g0209 | 3 | HG00544.hp2 HG02273.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.36+552G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559769 | ||||||
| chr7:2559770
|
G | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG01943.hp1 HG01952.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+553G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559770 | ||||||
| chr7:2559894
|
T | C | 1 | a0002c0049t0073g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.36+677T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559894 | ||||||
| chr7:2559984
|
C | T | 1 | a0002c0002t0002g0053 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.36+767C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559984 | ||||||
| chr7:2559985
|
C | G | 1 | a0006c0044t0033g0085 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.36+768C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2559985 | ||||||
| chr7:2560231
|
A | G | 13 | a0001c0003t0020g0021a0004c0008t0010g0015a0004c0008t0010g0016others(10): Show | 13 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.36+1014A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2560231 | ||||||
| chr7:2560442
|
A | G | 96 | a0001c0001t0004g0173a0001c0001t0004g0180a0001c0001t0004g0183others(93): Show | 97 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.36+1225A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2560442 | ||||||
| chr7:2560623
|
A | G | 1 | a0001c0003t0001g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.36+1406A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2560623 | ||||||
| chr7:2560649
|
T | C | 15 | a0001c0001t0017g0083a0001c0001t0031g0116a0001c0003t0004g0099others(12): Show | 15 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.36+1432T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2560649 | ||||||
| chr7:2560655
|
T | A | 1 | a0002c0002t0002g0055 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.36+1438T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2560655 | ||||||
| chr7:2560670
|
TCTCTTGG others(13): Show |
T | 9 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0004t0002g0001others(6): Show | 10 | HG00609.hp1 HG03688.hp1 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.36+1457_36+1476del others(20): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2560670 | |||||
| chr7:2560716
|
G | T | 1 | a0003c0005t0011g0050 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.36+1499G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2560716 | ||||||
| chr7:2560825
|
C | T | 14 | a0001c0001t0037g0372a0001c0001t0037g0376a0001c0001t0098g0371others(11): Show | 14 | HG00099.hp2 HG01255.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.36+1608C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2560825 | ||||||
| chr7:2560955
|
C | CA | 127 | a0001c0001t0001g0205a0001c0001t0001g0222a0001c0001t0001g0224others(124): Show | 128 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.36+1760dupA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2560955 | |||||
| chr7:2560955
|
C | CAA | 31 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0063others(28): Show | 31 | HG00621.hp2 HG01255.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.36+1759_36+1760dup others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2560955 | |||||
| chr7:2560955
|
CA | C | 11 | a0001c0001t0001g0215a0001c0001t0038g0367a0001c0003t0001g0368others(8): Show | 11 | HG01109.hp2 HG02258.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.36+1760delA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2560955 | |||||
| chr7:2561012
|
C | G | 1 | a0001c0003t0030g0048 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.36+1795C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561012 | ||||||
| chr7:2561058
|
AAGGATTC others(101): Show |
A | 92 | a0001c0001t0004g0173a0001c0001t0004g0180a0001c0001t0004g0183others(89): Show | 93 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.36+1845_36+1952del | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2561058 | |||||
| chr7:2561079
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.36+1862T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561079 | ||||||
| chr7:2561137
|
T | C | 3 | a0001c0001t0001g0225a0001c0001t0001g0268a0002c0004t0003g0213 | 3 | HG00597.hp1 NA18980.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.36+1920T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561137 | ||||||
| chr7:2561220
|
A | G | 8 | a0001c0003t0026g0365a0001c0003t0026g0386a0002c0004t0003g0406others(5): Show | 8 | HG01081.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+2003A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561220 | ||||||
| chr7:2561282
|
A | G | 2 | a0002c0002t0002g0153a0002c0002t0002g0158 | 2 | NA18968.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.36+2065A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561282 | ||||||
| chr7:2561385
|
T | C | 213 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(210): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.36+2168T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561385 | ||||||
| chr7:2561422
|
A | AT | 13 | a0001c0001t0017g0152a0001c0001t0048g0242a0001c0022t0090g0082others(10): Show | 13 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.36+2221dupT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2561422 | |||||
| chr7:2561422
|
AT | A | 17 | a0001c0001t0005g0175a0001c0001t0100g0199a0001c0003t0020g0021others(14): Show | 17 | HG01109.hp2 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.36+2221delT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2561422 | |||||
| chr7:2561484
|
G | A | 1 | a0003c0005t0042g0369 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.36+2267G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561484 | ||||||
| chr7:2561506
|
C | T | 1 | a0002c0004t0003g0364 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.36+2289C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561506 | ||||||
| chr7:2561548
|
G | A | 1 | a0002c0002t0002g0055 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.36+2331G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561548 | ||||||
| chr7:2561565
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0006g0255 | 2 | HG03669.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.36+2348C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561565 | ||||||
| chr7:2561575
|
C | G | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.36+2358C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561575 | ||||||
| chr7:2561716
|
C | T | 5 | a0001c0003t0020g0118a0001c0003t0020g0119a0001c0003t0030g0155others(2): Show | 5 | HG02258.hp2 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.36+2499C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561716 | ||||||
| chr7:2561726
|
A | G | 76 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(73): Show | 77 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.36+2509A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561726 | ||||||
| chr7:2561857
|
A | G | 7 | a0001c0001t0032g0079a0001c0003t0004g0098a0001c0019t0004g0093others(4): Show | 7 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.36+2640A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561857 | ||||||
| chr7:2561878
|
A | C | 59 | a0001c0001t0001g0225a0001c0001t0001g0268a0001c0001t0001g0299others(56): Show | 59 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.36+2661A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561878 | ||||||
| chr7:2561952
|
A | C | 4 | a0001c0001t0101g0235a0001c0003t0026g0234a0002c0004t0003g0257others(1): Show | 4 | HG01255.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+2735A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561952 | ||||||
| chr7:2561974
|
C | A | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.36+2757C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2561974 | ||||||
| chr7:2562038
|
A | G | 4 | a0001c0003t0020g0118a0001c0003t0020g0119a0001c0003t0030g0155others(1): Show | 4 | HG02258.hp2 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+2821A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562038 | ||||||
| chr7:2562133
|
A | G | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.36+2916A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562133 | ||||||
| chr7:2562146
|
A | G | 1 | a0003c0005t0114g0251 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.36+2929A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562146 | ||||||
| chr7:2562148
|
CAT | C | 4 | a0001c0003t0020g0021a0004c0008t0010g0022a0004c0008t0010g0052others(1): Show | 4 | HG02145.hp2 HG03471.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+2934_36+2935del others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2562148 | |||||
| chr7:2562233
|
G | GGT | 143 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0036others(140): Show | 145 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.36+3034_36+3035dup others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2562233 | |||||
| chr7:2562235
|
T | G | 18 | a0001c0003t0020g0021a0001c0010t0009g0005a0002c0004t0002g0109others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.36+3018T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562235 | ||||||
| chr7:2562285
|
C | CAT | 10 | a0001c0003t0020g0021a0001c0003t0020g0118a0001c0003t0020g0119others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.36+3084_36+3085dup others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2562285 | |||||
| chr7:2562285
|
C | CATATAT | 6 | a0001c0001t0017g0083a0001c0003t0004g0099a0006c0044t0033g0085others(3): Show | 6 | HG02886.hp1 HG03453.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.36+3080_36+3085dup others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2562285 | |||||
| chr7:2562285
|
C | CATATATA others(3): Show |
51 | a0001c0001t0004g0173a0001c0001t0004g0180a0001c0001t0005g0166others(48): Show | 52 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.36+3076_36+3085dup others(10): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2562285 | |||||
| chr7:2562285
|
C | CATATATA others(5): Show |
16 | a0001c0001t0004g0183a0001c0001t0017g0144a0001c0001t0031g0142others(13): Show | 16 | HG01167.hp2 HG01978.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.36+3074_36+3085dup others(12): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2562285 | |||||
| chr7:2562285
|
C | CATATATA others(7): Show |
12 | a0001c0001t0017g0152a0001c0001t0062g0113a0001c0001t0063g0150others(9): Show | 12 | HG01192.hp1 HG02572.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.36+3072_36+3085dup others(14): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2562285 | |||||
| chr7:2562285
|
C | CATATATA others(13): Show |
1 | a0008c0006t0024g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.36+3085_36+3086ins others(20): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2562285 | |||||
| chr7:2562558
|
T | C | 1 | a0002c0049t0073g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.36+3341T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562558 | ||||||
| chr7:2562571
|
A | G | 1 | a0001c0019t0004g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.36+3354A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562571 | ||||||
| chr7:2562593
|
C | CT | 6 | a0001c0001t0001g0347a0002c0002t0003g0362a0002c0004t0003g0290others(3): Show | 6 | HG01175.hp2 HG02080.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.36+3389dupT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2562593 | |||||
| chr7:2562593
|
CT | C | 89 | a0001c0001t0001g0225a0001c0001t0001g0412a0001c0001t0004g0026others(86): Show | 90 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.36+3389delT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2562593 | |||||
| chr7:2562605
|
T | C | 2 | a0004c0008t0064g0197a0004c0008t0070g0198 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.36+3388T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562605 | ||||||
| chr7:2562606
|
T | C | 9 | a0001c0001t0062g0113a0004c0008t0064g0197a0004c0008t0070g0198others(6): Show | 9 | HG01192.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.36+3389T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562606 | ||||||
| chr7:2562621
|
G | T | 1 | a0002c0002t0003g0362 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.36+3404G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562621 | ||||||
| chr7:2562717
|
A | G | 2 | a0001c0003t0001g0346a0001c0003t0001g0368 | 2 | HG02071.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.36+3500A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562717 | ||||||
| chr7:2562785
|
T | G | 1 | a0001c0001t0099g0305 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.36+3568T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562785 | ||||||
| chr7:2562786
|
A | G | 4 | a0001c0001t0017g0152a0001c0001t0063g0150a0007c0016t0079g0145others(1): Show | 4 | HG01167.hp2 HG02970.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+3569A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562786 | ||||||
| chr7:2562814
|
A | G | 409 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(406): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.36+3597A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562814 | ||||||
| chr7:2562855
|
C | CT | 17 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0032g0079others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.36+3650dupT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2562855 | |||||
| chr7:2562958
|
C | T | 1 | a0002c0004t0002g0109 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.36+3741C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562958 | ||||||
| chr7:2562990
|
A | G | 1 | a0008c0006t0023g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.36+3773A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2562990 | ||||||
| chr7:2563042
|
C | T | 15 | a0001c0001t0037g0372a0001c0001t0037g0376a0001c0001t0098g0371others(12): Show | 15 | HG00099.hp2 HG01255.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.36+3825C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563042 | ||||||
| chr7:2563043
|
G | A | 2 | a0006c0009t0014g0267a0006c0009t0014g0303 | 2 | HG01081.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.36+3826G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563043 | ||||||
| chr7:2563078
|
A | G | 1 | a0002c0002t0003g0302 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.36+3861A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563078 | ||||||
| chr7:2563104
|
T | G | 1 | a0001c0003t0004g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.36+3887T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563104 | ||||||
| chr7:2563201
|
C | T | 14 | a0001c0001t0001g0343a0001c0003t0001g0313a0001c0003t0095g0345others(11): Show | 14 | HG00140.hp1 HG00621.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.37-3915C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563201 | ||||||
| chr7:2563374
|
G | GTT | 3 | a0002c0049t0073g0054a0008c0006t0024g0127a0019c0051t0081g0128 | 3 | HG02965.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.37-3741_37-3740dup others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563374 | |||||
| chr7:2563375
|
T | TTG | 31 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(28): Show | 31 | HG00544.hp2 HG00642.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.37-3705_37-3704dup others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563375
|
T | TTGTG | 18 | a0001c0001t0001g0210a0001c0001t0006g0233a0001c0001t0006g0250others(15): Show | 18 | HG01257.hp1 HG01515.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.37-3707_37-3704dup others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563375
|
T | TTGTGTG | 3 | a0001c0003t0001g0260a0001c0010t0009g0005a0002c0004t0108g0259 | 3 | HG01243.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.37-3709_37-3704dup others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563375
|
T | TTGTGTGT others(3): Show |
2 | a0001c0022t0090g0082a0001c0022t0091g0081 | 2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.37-3713_37-3704dup others(10): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563375
|
T | TTTTG | 61 | a0001c0001t0004g0173a0001c0001t0004g0180a0001c0001t0004g0183others(58): Show | 62 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.37-3740_37-3739ins others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563375
|
T | TTTTGTG | 16 | a0001c0001t0017g0140a0001c0001t0017g0144a0001c0001t0031g0116others(13): Show | 16 | HG01192.hp2 HG02145.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.37-3740_37-3739ins others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563375
|
T | TTTTGTGT others(3): Show |
12 | a0001c0001t0005g0057a0001c0003t0020g0021a0002c0002t0029g0031others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.37-3740_37-3739ins others(10): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563375
|
T | TTTTGTGT others(5): Show |
69 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(66): Show | 70 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.37-3740_37-3739ins others(12): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563375
|
T | TTTTGTGT others(7): Show |
8 | a0001c0001t0004g0047a0001c0003t0020g0118a0001c0003t0020g0119others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.37-3740_37-3739ins others(14): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563375
|
T | TTTTGTGT others(9): Show |
4 | a0001c0003t0030g0155a0002c0002t0002g0141a0007c0012t0019g0120others(1): Show | 4 | HG02258.hp2 HG02895.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-3740_37-3739ins others(16): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563375
|
T | TTTTGTGT others(13): Show |
1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.37-3740_37-3739ins others(20): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563375
|
TTG | T | 78 | a0001c0001t0001g0268a0001c0001t0001g0299a0001c0001t0001g0397others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.37-3705_37-3704del others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563375
|
TTGTGTGT others(7): Show |
T | 1 | a0013c0024t0001g0201 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.37-3717_37-3704del others(14): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563375 | |||||
| chr7:2563377
|
G | A | 1 | a0002c0002t0002g0141 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.37-3739G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563377 | ||||||
| chr7:2563379
|
G | A | 5 | a0001c0001t0004g0047a0001c0003t0030g0048a0001c0029t0051g0171others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-3737G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563379 | ||||||
| chr7:2563381
|
G | A | 63 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(60): Show | 64 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.37-3735G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563381 | ||||||
| chr7:2563383
|
G | A | 12 | a0001c0001t0005g0057a0001c0003t0020g0021a0002c0002t0029g0031others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.37-3733G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563383 | ||||||
| chr7:2563409
|
G | C | 3 | a0001c0001t0031g0116a0006c0036t0033g0172a0009c0013t0022g0154 | 3 | HG02145.hp1 HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.37-3707G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563409 | ||||||
| chr7:2563411
|
G | A | 5 | a0001c0003t0020g0118a0001c0003t0020g0119a0001c0003t0030g0155others(2): Show | 5 | HG02258.hp2 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.37-3705G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563411 | ||||||
| chr7:2563413
|
A | T | 1 | a0002c0002t0003g0362 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.37-3703A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563413 | ||||||
| chr7:2563475
|
C | T | 1 | a0003c0005t0112g0373 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.37-3641C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563475 | ||||||
| chr7:2563562
|
T | A | 5 | a0001c0003t0020g0118a0001c0003t0020g0119a0001c0003t0030g0155others(2): Show | 5 | HG02258.hp2 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.37-3554T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563562 | ||||||
| chr7:2563575
|
T | G | 6 | a0001c0001t0017g0083a0001c0003t0004g0099a0006c0044t0033g0085others(3): Show | 6 | HG02886.hp1 HG03453.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-3541T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563575 | ||||||
| chr7:2563653
|
C | T | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.37-3463C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563653 | ||||||
| chr7:2563669
|
C | T | 1 | a0002c0004t0003g0213 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.37-3447C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563669 | ||||||
| chr7:2563726
|
C | T | 3 | a0001c0001t0006g0332a0001c0003t0001g0333a0001c0003t0016g0311 | 3 | HG02165.hp2 NA18948.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.37-3390C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563726 | ||||||
| chr7:2563769
|
C | G | 1 | a0013c0024t0001g0203 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.37-3347C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563769 | ||||||
| chr7:2563811
|
G | A | 1 | a0001c0001t0099g0305 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.37-3305G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563811 | ||||||
| chr7:2563893
|
C | CA | 152 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(149): Show | 154 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.37-3200dupA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563893 | |||||
| chr7:2563893
|
C | CAA | 31 | a0001c0001t0017g0083a0001c0001t0017g0152a0001c0001t0021g0129others(28): Show | 31 | HG00099.hp2 HG01255.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.37-3201_37-3200dup others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563893 | |||||
| chr7:2563893
|
CA | C | 12 | a0001c0001t0001g0207a0001c0003t0001g0333a0001c0003t0036g0247others(9): Show | 12 | HG00609.hp2 HG02622.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.37-3200delA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2563893 | |||||
| chr7:2563917
|
T | A | 6 | a0001c0010t0009g0005a0002c0004t0002g0109a0002c0015t0002g0075others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-3199T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563917 | ||||||
| chr7:2563967
|
T | G | 1 | a0001c0019t0004g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.37-3149T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2563967 | ||||||
| chr7:2564025
|
T | C | 1 | a0002c0049t0073g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.37-3091T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564025 | ||||||
| chr7:2564039
|
C | T | 5 | a0001c0003t0020g0118a0001c0003t0020g0119a0001c0003t0030g0155others(2): Show | 5 | HG02258.hp2 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.37-3077C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564039 | ||||||
| chr7:2564134
|
G | C | 213 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(210): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.37-2982G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564134 | ||||||
| chr7:2564143
|
C | T | 1 | a0001c0001t0004g0045 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.37-2973C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564143 | ||||||
| chr7:2564260
|
G | T | 91 | a0001c0001t0004g0173a0001c0001t0004g0180a0001c0001t0004g0183others(88): Show | 92 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.37-2856G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564260 | ||||||
| chr7:2564326
|
G | T | 1 | a0002c0002t0002g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.37-2790G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564326 | ||||||
| chr7:2564332
|
C | G | 1 | a0002c0004t0003g0257 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.37-2784C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564332 | ||||||
| chr7:2564399
|
AG | A | 6 | a0001c0010t0009g0005a0002c0004t0002g0109a0002c0015t0002g0075others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-2716delG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564399 | ||||||
| chr7:2564424
|
C | T | 37 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0032g0079others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.37-2692C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564424 | ||||||
| chr7:2564503
|
C | A | 2 | a0004c0008t0064g0197a0004c0008t0070g0198 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.37-2613C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564503 | ||||||
| chr7:2564506
|
G | C | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.37-2610G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564506 | ||||||
| chr7:2564523
|
G | A | 4 | a0001c0003t0020g0118a0001c0003t0020g0119a0001c0003t0030g0155others(1): Show | 4 | HG02258.hp2 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-2593G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564523 | ||||||
| chr7:2564624
|
GA | G | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.37-2490delA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2564624 | |||||
| chr7:2564686
|
T | C | 5 | a0001c0003t0020g0118a0001c0003t0020g0119a0001c0003t0030g0155others(2): Show | 5 | HG02258.hp2 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.37-2430T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564686 | ||||||
| chr7:2564708
|
C | T | 1 | a0002c0002t0002g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.37-2408C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564708 | ||||||
| chr7:2564844
|
C | T | 17 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0032g0079others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.37-2272C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564844 | ||||||
| chr7:2564860
|
C | T | 1 | a0001c0003t0001g0331 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.37-2256C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564860 | ||||||
| chr7:2564880
|
G | A | 6 | a0001c0001t0031g0116a0001c0022t0090g0082a0001c0022t0091g0081others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.37-2236G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564880 | ||||||
| chr7:2564881
|
C | T | 1 | a0003c0005t0114g0251 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.37-2235C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564881 | ||||||
| chr7:2564980
|
C | G | 1 | a0006c0009t0117g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.37-2136C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2564980 | ||||||
| chr7:2565020
|
G | C | 1 | a0001c0001t0006g0388 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.37-2096G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565020 | ||||||
| chr7:2565027
|
C | T | 80 | a0001c0001t0004g0173a0001c0001t0004g0180a0001c0001t0004g0183others(77): Show | 81 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.37-2089C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565027 | ||||||
| chr7:2565093
|
T | TGTGC | 94 | a0001c0001t0004g0173a0001c0001t0004g0180a0001c0001t0004g0183others(91): Show | 95 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.37-2019_37-2016dup others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2565093 | |||||
| chr7:2565097
|
CGT | C | 6 | a0002c0002t0002g0074a0002c0002t0015g0316a0002c0002t0015g0321others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.37-2007_37-2006del others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2565097 | |||||
| chr7:2565133
|
A | AGT | 69 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(66): Show | 70 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.37-1963_37-1962dup others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2565133 | |||||
| chr7:2565133
|
A | AGTGT | 3 | a0001c0001t0004g0072a0001c0001t0006g0226a0001c0001t0006g0236 | 3 | HG00597.hp2 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.37-1965_37-1962dup others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2565133 | |||||
| chr7:2565133
|
A | AGTGTGT | 14 | a0001c0003t0020g0021a0001c0029t0051g0171a0004c0008t0010g0015others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.37-1967_37-1962dup others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2565133 | |||||
| chr7:2565133
|
A | AGTGTGTG others(3): Show |
1 | a0008c0006t0082g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.37-1971_37-1962dup others(10): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2565133 | |||||
| chr7:2565133
|
AGT | A | 35 | a0001c0001t0001g0211a0001c0001t0001g0241a0001c0001t0004g0047others(32): Show | 35 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.37-1963_37-1962del others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2565133 | |||||
| chr7:2565133
|
AGTGT | A | 85 | a0001c0001t0004g0173a0001c0001t0004g0180a0001c0001t0004g0183others(82): Show | 86 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.37-1965_37-1962del others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2565133 | |||||
| chr7:2565182
|
C | T | 17 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0032g0079others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.37-1934C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565182 | ||||||
| chr7:2565228
|
AGTGT | A | 3 | a0001c0001t0031g0116a0006c0036t0033g0172a0009c0013t0022g0154 | 3 | HG02145.hp1 HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.37-1882_37-1879del others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2565228 | |||||
| chr7:2565235
|
GTGCGTGT others(11): Show |
G | 1 | a0002c0004t0013g0256 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.37-1863_37-1846del others(18): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2565235 | |||||
| chr7:2565242
|
T | C | 77 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(74): Show | 78 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.37-1874T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565242 | ||||||
| chr7:2565256
|
C | T | 13 | a0001c0001t0037g0372a0001c0001t0037g0376a0001c0001t0098g0371others(10): Show | 13 | HG00099.hp2 HG01255.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.37-1860C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565256 | ||||||
| chr7:2565256
|
CGT | C | 80 | a0001c0001t0004g0173a0001c0001t0004g0180a0001c0001t0004g0183others(77): Show | 81 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.37-1848_37-1847del others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2565256 | |||||
| chr7:2565332
|
C | T | 6 | a0001c0010t0009g0005a0002c0004t0002g0109a0002c0015t0002g0075others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-1784C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565332 | ||||||
| chr7:2565345
|
G | A | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.37-1771G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565345 | ||||||
| chr7:2565363
|
A | G | 50 | a0001c0001t0001g0205a0001c0001t0004g0026a0001c0001t0004g0027others(47): Show | 50 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.37-1753A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565363 | ||||||
| chr7:2565378
|
C | G | 8 | a0001c0001t0001g0343a0001c0003t0001g0313a0001c0011t0001g0314others(5): Show | 8 | HG00140.hp1 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.37-1738C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565378 | ||||||
| chr7:2565421
|
G | T | 1 | a0001c0010t0009g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.37-1695G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565421 | ||||||
| chr7:2565430
|
G | A | 63 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(60): Show | 64 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.37-1686G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565430 | ||||||
| chr7:2565464
|
C | G | 1 | a0002c0049t0073g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.37-1652C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565464 | ||||||
| chr7:2565699
|
G | A | 214 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(211): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.37-1417G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565699 | ||||||
| chr7:2565735
|
C | T | 2 | a0003c0005t0025g0003a0003c0005t0025g0167 | 3 | HG01069.hp1 HG01071.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.37-1381C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565735 | ||||||
| chr7:2565781
|
A | T | 6 | a0001c0001t0017g0083a0001c0003t0004g0099a0006c0044t0033g0085others(3): Show | 6 | HG02886.hp1 HG03453.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-1335A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565781 | ||||||
| chr7:2565790
|
A | G | 17 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0032g0079others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.37-1326A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565790 | ||||||
| chr7:2565793
|
T | C | 1 | a0002c0004t0108g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.37-1323T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565793 | ||||||
| chr7:2565896
|
T | G | 1 | a0001c0003t0036g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.37-1220T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2565896 | ||||||
| chr7:2566159
|
A | C | 1 | a0002c0049t0073g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.37-957A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566159 | ||||||
| chr7:2566256
|
G | C | 2 | a0001c0003t0001g0324a0001c0003t0001g0389 | 2 | NA18969.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.37-860G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566256 | ||||||
| chr7:2566271
|
C | G | 17 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0032g0079others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.37-845C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566271 | ||||||
| chr7:2566271
|
C | T | 185 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(182): Show | 187 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(184): Show |
intron_variant | MODIFIER | c.37-845C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566271 | ||||||
| chr7:2566292
|
C | CT | 93 | a0001c0001t0001g0347a0001c0001t0004g0180a0001c0001t0005g0166others(90): Show | 94 | HG00408.hp2 HG00639.hp2 HG00741.hp1 others(91): Show |
intron_variant | MODIFIER | c.37-809dupT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2566292 | |||||
| chr7:2566292
|
CT | C | 52 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(49): Show | 52 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.37-809delT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2566292 | |||||
| chr7:2566318
|
G | A | 1 | a0001c0001t0005g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.37-798G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566318 | ||||||
| chr7:2566393
|
A | G | 10 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(7): Show | 11 | HG01069.hp1 HG01071.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.37-723A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566393 | ||||||
| chr7:2566455
|
G | GT | 69 | a0001c0001t0001g0210a0001c0001t0001g0218a0001c0001t0001g0224others(66): Show | 69 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.37-641dupT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2566455 | |||||
| chr7:2566455
|
G | GTT | 8 | a0001c0001t0005g0103a0001c0001t0032g0079a0001c0003t0030g0155others(5): Show | 8 | HG00140.hp2 HG01978.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.37-642_37-641dupTT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2566455 | |||||
| chr7:2566455
|
GT | G | 62 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(59): Show | 63 | HG00558.hp1 HG00609.hp1 HG01257.hp2 others(60): Show |
intron_variant | MODIFIER | c.37-641delT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 2566455 | |||||
| chr7:2566456
|
T | TC | 12 | a0001c0003t0020g0021a0001c0029t0051g0171a0004c0008t0010g0016others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.37-660_37-659insC | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566456 | ||||||
| chr7:2566457
|
T | C | 12 | a0001c0001t0004g0043a0001c0001t0004g0072a0001c0003t0030g0048others(9): Show | 12 | HG00597.hp2 HG00621.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.37-659T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566457 | ||||||
| chr7:2566458
|
T | C | 56 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0030others(53): Show | 57 | HG00558.hp1 HG00609.hp1 HG01257.hp2 others(54): Show |
intron_variant | MODIFIER | c.37-658T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566458 | ||||||
| chr7:2566459
|
T | TG | 4 | a0002c0002t0003g0301a0002c0002t0003g0362a0002c0004t0003g0269others(1): Show | 4 | HG00423.hp2 HG02080.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-657_37-656insG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566459 | ||||||
| chr7:2566460
|
T | G | 68 | a0001c0001t0001g0225a0001c0001t0001g0268a0001c0001t0001g0397others(65): Show | 68 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.37-656T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566460 | ||||||
| chr7:2566892
|
G | T | 18 | a0001c0003t0020g0118a0001c0003t0020g0119a0001c0010t0009g0122others(15): Show | 18 | HG02083.hp2 HG02451.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.37-224G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566892 | ||||||
| chr7:2566929
|
C | G | 4 | a0001c0022t0090g0082a0001c0022t0091g0081a0006c0009t0014g0387others(1): Show | 4 | HG02451.hp1 HG02818.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-187C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566929 | ||||||
| chr7:2566946
|
A | G | 1 | a0001c0022t0090g0082 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.37-170A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2566946 | ||||||
| chr7:2567033
|
G | A | 1 | a0001c0001t0071g0032 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.37-83G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2567033 | ||||||
| chr7:2567045
|
C | G | 1 | a0001c0001t0031g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.37-71C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2567045 | ||||||
| chr7:2567083
|
G | A | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.37-33G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 1/21 | chr7 | 2567083 | ||||||
| chr7:2567207
|
C | T | 1 | a0004c0008t0010g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.84+44C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567207 | ||||||
| chr7:2567229
|
C | T | 1 | a0017c0033t0012g0320 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.84+66C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567229 | ||||||
| chr7:2567248
|
G | A | 3 | a0002c0002t0003g0349a0002c0002t0003g0350a0002c0002t0003g0404 | 3 | NA18945.hp1 NA18956.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.84+85G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567248 | ||||||
| chr7:2567257
|
A | G | 4 | a0002c0002t0003g0232a0002c0014t0003g0231a0002c0014t0003g0248others(1): Show | 4 | NA18942.hp2 NA19002.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+94A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567257 | ||||||
| chr7:2567300
|
G | A | 44 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(41): Show | 44 | HG00438.hp2 HG00558.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.84+137G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567300 | ||||||
| chr7:2567303
|
G | A | 19 | a0001c0019t0004g0093a0001c0019t0004g0105a0002c0045t0029g0080others(16): Show | 19 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.84+140G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567303 | ||||||
| chr7:2567423
|
C | T | 2 | a0011c0021t0040g0370a0011c0021t0040g0374 | 2 | HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.84+260C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567423 | ||||||
| chr7:2567454
|
C | G | 1 | a0001c0003t0001g0368 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.84+291C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567454 | ||||||
| chr7:2567493
|
G | A | 1 | a0002c0004t0002g0161 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.84+330G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567493 | ||||||
| chr7:2567518
|
C | T | 1 | a0002c0002t0075g0089 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.84+355C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567518 | ||||||
| chr7:2567556
|
C | T | 5 | a0002c0049t0073g0054a0007c0016t0035g0143a0007c0016t0050g0266others(2): Show | 5 | HG02109.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+393C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567556 | ||||||
| chr7:2567618
|
A | G | 271 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(268): Show | 272 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.84+455A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567618 | ||||||
| chr7:2567625
|
C | T | 11 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.84+462C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567625 | ||||||
| chr7:2567703
|
G | C | 3 | a0001c0001t0031g0116a0001c0001t0031g0142a0001c0001t0055g0170 | 3 | HG02109.hp1 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.84+540G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567703 | ||||||
| chr7:2567705
|
G | A | 163 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(160): Show | 163 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.84+542G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567705 | ||||||
| chr7:2567727
|
G | C | 4 | a0001c0010t0009g0005a0002c0015t0002g0075a0002c0015t0002g0076others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+564G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567727 | ||||||
| chr7:2567767
|
G | A | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.84+604G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567767 | ||||||
| chr7:2567772
|
C | T | 9 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(6): Show | 9 | HG01496.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.84+609C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567772 | ||||||
| chr7:2567834
|
C | T | 105 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(102): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.84+671C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567834 | ||||||
| chr7:2567853
|
C | A | 1 | a0001c0003t0004g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.84+690C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2567853 | ||||||
| chr7:2568014
|
C | T | 2 | a0001c0001t0100g0199a0027c0052t0001g0344 | 2 | HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.84+851C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568014 | ||||||
| chr7:2568017
|
G | A | 5 | a0002c0049t0073g0054a0007c0016t0035g0143a0007c0016t0050g0266others(2): Show | 5 | HG02109.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+854G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568017 | ||||||
| chr7:2568261
|
A | T | 152 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(149): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.85-693A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568261 | ||||||
| chr7:2568395
|
C | T | 1 | a0001c0003t0001g0270 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.85-559C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568395 | ||||||
| chr7:2568416
|
G | A | 4 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0061others(1): Show | 4 | NA18944.hp2 NA18978.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-538G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568416 | ||||||
| chr7:2568446
|
C | T | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-508C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568446 | ||||||
| chr7:2568469
|
T | C | 1 | a0002c0004t0107g0289 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.85-485T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568469 | ||||||
| chr7:2568535
|
T | C | 242 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(239): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.85-419T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568535 | ||||||
| chr7:2568543
|
A | T | 259 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(256): Show | 260 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.85-411A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568543 | ||||||
| chr7:2568551
|
C | T | 2 | a0004c0008t0064g0197a0004c0008t0070g0198 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.85-403C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568551 | ||||||
| chr7:2568626
|
G | A | 255 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(252): Show | 256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.85-328G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568626 | ||||||
| chr7:2568638
|
G | A | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.85-316G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568638 | ||||||
| chr7:2568763
|
C | T | 1 | a0002c0004t0003g0213 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.85-191C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568763 | ||||||
| chr7:2568826
|
C | T | 1 | a0001c0001t0037g0372 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.85-128C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568826 | ||||||
| chr7:2568833
|
G | A | 10 | a0002c0002t0002g0126a0002c0002t0002g0133a0002c0002t0002g0134others(7): Show | 10 | NA18943.hp2 NA18950.hp1 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.85-121G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568833 | ||||||
| chr7:2568877
|
T | C | 1 | a0001c0001t0016g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.85-77T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568877 | ||||||
| chr7:2568898
|
G | A | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.85-56G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 2/21 | chr7 | 2568898 | ||||||
| chr7:2569050
|
C | T | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.130+51C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569050 | ||||||
| chr7:2569081
|
C | T | 1 | a0001c0001t0052g0060 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.130+82C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569081 | ||||||
| chr7:2569148
|
C | T | 1 | a0013c0024t0001g0201 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.130+149C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569148 | ||||||
| chr7:2569200
|
C | T | 8 | a0001c0003t0095g0345a0001c0010t0009g0121a0001c0010t0009g0122others(5): Show | 8 | HG01192.hp2 HG02486.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.130+201C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569200 | ||||||
| chr7:2569206
|
G | A | 102 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(99): Show | 103 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.130+207G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569206 | ||||||
| chr7:2569213
|
T | C | 45 | a0001c0003t0020g0021a0001c0003t0020g0118a0001c0003t0020g0119others(42): Show | 45 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.130+214T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569213 | ||||||
| chr7:2569255
|
C | T | 12 | a0001c0003t0020g0021a0001c0003t0020g0118a0001c0003t0020g0119others(9): Show | 12 | HG01192.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+256C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569255 | ||||||
| chr7:2569276
|
C | T | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.130+277C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569276 | ||||||
| chr7:2569313
|
C | G | 2 | a0004c0008t0064g0197a0004c0008t0070g0198 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.130+314C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569313 | ||||||
| chr7:2569415
|
G | T | 11 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+416G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569415 | ||||||
| chr7:2569419
|
C | T | 1 | a0003c0005t0008g0182 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.130+420C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569419 | ||||||
| chr7:2569619
|
G | A | 1 | a0004c0028t0067g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.130+620G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569619 | ||||||
| chr7:2569675
|
A | G | 44 | a0001c0003t0020g0021a0001c0003t0020g0118a0001c0003t0020g0119others(41): Show | 44 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.130+676A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569675 | ||||||
| chr7:2569695
|
C | T | 11 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+696C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569695 | ||||||
| chr7:2569788
|
A | G | 1 | a0006c0036t0033g0172 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.130+789A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569788 | ||||||
| chr7:2569868
|
G | A | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.130+869G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569868 | ||||||
| chr7:2569990
|
C | T | 12 | a0001c0003t0020g0021a0001c0003t0020g0118a0001c0003t0020g0119others(9): Show | 12 | HG01192.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+991C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2569990 | ||||||
| chr7:2570079
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.130+1080C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2570079 | ||||||
| chr7:2570131
|
C | T | 224 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(221): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.130+1132C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2570131 | ||||||
| chr7:2570144
|
G | C | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+1145G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2570144 | ||||||
| chr7:2570170
|
T | C | 6 | a0001c0029t0051g0171a0002c0049t0073g0054a0007c0016t0035g0143others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+1171T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2570170 | ||||||
| chr7:2570246
|
G | C | 1 | a0002c0002t0002g0153 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.130+1247G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2570246 | ||||||
| chr7:2570263
|
T | C | 1 | a0001c0001t0063g0150 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.131-1263T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2570263 | ||||||
| chr7:2570302
|
C | T | 2 | a0013c0024t0001g0201a0013c0024t0001g0203 | 2 | HG01123.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.131-1224C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2570302 | ||||||
| chr7:2570327
|
C | T | 6 | a0001c0029t0051g0171a0002c0049t0073g0054a0007c0016t0035g0143others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-1199C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2570327 | ||||||
| chr7:2570336
|
C | T | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.131-1190C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2570336 | ||||||
| chr7:2570339
|
C | T | 3 | a0001c0003t0001g0333a0001c0003t0004g0071a0001c0003t0016g0311 | 3 | NA18948.hp1 NA18961.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.131-1187C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2570339 | ||||||
| chr7:2570459
|
G | C | 267 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(264): Show | 269 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.131-1067G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2570459 | ||||||
| chr7:2570769
|
C | T | 88 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.131-757C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2570769 | ||||||
| chr7:2571022
|
A | ATTCTT | 18 | a0001c0019t0004g0093a0001c0019t0004g0105a0005c0007t0007g0002others(15): Show | 18 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.131-488_131-484dup others(5): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr7 | 2571022 | |||||
| chr7:2571127
|
C | G | 1 | a0001c0003t0001g0312 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.131-399C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2571127 | ||||||
| chr7:2571194
|
T | A | 2 | a0002c0004t0003g0221a0002c0004t0003g0261 | 2 | NA19057.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.131-332T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2571194 | ||||||
| chr7:2571194
|
T | C | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.131-332T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2571194 | ||||||
| chr7:2571244
|
C | T | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.131-282C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2571244 | ||||||
| chr7:2571256
|
C | T | 7 | a0002c0002t0002g0074a0002c0002t0002g0156a0002c0002t0015g0316others(4): Show | 7 | HG01256.hp2 HG01258.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-270C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2571256 | ||||||
| chr7:2571281
|
G | C | 1 | a0001c0003t0095g0345 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.131-245G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2571281 | ||||||
| chr7:2571284
|
A | G | 2 | a0001c0047t0001g0308a0006c0048t0065g0165 | 2 | HG00639.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.131-242A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2571284 | ||||||
| chr7:2571312
|
C | G | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.131-214C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2571312 | ||||||
| chr7:2571320
|
C | G | 5 | a0001c0003t0026g0234a0001c0003t0026g0365a0001c0003t0026g0386others(2): Show | 5 | HG01891.hp2 HG06807.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-206C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2571320 | ||||||
| chr7:2571358
|
A | G | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.131-168A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 3/21 | chr7 | 2571358 | ||||||
| chr7:2571708
|
A | G | 4 | a0001c0001t0094g0409a0001c0003t0001g0270a0001c0003t0001g0377others(1): Show | 4 | HG02083.hp1 NA18979.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+54A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 4/21 | chr7 | 2571708 | ||||||
| chr7:2571778
|
G | A | 27 | a0001c0019t0004g0093a0001c0019t0004g0105a0004c0008t0010g0015others(24): Show | 27 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.259+124G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 4/21 | chr7 | 2571778 | ||||||
| chr7:2571800
|
G | A | 28 | a0001c0019t0004g0093a0001c0019t0004g0105a0001c0029t0051g0171others(25): Show | 28 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.259+146G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 4/21 | chr7 | 2571800 | ||||||
| chr7:2571875
|
A | G | 28 | a0001c0019t0004g0093a0001c0019t0004g0105a0001c0029t0051g0171others(25): Show | 28 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.259+221A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 4/21 | chr7 | 2571875 | ||||||
| chr7:2571913
|
T | C | 1 | a0002c0002t0076g0065 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.259+259T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 4/21 | chr7 | 2571913 | ||||||
| chr7:2571988
|
C | T | 1 | a0021c0027t0047g0243 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.260-204C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 4/21 | chr7 | 2571988 | ||||||
| chr7:2572020
|
G | T | 27 | a0001c0019t0004g0093a0001c0019t0004g0105a0004c0008t0010g0015others(24): Show | 27 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.260-172G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 4/21 | chr7 | 2572020 | ||||||
| chr7:2572063
|
G | T | 1 | a0001c0001t0001g0205 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.260-129G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 4/21 | chr7 | 2572063 | ||||||
| chr7:2572100
|
C | T | 1 | a0015c0031t0103g0296 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.260-92C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 4/21 | chr7 | 2572100 | ||||||
| chr7:2572120
|
T | C | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.260-72T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 4/21 | chr7 | 2572120 | ||||||
| chr7:2572430
|
C | T | 1 | a0001c0010t0053g0137 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.394+104C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2572430 | ||||||
| chr7:2572528
|
C | T | 1 | a0006c0036t0033g0172 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.394+202C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2572528 | ||||||
| chr7:2572531
|
C | T | 14 | a0001c0003t0020g0021a0001c0003t0020g0118a0001c0003t0020g0119others(11): Show | 14 | HG00639.hp2 HG01192.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.394+205C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2572531 | ||||||
| chr7:2572589
|
G | A | 13 | a0001c0003t0020g0021a0001c0003t0020g0118a0001c0003t0020g0119others(10): Show | 13 | HG00639.hp2 HG01192.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.394+263G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2572589 | ||||||
| chr7:2572660
|
T | A | 108 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(105): Show | 109 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.394+334T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2572660 | ||||||
| chr7:2572661
|
C | A | 108 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(105): Show | 109 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.394+335C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2572661 | ||||||
| chr7:2572689
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.394+363T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2572689 | ||||||
| chr7:2572701
|
T | C | 28 | a0001c0019t0004g0093a0001c0019t0004g0105a0001c0029t0051g0171others(25): Show | 28 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.394+375T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2572701 | ||||||
| chr7:2572717
|
C | T | 2 | a0001c0047t0001g0308a0006c0048t0065g0165 | 2 | HG00639.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.394+391C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2572717 | ||||||
| chr7:2572732
|
C | T | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.394+406C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2572732 | ||||||
| chr7:2572740
|
C | T | 13 | a0001c0003t0020g0021a0001c0003t0020g0118a0001c0003t0020g0119others(10): Show | 13 | HG00639.hp2 HG01192.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.394+414C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2572740 | ||||||
| chr7:2572962
|
G | A | 28 | a0001c0019t0004g0093a0001c0019t0004g0105a0001c0029t0051g0171others(25): Show | 28 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.395-456G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2572962 | ||||||
| chr7:2573173
|
T | C | 28 | a0001c0019t0004g0093a0001c0019t0004g0105a0001c0029t0051g0171others(25): Show | 28 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.395-245T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2573173 | ||||||
| chr7:2573177
|
C | T | 1 | a0011c0021t0040g0370 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.395-241C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2573177 | ||||||
| chr7:2573233
|
C | G | 266 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(263): Show | 268 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.395-185C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2573233 | ||||||
| chr7:2573374
|
A | G | 28 | a0001c0019t0004g0093a0001c0019t0004g0105a0001c0029t0051g0171others(25): Show | 28 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.395-44A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2573374 | ||||||
| chr7:2573408
|
G | C | 248 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(245): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.395-10G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 5/21 | chr7 | 2573408 | ||||||
| chr7:2573499
|
G | A | 13 | a0005c0007t0007g0002a0005c0007t0007g0067a0005c0007t0007g0101others(10): Show | 13 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.465+11G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573499 | ||||||
| chr7:2573523
|
C | T | 2 | a0001c0003t0027g0272a0003c0005t0088g0164 | 2 | NA19003.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.465+35C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573523 | ||||||
| chr7:2573583
|
G | T | 12 | a0001c0029t0051g0171a0004c0008t0010g0015a0004c0008t0010g0016others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.465+95G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573583 | ||||||
| chr7:2573669
|
G | A | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.465+181G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573669 | ||||||
| chr7:2573695
|
G | A | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.465+207G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573695 | ||||||
| chr7:2573790
|
T | G | 204 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(201): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.465+302T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573790 | ||||||
| chr7:2573907
|
G | T | 12 | a0001c0029t0051g0171a0004c0008t0010g0015a0004c0008t0010g0016others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.465+419G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573907 | ||||||
| chr7:2573909
|
C | T | 1 | a0001c0001t0031g0116 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.465+421C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573909 | ||||||
| chr7:2573910
|
G | A | 28 | a0001c0019t0004g0093a0001c0019t0004g0105a0001c0029t0051g0171others(25): Show | 28 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.465+422G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573910 | ||||||
| chr7:2573930
|
A | G | 12 | a0008c0006t0023g0004a0008c0006t0023g0107a0008c0006t0023g0146others(9): Show | 12 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.465+442A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573930 | ||||||
| chr7:2573935
|
A | C | 268 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(265): Show | 270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.465+447A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573935 | ||||||
| chr7:2573936
|
G | A | 12 | a0008c0006t0023g0004a0008c0006t0023g0107a0008c0006t0023g0146others(9): Show | 12 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.465+448G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573936 | ||||||
| chr7:2573939
|
T | G | 33 | a0002c0004t0002g0001a0002c0004t0002g0007a0002c0004t0002g0008others(30): Show | 34 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.465+451T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2573939 | ||||||
| chr7:2573964
|
C | CG | 4 | a0007c0016t0035g0143a0007c0016t0050g0266a0007c0016t0079g0145others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+477dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2573964 | |||||
| chr7:2574051
|
T | C | 12 | a0001c0029t0051g0171a0004c0008t0010g0015a0004c0008t0010g0016others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.465+563T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2574051 | ||||||
| chr7:2574120
|
G | A | 12 | a0001c0029t0051g0171a0004c0008t0010g0015a0004c0008t0010g0016others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.465+632G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2574120 | ||||||
| chr7:2574148
|
G | A | 13 | a0001c0003t0020g0021a0001c0003t0020g0118a0001c0003t0020g0119others(10): Show | 13 | HG00639.hp2 HG01192.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.465+660G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2574148 | ||||||
| chr7:2574203
|
T | G | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.465+715T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2574203 | ||||||
| chr7:2574213
|
C | G | 268 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(265): Show | 270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.465+725C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2574213 | ||||||
| chr7:2574219
|
C | G | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.465+731C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2574219 | ||||||
| chr7:2574310
|
C | T | 1 | a0006c0036t0033g0172 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.465+822C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2574310 | ||||||
| chr7:2574330
|
G | A | 1 | a0001c0011t0001g0413 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.465+842G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2574330 | ||||||
| chr7:2574448
|
G | C | 28 | a0001c0019t0004g0093a0001c0019t0004g0105a0001c0029t0051g0171others(25): Show | 28 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.465+960G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2574448 | ||||||
| chr7:2574535
|
C | T | 27 | a0001c0029t0051g0171a0004c0008t0010g0015a0004c0008t0010g0016others(24): Show | 27 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.465+1047C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2574535 | ||||||
| chr7:2574780
|
C | T | 25 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.465+1292C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2574780 | ||||||
| chr7:2574791
|
G | A | 2 | a0002c0002t0002g0073a0002c0002t0002g0087 | 2 | HG02698.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.465+1303G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2574791 | ||||||
| chr7:2575159
|
C | T | 1 | a0002c0049t0073g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.465+1671C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575159 | ||||||
| chr7:2575172
|
C | T | 3 | a0001c0001t0006g0332a0001c0001t0038g0328a0001c0003t0004g0174 | 3 | HG00738.hp2 HG02015.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.465+1684C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575172 | ||||||
| chr7:2575182
|
T | C | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.465+1694T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575182 | ||||||
| chr7:2575234
|
A | G | 243 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(240): Show | 245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.465+1746A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575234 | ||||||
| chr7:2575240
|
A | AG | 15 | a0001c0001t0001g0268a0001c0001t0004g0026a0001c0001t0017g0152others(12): Show | 15 | HG00621.hp2 HG01106.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.465+1757dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2575240 | |||||
| chr7:2575250
|
A | G | 254 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(251): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.465+1762A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575250 | ||||||
| chr7:2575488
|
G | A | 98 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(95): Show | 99 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.465+2000G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575488 | ||||||
| chr7:2575555
|
T | G | 256 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(253): Show | 258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.465+2067T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575555 | ||||||
| chr7:2575566
|
G | C | 15 | a0001c0019t0004g0093a0001c0019t0004g0105a0005c0007t0007g0002others(12): Show | 15 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.465+2078G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575566 | ||||||
| chr7:2575579
|
G | GAGT | 3 | a0001c0001t0005g0175a0001c0001t0006g0281a0001c0001t0006g0282 | 3 | HG01109.hp1 HG01169.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.465+2092_465+2094d others(5): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2575579 | |||||
| chr7:2575668
|
C | T | 2 | a0011c0021t0040g0370a0011c0021t0040g0374 | 2 | HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.465+2180C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575668 | ||||||
| chr7:2575683
|
C | T | 5 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0061others(2): Show | 5 | NA18944.hp2 NA18971.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.465+2195C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575683 | ||||||
| chr7:2575688
|
T | C | 2 | a0001c0001t0017g0083a0001c0001t0063g0150 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.465+2200T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575688 | ||||||
| chr7:2575730
|
G | A | 1 | a0001c0003t0004g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.465+2242G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575730 | ||||||
| chr7:2575769
|
A | T | 256 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(253): Show | 258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.465+2281A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575769 | ||||||
| chr7:2575802
|
CA | C | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.465+2315delA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575802 | ||||||
| chr7:2575836
|
G | A | 1 | a0002c0002t0039g0209 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.465+2348G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575836 | ||||||
| chr7:2575857
|
C | T | 43 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(40): Show | 43 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.465+2369C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2575857 | ||||||
| chr7:2576067
|
T | C | 101 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(98): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.466-2175T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2576067 | ||||||
| chr7:2576143
|
C | T | 15 | a0001c0019t0004g0093a0001c0019t0004g0105a0005c0007t0007g0002others(12): Show | 15 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.466-2099C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2576143 | ||||||
| chr7:2576239
|
T | C | 254 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(251): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.466-2003T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2576239 | ||||||
| chr7:2576261
|
G | A | 1 | a0002c0004t0012g0294 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.466-1981G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2576261 | ||||||
| chr7:2576418
|
T | C | 1 | a0007c0037t0035g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.466-1824T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2576418 | ||||||
| chr7:2576814
|
C | A | 2 | a0001c0001t0021g0129a0001c0001t0021g0130 | 2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.466-1428C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2576814 | ||||||
| chr7:2576861
|
C | T | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-1381C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2576861 | ||||||
| chr7:2577112
|
C | T | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-1130C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577112 | ||||||
| chr7:2577126
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.466-1116C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577126 | ||||||
| chr7:2577130
|
G | C | 11 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.466-1112G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577130 | ||||||
| chr7:2577166
|
C | T | 2 | a0001c0047t0001g0308a0006c0048t0065g0165 | 2 | HG00639.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-1076C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577166 | ||||||
| chr7:2577326
|
G | A | 105 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(102): Show | 106 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.466-916G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577326 | ||||||
| chr7:2577332
|
ACATTGGC others(44): Show |
A | 3 | a0001c0003t0004g0174a0013c0024t0001g0201a0013c0024t0001g0203 | 3 | HG00738.hp2 HG01123.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.466-896_466-846del others(51): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577332 | |||||
| chr7:2577343
|
TGCGTGGC others(7): Show |
T | 5 | a0007c0012t0019g0120a0007c0012t0019g0138a0007c0012t0019g0139others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-895_466-882del others(14): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577343 | |||||
| chr7:2577346
|
G | A | 10 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.466-896G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577346 | ||||||
| chr7:2577355
|
C | T | 253 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(250): Show | 255 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.466-887C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577355 | ||||||
| chr7:2577357
|
C | T | 254 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(251): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.466-885C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577357 | ||||||
| chr7:2577380
|
C | CACGCATT others(43): Show |
4 | a0001c0011t0001g0314a0001c0011t0001g0315a0001c0011t0001g0342others(1): Show | 4 | HG00140.hp1 HG01099.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-862_466-861ins others(50): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577380 | ||||||
| chr7:2577381
|
G | A | 10 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.466-861G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577381 | ||||||
| chr7:2577386
|
T | C | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.466-856T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577386 | ||||||
| chr7:2577391
|
G | A | 6 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(3): Show | 6 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-851G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577391 | ||||||
| chr7:2577395
|
G | A | 6 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(3): Show | 6 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-847G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577395 | ||||||
| chr7:2577397
|
A | G | 4 | a0001c0011t0001g0314a0001c0011t0001g0315a0001c0011t0001g0342others(1): Show | 4 | HG00140.hp1 HG01099.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-845A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577397 | ||||||
| chr7:2577397
|
A | T | 6 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(3): Show | 6 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-845A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577397 | ||||||
| chr7:2577406
|
C | T | 4 | a0001c0011t0001g0314a0001c0011t0001g0315a0001c0011t0001g0342others(1): Show | 4 | HG00140.hp1 HG01099.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-836C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577406 | ||||||
| chr7:2577408
|
C | T | 114 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(111): Show | 115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.466-834C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577408 | ||||||
| chr7:2577410
|
C | CG | 6 | a0001c0001t0001g0246a0002c0002t0002g0074a0002c0002t0003g0384others(3): Show | 6 | HG01261.hp1 HG02055.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-828dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577410 | |||||
| chr7:2577416
|
CG | C | 6 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(3): Show | 6 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-825delG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577416 | ||||||
| chr7:2577428
|
G | A | 1 | a0001c0001t0005g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.466-814G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577428 | ||||||
| chr7:2577430
|
G | A | 6 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(3): Show | 6 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-812G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577430 | ||||||
| chr7:2577431
|
C | T | 6 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(3): Show | 6 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-811C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577431 | ||||||
| chr7:2577432
|
A | C | 4 | a0001c0011t0001g0314a0001c0011t0001g0315a0001c0011t0001g0342others(1): Show | 4 | HG00140.hp1 HG01099.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-810A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577432 | ||||||
| chr7:2577442
|
A | G | 269 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.466-800A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577442 | ||||||
| chr7:2577446
|
A | G | 10 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.466-796A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577446 | ||||||
| chr7:2577448
|
T | G | 10 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.466-794T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577448 | ||||||
| chr7:2577448
|
TTGGCTGT others(94): Show |
T | 1 | a0002c0004t0002g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.466-774_466-674del | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577448 | |||||
| chr7:2577454
|
G | C | 1 | a0001c0001t0063g0150 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.466-788G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577454 | ||||||
| chr7:2577457
|
C | T | 6 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(3): Show | 6 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-785C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577457 | ||||||
| chr7:2577459
|
C | T | 6 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(3): Show | 6 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-783C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577459 | ||||||
| chr7:2577461
|
C | CG | 6 | a0001c0001t0006g0255a0001c0001t0031g0142a0001c0001t0099g0305others(3): Show | 6 | HG01255.hp1 HG02615.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-777dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577461 | |||||
| chr7:2577467
|
C | CG | 223 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(220): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.466-775_466-774ins others(1): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577467 | ||||||
| chr7:2577480
|
A | G | 12 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.466-762A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577480 | ||||||
| chr7:2577481
|
T | C | 12 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.466-761T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577481 | ||||||
| chr7:2577482
|
A | ACGCATTG others(44): Show |
1 | a0001c0001t0001g0246 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.466-736_466-735ins others(51): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577482 | |||||
| chr7:2577482
|
A | C | 11 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(8): Show | 11 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.466-760A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577482 | ||||||
| chr7:2577482
|
ACGCATTG others(44): Show |
A | 4 | a0001c0010t0009g0005a0002c0015t0002g0075a0002c0015t0002g0076others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-735_466-685del others(51): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577482 | |||||
| chr7:2577507
|
T | C | 131 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.466-735T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577507 | ||||||
| chr7:2577509
|
T | C | 37 | a0001c0001t0001g0205a0001c0001t0001g0212a0001c0001t0001g0246others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.466-733T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577509 | ||||||
| chr7:2577509
|
T | TGCGGGGA others(44): Show |
3 | a0001c0003t0001g0265a0001c0003t0001g0279a0001c0003t0030g0048 | 3 | HG00735.hp1 HG01069.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.466-658_466-608dup others(51): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577509 | |||||
| chr7:2577511
|
C | CGGGGACG others(45): Show |
1 | a0001c0001t0001g0299 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.466-727_466-676dup others(52): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577511 | |||||
| chr7:2577558
|
C | T | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.466-684C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577558 | ||||||
| chr7:2577562
|
C | CG | 7 | a0001c0003t0001g0377a0001c0029t0051g0171a0002c0002t0002g0029others(4): Show | 7 | HG01109.hp2 HG02004.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-676dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577562 | |||||
| chr7:2577568
|
C | T | 1 | a0001c0001t0100g0199 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.466-674C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577568 | ||||||
| chr7:2577569
|
GTGTGTGC others(197): Show |
G | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.466-660_466-457del | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577569 | |||||
| chr7:2577584
|
C | A | 1 | a0002c0004t0002g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.466-658C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577584 | ||||||
| chr7:2577609
|
C | T | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.466-633C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577609 | ||||||
| chr7:2577613
|
C | CG | 8 | a0001c0001t0001g0222a0001c0001t0004g0072a0002c0002t0003g0318others(5): Show | 8 | HG00597.hp2 HG00642.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.466-625dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577613 | |||||
| chr7:2577624
|
G | A | 25 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.466-618G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577624 | ||||||
| chr7:2577633
|
G | A | 1 | a0002c0004t0002g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.466-609G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577633 | ||||||
| chr7:2577634
|
C | T | 1 | a0002c0004t0002g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.466-608C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577634 | ||||||
| chr7:2577635
|
A | C | 68 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(65): Show | 69 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.466-607A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577635 | ||||||
| chr7:2577650
|
C | T | 2 | a0002c0004t0002g0163a0002c0004t0072g0162 | 2 | HG00639.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.466-592C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577650 | ||||||
| chr7:2577651
|
T | G | 117 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(114): Show | 119 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.466-591T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577651 | ||||||
| chr7:2577651
|
T | TTGGCTGT others(95): Show |
2 | a0007c0016t0035g0143a0007c0016t0079g0145 | 2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.466-559_466-558ins others(102): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577651 | |||||
| chr7:2577651
|
T | TTGGCTGT others(95): Show |
2 | a0001c0029t0051g0171a0002c0049t0073g0054 | 2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.466-559_466-558ins others(102): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577651 | |||||
| chr7:2577651
|
TTGGCTGT others(44): Show |
T | 109 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.466-558_466-508del others(51): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577651 | |||||
| chr7:2577664
|
C | CG | 4 | a0001c0001t0001g0218a0001c0001t0048g0242a0001c0003t0001g0377others(1): Show | 4 | HG01106.hp1 NA18979.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-574dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577664 | |||||
| chr7:2577664
|
C | CGGGGACG others(96): Show |
1 | a0007c0037t0035g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.466-559_466-558ins others(103): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577664 | |||||
| chr7:2577665
|
GGGGACGT others(43): Show |
G | 5 | a0001c0001t0028g0306a0001c0001t0031g0142a0001c0001t0037g0372others(2): Show | 5 | HG01255.hp1 HG01433.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-573_466-524del others(50): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577665 | |||||
| chr7:2577671
|
G | C | 1 | a0002c0004t0002g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.466-571G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577671 | ||||||
| chr7:2577684
|
G | A | 63 | a0001c0001t0001g0299a0001c0001t0004g0180a0001c0001t0052g0060others(60): Show | 64 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.466-558G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577684 | ||||||
| chr7:2577685
|
C | T | 63 | a0001c0001t0001g0299a0001c0001t0004g0180a0001c0001t0052g0060others(60): Show | 64 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.466-557C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577685 | ||||||
| chr7:2577686
|
A | C | 1 | a0001c0001t0001g0212 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.466-556A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577686 | ||||||
| chr7:2577701
|
C | T | 32 | a0001c0001t0001g0299a0001c0001t0052g0060a0002c0004t0002g0001others(29): Show | 33 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.466-541C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577701 | ||||||
| chr7:2577702
|
G | T | 15 | a0001c0001t0005g0102a0001c0001t0006g0233a0001c0001t0006g0250others(12): Show | 16 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.466-540G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577702 | ||||||
| chr7:2577715
|
C | CG | 6 | a0001c0001t0004g0047a0002c0002t0002g0064a0002c0002t0002g0073others(3): Show | 6 | HG00423.hp2 HG00621.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-523dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577715 | |||||
| chr7:2577722
|
G | C | 63 | a0001c0001t0001g0299a0001c0001t0004g0180a0001c0001t0052g0060others(60): Show | 64 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.466-520G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577722 | ||||||
| chr7:2577729
|
C | T | 11 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.466-513C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577729 | ||||||
| chr7:2577735
|
A | G | 13 | a0001c0001t0005g0102a0001c0003t0001g0265a0001c0003t0001g0279others(10): Show | 13 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.466-507A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577735 | ||||||
| chr7:2577736
|
T | C | 13 | a0001c0001t0005g0102a0001c0003t0001g0265a0001c0003t0001g0279others(10): Show | 13 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.466-506T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577736 | ||||||
| chr7:2577737
|
A | C | 6 | a0001c0029t0051g0171a0002c0049t0073g0054a0007c0016t0035g0143others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-505A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577737 | ||||||
| chr7:2577737
|
A | G | 1 | a0002c0004t0002g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.466-505A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577737 | ||||||
| chr7:2577752
|
C | T | 33 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(30): Show | 33 | HG00438.hp2 HG00558.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.466-490C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577752 | ||||||
| chr7:2577773
|
C | G | 30 | a0001c0003t0004g0174a0001c0003t0027g0271a0001c0003t0027g0272others(27): Show | 30 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.466-469C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577773 | ||||||
| chr7:2577773
|
CTGTGTGC others(44): Show |
C | 6 | a0001c0003t0001g0227a0001c0003t0001g0229a0001c0003t0001g0239others(3): Show | 6 | HG04184.hp2 HG04204.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-456_466-406del others(51): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577773 | |||||
| chr7:2577776
|
T | C | 1 | a0002c0004t0002g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.466-466T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577776 | ||||||
| chr7:2577786
|
A | G | 69 | a0001c0001t0001g0299a0001c0001t0004g0180a0001c0001t0052g0060others(66): Show | 70 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.466-456A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577786 | ||||||
| chr7:2577787
|
T | C | 69 | a0001c0001t0001g0299a0001c0001t0004g0180a0001c0001t0052g0060others(66): Show | 70 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.466-455T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577787 | ||||||
| chr7:2577788
|
A | ACGCATTG others(44): Show |
62 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(59): Show | 62 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.466-419_466-418ins others(51): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577788 | |||||
| chr7:2577788
|
A | C | 5 | a0001c0029t0051g0171a0002c0049t0073g0054a0007c0016t0035g0143others(2): Show | 5 | HG01109.hp2 HG02109.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-454A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577788 | ||||||
| chr7:2577788
|
A | G | 63 | a0001c0001t0001g0299a0001c0001t0004g0180a0001c0001t0052g0060others(60): Show | 64 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.466-454A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577788 | ||||||
| chr7:2577788
|
ACGCATTG others(44): Show |
A | 1 | a0001c0003t0016g0311 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.466-403_466-353del others(51): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577788 | |||||
| chr7:2577788
|
ACGCATTG others(95): Show |
A | 1 | a0002c0002t0003g0363 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.466-449_466-348del | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577788 | |||||
| chr7:2577802
|
G | A | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.466-440G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577802 | ||||||
| chr7:2577804
|
G | T | 1 | a0007c0016t0050g0266 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.466-438G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577804 | ||||||
| chr7:2577817
|
C | CG | 5 | a0001c0010t0009g0005a0002c0002t0002g0073a0002c0002t0003g0384others(2): Show | 5 | HG01243.hp1 HG02698.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-421dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577817 | |||||
| chr7:2577817
|
C | CGGGGACG others(96): Show |
1 | a0007c0016t0050g0266 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.466-404_466-403ins others(103): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577817 | |||||
| chr7:2577817
|
C | T | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.466-425C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577817 | ||||||
| chr7:2577820
|
G | A | 9 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(6): Show | 9 | HG01496.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.466-422G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577820 | ||||||
| chr7:2577824
|
G | C | 112 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(109): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.466-418G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577824 | ||||||
| chr7:2577827
|
T | C | 107 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(104): Show | 109 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.466-415T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577827 | ||||||
| chr7:2577839
|
G | C | 23 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(20): Show | 23 | HG00639.hp1 HG01496.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-403G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577839 | ||||||
| chr7:2577844
|
T | G | 23 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(20): Show | 23 | HG00639.hp1 HG01496.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-398T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577844 | ||||||
| chr7:2577847
|
G | T | 23 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(20): Show | 23 | HG00639.hp1 HG01496.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-395G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577847 | ||||||
| chr7:2577858
|
G | A | 1 | a0002c0004t0012g0357 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.466-384G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577858 | ||||||
| chr7:2577861
|
G | C | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.466-381G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577861 | ||||||
| chr7:2577865
|
G | A | 4 | a0007c0012t0019g0120a0007c0012t0019g0138a0007c0012t0019g0168others(1): Show | 4 | HG02809.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-377G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577865 | ||||||
| chr7:2577868
|
C | CG | 6 | a0001c0003t0001g0239a0002c0002t0002g0064a0002c0004t0077g0104others(3): Show | 6 | HG00621.hp2 HG00738.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-370dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577868 | |||||
| chr7:2577878
|
T | C | 213 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(210): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.466-364T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577878 | ||||||
| chr7:2577892
|
G | A | 1 | a0003c0005t0042g0369 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.466-350G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577892 | ||||||
| chr7:2577898
|
T | G | 7 | a0001c0001t0001g0246a0001c0001t0001g0284a0001c0001t0016g0264others(4): Show | 7 | HG00639.hp1 HG02602.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-344T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577898 | ||||||
| chr7:2577916
|
G | A | 106 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.466-326G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577916 | ||||||
| chr7:2577919
|
C | CG | 4 | a0001c0003t0001g0377a0002c0002t0039g0209a0002c0049t0073g0054others(1): Show | 4 | HG00544.hp2 NA18979.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-319dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577919 | |||||
| chr7:2577926
|
G | A | 12 | a0005c0007t0007g0002a0005c0007t0007g0067a0005c0007t0007g0101others(9): Show | 12 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.466-316G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577926 | ||||||
| chr7:2577929
|
T | C | 213 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(210): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.466-313T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577929 | ||||||
| chr7:2577940
|
C | T | 27 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(24): Show | 27 | HG00639.hp1 HG01496.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.466-302C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577940 | ||||||
| chr7:2577941
|
C | G | 135 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(132): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.466-301C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577941 | ||||||
| chr7:2577946
|
G | T | 135 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(132): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.466-296G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577946 | ||||||
| chr7:2577949
|
T | G | 235 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(232): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.466-293T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577949 | ||||||
| chr7:2577949
|
T | TCGTGTGC others(44): Show |
1 | a0002c0049t0073g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.466-252_466-251ins others(51): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577949 | |||||
| chr7:2577955
|
G | A | 27 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(24): Show | 27 | HG00639.hp1 HG01496.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.466-287G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577955 | ||||||
| chr7:2577957
|
G | GTGGCTGT others(19): Show |
4 | a0007c0016t0035g0143a0007c0016t0050g0266a0007c0016t0079g0145others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-272_466-271ins others(26): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577957 | |||||
| chr7:2577957
|
G | GTGGCTGT others(95): Show |
1 | a0006c0009t0102g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.466-263_466-262ins others(102): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577957 | |||||
| chr7:2577957
|
G | GTGGCTGT others(44): Show |
94 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(91): Show | 95 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.466-263_466-262ins others(51): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577957 | |||||
| chr7:2577957
|
G | T | 27 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(24): Show | 27 | HG00639.hp1 HG01496.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.466-285G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577957 | ||||||
| chr7:2577970
|
C | CG | 8 | a0001c0003t0001g0368a0002c0002t0002g0029a0002c0002t0002g0034others(5): Show | 8 | HG00642.hp2 HG01255.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.466-268dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577970 | |||||
| chr7:2577970
|
C | CGGGGACG others(45): Show |
1 | a0001c0001t0001g0224 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.466-263_466-262ins others(52): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2577970 | |||||
| chr7:2577980
|
T | C | 213 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(210): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.466-262T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577980 | ||||||
| chr7:2577991
|
T | C | 7 | a0001c0029t0051g0171a0002c0049t0073g0054a0007c0016t0035g0143others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.466-251T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2577991 | ||||||
| chr7:2578006
|
A | G | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.466-236A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578006 | ||||||
| chr7:2578007
|
C | G | 1 | a0004c0028t0067g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.466-235C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578007 | ||||||
| chr7:2578008
|
T | G | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.466-234T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578008 | ||||||
| chr7:2578021
|
C | CG | 6 | a0001c0001t0037g0372a0001c0003t0001g0377a0001c0010t0053g0137others(3): Show | 6 | HG01261.hp2 HG02523.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-217dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2578021 | |||||
| chr7:2578021
|
C | CGGGGACG others(45): Show |
4 | a0001c0001t0001g0218a0002c0004t0002g0011a0002c0004t0002g0012others(1): Show | 4 | HG03710.hp1 NA18979.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-212_466-211ins others(52): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2578021 | |||||
| chr7:2578021
|
C | CGGGGGAC others(46): Show |
1 | a0001c0001t0001g0412 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.466-217_466-216ins others(53): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2578021 | |||||
| chr7:2578042
|
T | C | 44 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(41): Show | 44 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.466-200T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578042 | ||||||
| chr7:2578057
|
G | A | 1 | a0001c0029t0051g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.466-185G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578057 | ||||||
| chr7:2578059
|
G | T | 1 | a0001c0029t0051g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.466-183G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578059 | ||||||
| chr7:2578068
|
T | C | 11 | a0001c0010t0009g0005a0001c0029t0051g0171a0002c0015t0002g0075others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.466-174T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578068 | ||||||
| chr7:2578091
|
T | C | 11 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.466-151T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578091 | ||||||
| chr7:2578099
|
G | T | 1 | a0001c0029t0051g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.466-143G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578099 | ||||||
| chr7:2578123
|
T | C | 1 | a0001c0029t0051g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.466-119T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578123 | ||||||
| chr7:2578123
|
T | G | 1 | a0019c0051t0081g0128 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.466-119T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578123 | ||||||
| chr7:2578144
|
C | CCCGCATT others(7): Show |
5 | a0002c0049t0073g0054a0007c0016t0035g0143a0007c0016t0050g0266others(2): Show | 5 | HG02109.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-97_466-84dupCC others(12): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2578144 | |||||
| chr7:2578144
|
C | CGCGCAGT others(72): Show |
1 | a0001c0029t0051g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.466-98_466-97insGC others(77): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578144 | ||||||
| chr7:2578153
|
GCGTGTGC others(19): Show |
G | 8 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(5): Show | 8 | HG01496.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.466-82_466-57delCG others(24): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2578153 | |||||
| chr7:2578166
|
T | TGTGTGCG others(18): Show |
1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.466-67_466-43dupGG others(23): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2578166 | |||||
| chr7:2578171
|
G | A | 1 | a0001c0029t0051g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.466-71G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578171 | ||||||
| chr7:2578172
|
C | A | 1 | a0001c0029t0051g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.466-70C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578172 | ||||||
| chr7:2578173
|
G | A | 2 | a0001c0047t0001g0308a0006c0048t0065g0165 | 2 | HG00639.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-69G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | chr7 | 2578173 | ||||||
| chr7:2578174
|
C | CG | 4 | a0001c0001t0061g0176a0001c0003t0001g0239a0001c0003t0001g0377others(1): Show | 4 | HG04204.hp1 NA18950.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-64dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr7 | 2578174 | |||||
| chr7:2578422
|
C | T | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.580-54C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 7/21 | chr7 | 2578422 | ||||||
| chr7:2578436
|
C | CA | 104 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(101): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.580-39dupA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr7 | 2578436 | |||||
| chr7:2578703
|
A | C | 1 | a0002c0002t0002g0064 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.630+177A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2578703 | ||||||
| chr7:2578731
|
A | G | 4 | a0001c0010t0009g0005a0002c0015t0002g0075a0002c0015t0002g0076others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+205A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2578731 | ||||||
| chr7:2578760
|
C | T | 6 | a0001c0010t0009g0121a0001c0010t0009g0122a0001c0010t0009g0124others(3): Show | 6 | HG01192.hp2 HG02486.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.630+234C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2578760 | ||||||
| chr7:2578767
|
C | T | 11 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.630+241C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2578767 | ||||||
| chr7:2578809
|
C | T | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.630+283C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2578809 | ||||||
| chr7:2578858
|
C | T | 102 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(99): Show | 103 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.630+332C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2578858 | ||||||
| chr7:2579000
|
G | A | 258 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(255): Show | 260 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.630+474G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579000 | ||||||
| chr7:2579006
|
T | C | 255 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(252): Show | 257 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.630+480T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579006 | ||||||
| chr7:2579023
|
C | T | 1 | a0001c0003t0027g0325 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.630+497C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579023 | ||||||
| chr7:2579041
|
C | CA | 9 | a0001c0001t0005g0329a0001c0001t0006g0391a0001c0001t0048g0242others(6): Show | 9 | HG00408.hp1 HG01175.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.630+531dupA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2579041 | |||||
| chr7:2579097
|
A | G | 2 | a0003c0005t0042g0369a0003c0005t0042g0378 | 2 | HG01981.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.630+571A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579097 | ||||||
| chr7:2579122
|
C | T | 4 | a0001c0010t0009g0005a0002c0015t0002g0075a0002c0015t0002g0076others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+596C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579122 | ||||||
| chr7:2579154
|
T | C | 3 | a0001c0003t0026g0234a0001c0003t0026g0365a0001c0003t0026g0386 | 3 | HG06807.hp1 NA20805.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.630+628T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579154 | ||||||
| chr7:2579274
|
G | C | 212 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(209): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.630+748G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579274 | ||||||
| chr7:2579291
|
G | A | 5 | a0008c0006t0023g0004a0008c0006t0023g0107a0008c0006t0023g0146others(2): Show | 5 | HG01167.hp2 HG01243.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+765G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579291 | ||||||
| chr7:2579293
|
G | A | 1 | a0004c0008t0010g0022 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.630+767G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579293 | ||||||
| chr7:2579457
|
C | G | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.630+931C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579457 | ||||||
| chr7:2579479
|
A | G | 12 | a0001c0029t0051g0171a0004c0008t0010g0015a0004c0008t0010g0016others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.630+953A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579479 | ||||||
| chr7:2579502
|
C | G | 1 | a0004c0008t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.630+976C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579502 | ||||||
| chr7:2579633
|
T | C | 3 | a0001c0003t0004g0174a0013c0024t0001g0201a0013c0024t0001g0203 | 3 | HG00738.hp2 HG01123.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.630+1107T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579633 | ||||||
| chr7:2579700
|
G | GGT | 10 | a0001c0003t0001g0324a0001c0011t0001g0413a0002c0002t0002g0156others(7): Show | 10 | HG01981.hp2 HG02080.hp1 HG03669.hp1 others(7): Show |
intron_variant | MODIFIER | c.630+1211_630+1212d others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2579700 | |||||
| chr7:2579700
|
GGT | G | 143 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.630+1211_630+1212d others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2579700 | |||||
| chr7:2579700
|
GGTGT | G | 11 | a0001c0003t0004g0098a0001c0003t0004g0174a0001c0003t0036g0245others(8): Show | 11 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.630+1209_630+1212d others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2579700 | |||||
| chr7:2579700
|
GGTGTGTG others(1): Show |
G | 4 | a0001c0001t0001g0343a0001c0001t0005g0166a0001c0001t0005g0178others(1): Show | 4 | HG01074.hp1 HG01081.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+1205_630+1212d others(10): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2579700 | |||||
| chr7:2579711
|
G | GTC | 9 | a0001c0029t0051g0171a0004c0008t0010g0015a0004c0008t0010g0016others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.630+1186_630+1187i others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2579711 | |||||
| chr7:2579729
|
G | C | 133 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(130): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.630+1203G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579729 | ||||||
| chr7:2579729
|
G | GTC | 10 | a0001c0003t0030g0155a0002c0015t0002g0075a0002c0015t0002g0076others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.630+1204_630+1205i others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2579729 | |||||
| chr7:2579729
|
G | GTGTC | 66 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(63): Show | 66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.630+1206_630+1207i others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2579729 | |||||
| chr7:2579729
|
G | GTGTGTC | 56 | a0001c0001t0001g0210a0001c0001t0001g0222a0001c0001t0004g0047others(53): Show | 57 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.630+1208_630+1209i others(8): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2579729 | |||||
| chr7:2579729
|
G | GTGTGTGT others(1): Show |
3 | a0001c0001t0001g0205a0001c0001t0004g0183a0002c0004t0003g0257 | 3 | HG01255.hp2 NA18946.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.630+1210_630+1211i others(10): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2579729 | |||||
| chr7:2579782
|
T | C | 27 | a0001c0019t0004g0093a0001c0019t0004g0105a0004c0008t0010g0015others(24): Show | 27 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.630+1256T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579782 | ||||||
| chr7:2579795
|
G | A | 2 | a0014c0018t0034g0114a0014c0018t0034g0115 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.630+1269G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579795 | ||||||
| chr7:2579812
|
T | G | 1 | a0001c0003t0001g0324 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.630+1286T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579812 | ||||||
| chr7:2579836
|
C | G | 255 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(252): Show | 257 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.630+1310C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579836 | ||||||
| chr7:2579840
|
A | C | 1 | a0002c0049t0073g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.630+1314A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579840 | ||||||
| chr7:2579849
|
TTA | T | 5 | a0007c0012t0019g0120a0007c0012t0019g0138a0007c0012t0019g0139others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+1324_630+1325d others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579849 | ||||||
| chr7:2579850
|
T | C | 263 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(260): Show | 265 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.630+1324T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579850 | ||||||
| chr7:2579852
|
G | C | 5 | a0007c0012t0019g0120a0007c0012t0019g0138a0007c0012t0019g0139others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+1326G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579852 | ||||||
| chr7:2579883
|
C | CACTACAG others(3): Show |
1 | a0002c0002t0003g0394 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.630+1357_630+1358i others(12): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579883 | ||||||
| chr7:2579886
|
G | T | 1 | a0002c0002t0003g0394 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.630+1360G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579886 | ||||||
| chr7:2579887
|
G | GACTACAG others(9): Show |
76 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0029others(73): Show | 76 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.630+1364_630+1379d others(18): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2579887 | |||||
| chr7:2579915
|
C | A | 1 | a0003c0005t0041g0337 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.630+1389C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2579915 | ||||||
| chr7:2580093
|
T | C | 3 | a0006c0009t0014g0267a0006c0009t0014g0303a0006c0009t0117g0091 | 3 | HG01081.hp1 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.630+1567T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580093 | ||||||
| chr7:2580130
|
C | T | 1 | a0001c0001t0016g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.630+1604C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580130 | ||||||
| chr7:2580137
|
G | A | 4 | a0007c0016t0035g0143a0007c0016t0050g0266a0007c0016t0079g0145others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+1611G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580137 | ||||||
| chr7:2580142
|
C | T | 1 | a0002c0002t0013g0351 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.630+1616C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580142 | ||||||
| chr7:2580286
|
G | A | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.630+1760G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580286 | ||||||
| chr7:2580293
|
C | CA | 102 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(99): Show | 103 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.630+1782dupA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2580293 | |||||
| chr7:2580293
|
CA | C | 18 | a0002c0002t0002g0069a0002c0049t0073g0054a0007c0016t0035g0143others(15): Show | 18 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.630+1782delA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2580293 | |||||
| chr7:2580295
|
A | C | 1 | a0002c0002t0003g0361 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.630+1769A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580295 | ||||||
| chr7:2580330
|
C | T | 4 | a0001c0010t0009g0005a0002c0015t0002g0075a0002c0015t0002g0076others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+1804C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580330 | ||||||
| chr7:2580405
|
T | A | 8 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(5): Show | 8 | HG01099.hp2 HG01255.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.630+1879T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580405 | ||||||
| chr7:2580411
|
A | C | 2 | a0004c0008t0010g0022a0004c0008t0010g0052 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.630+1885A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580411 | ||||||
| chr7:2580421
|
C | G | 2 | a0001c0001t0006g0332a0001c0001t0038g0328 | 2 | HG02015.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.630+1895C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580421 | ||||||
| chr7:2580435
|
C | T | 11 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.630+1909C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580435 | ||||||
| chr7:2580522
|
G | C | 5 | a0001c0003t0020g0021a0001c0003t0020g0118a0001c0003t0020g0119others(2): Show | 5 | HG02258.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+1996G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580522 | ||||||
| chr7:2580642
|
C | T | 1 | a0002c0002t0003g0361 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.631-1938C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580642 | ||||||
| chr7:2580688
|
C | G | 3 | a0001c0003t0001g0312a0001c0003t0001g0334a0001c0003t0001g0335 | 3 | NA18962.hp2 NA19007.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.631-1892C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580688 | ||||||
| chr7:2580709
|
A | G | 210 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(207): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.631-1871A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580709 | ||||||
| chr7:2580720
|
G | A | 1 | a0003c0005t0112g0373 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.631-1860G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580720 | ||||||
| chr7:2580902
|
T | G | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.631-1678T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2580902 | ||||||
| chr7:2581034
|
G | A | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.631-1546G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581034 | ||||||
| chr7:2581045
|
G | A | 8 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(5): Show | 8 | HG01099.hp2 HG01255.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.631-1535G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581045 | ||||||
| chr7:2581046
|
T | C | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.631-1534T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581046 | ||||||
| chr7:2581057
|
A | G | 5 | a0007c0012t0019g0120a0007c0012t0019g0138a0007c0012t0019g0139others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.631-1523A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581057 | ||||||
| chr7:2581255
|
C | G | 268 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(265): Show | 270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.631-1325C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581255 | ||||||
| chr7:2581299
|
A | G | 1 | a0002c0002t0003g0360 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.631-1281A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581299 | ||||||
| chr7:2581341
|
G | C | 1 | a0001c0001t0004g0047 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.631-1239G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581341 | ||||||
| chr7:2581366
|
C | T | 4 | a0001c0010t0009g0005a0002c0015t0002g0075a0002c0015t0002g0076others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-1214C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581366 | ||||||
| chr7:2581445
|
A | G | 4 | a0001c0010t0009g0005a0002c0015t0002g0075a0002c0015t0002g0076others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-1135A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581445 | ||||||
| chr7:2581539
|
A | G | 91 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.631-1041A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581539 | ||||||
| chr7:2581539
|
A | T | 1 | a0003c0025t0043g0339 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.631-1041A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581539 | ||||||
| chr7:2581710
|
T | TC | 3 | a0001c0001t0004g0183a0001c0001t0016g0204a0002c0004t0012g0294 | 3 | HG01952.hp2 NA18946.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.631-869dupC | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2581710 | |||||
| chr7:2581711
|
C | CCT | 96 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(93): Show | 97 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.631-869_631-868ins others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581711 | ||||||
| chr7:2581711
|
C | CT | 33 | a0001c0010t0009g0005a0001c0019t0004g0093a0001c0019t0004g0105others(30): Show | 33 | HG00280.hp2 HG00544.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.631-853dupT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2581711 | |||||
| chr7:2581711
|
CT | C | 14 | a0001c0010t0009g0121a0001c0010t0009g0122a0001c0010t0009g0124others(11): Show | 14 | HG00639.hp2 HG01192.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.631-853delT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2581711 | |||||
| chr7:2581716
|
T | G | 12 | a0008c0006t0023g0004a0008c0006t0023g0107a0008c0006t0023g0146others(9): Show | 12 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.631-864T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581716 | ||||||
| chr7:2581732
|
T | C | 268 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(265): Show | 270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.631-848T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581732 | ||||||
| chr7:2581733
|
G | T | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.631-847G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581733 | ||||||
| chr7:2581741
|
G | A | 108 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(105): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.631-839G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581741 | ||||||
| chr7:2581754
|
C | G | 210 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(207): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.631-826C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581754 | ||||||
| chr7:2581819
|
C | T | 6 | a0001c0029t0051g0171a0002c0049t0073g0054a0007c0016t0035g0143others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-761C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581819 | ||||||
| chr7:2581841
|
C | G | 1 | a0001c0001t0006g0391 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.631-739C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581841 | ||||||
| chr7:2581859
|
G | A | 1 | a0001c0001t0094g0409 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.631-721G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581859 | ||||||
| chr7:2581864
|
C | T | 209 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(206): Show | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.631-716C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581864 | ||||||
| chr7:2581865
|
G | A | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.631-715G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581865 | ||||||
| chr7:2581891
|
T | A | 7 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0006g0233others(4): Show | 7 | HG00140.hp2 HG00280.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.631-689T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581891 | ||||||
| chr7:2581902
|
C | T | 4 | a0001c0010t0009g0005a0002c0015t0002g0075a0002c0015t0002g0076others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-678C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581902 | ||||||
| chr7:2581905
|
G | A | 1 | a0001c0001t0056g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.631-675G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581905 | ||||||
| chr7:2581933
|
T | C | 254 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(251): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.631-647T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581933 | ||||||
| chr7:2581966
|
C | T | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-614C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581966 | ||||||
| chr7:2581998
|
C | T | 1 | a0001c0001t0017g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.631-582C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2581998 | ||||||
| chr7:2582069
|
GA | G | 3 | a0002c0002t0002g0069a0002c0002t0002g0070a0016c0046t0002g0056 | 3 | HG01975.hp2 HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.631-507delA | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 2582069 | |||||
| chr7:2582088
|
C | T | 9 | a0001c0010t0009g0121a0001c0010t0009g0122a0001c0010t0009g0124others(6): Show | 9 | HG00639.hp2 HG01192.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.631-492C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582088 | ||||||
| chr7:2582097
|
T | C | 6 | a0001c0001t0005g0028a0001c0001t0005g0041a0003c0005t0110g0258others(3): Show | 6 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-483T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582097 | ||||||
| chr7:2582108
|
C | A | 2 | a0004c0008t0064g0197a0004c0008t0070g0198 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.631-472C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582108 | ||||||
| chr7:2582131
|
C | T | 1 | a0001c0001t0005g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.631-449C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582131 | ||||||
| chr7:2582149
|
C | A | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.631-431C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582149 | ||||||
| chr7:2582151
|
C | T | 1 | a0006c0044t0033g0085 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.631-429C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582151 | ||||||
| chr7:2582153
|
G | T | 1 | a0001c0001t0005g0094 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.631-427G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582153 | ||||||
| chr7:2582277
|
C | T | 2 | a0002c0004t0002g0008a0002c0004t0002g0009 | 2 | NA18964.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.631-303C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582277 | ||||||
| chr7:2582289
|
C | G | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.631-291C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582289 | ||||||
| chr7:2582304
|
G | C | 1 | a0001c0001t0006g0255 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.631-276G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582304 | ||||||
| chr7:2582307
|
T | C | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.631-273T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582307 | ||||||
| chr7:2582356
|
C | T | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.631-224C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582356 | ||||||
| chr7:2582366
|
C | T | 101 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(98): Show | 102 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.631-214C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582366 | ||||||
| chr7:2582367
|
G | A | 8 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(5): Show | 8 | HG01496.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.631-213G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582367 | ||||||
| chr7:2582373
|
G | A | 1 | a0002c0002t0002g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.631-207G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582373 | ||||||
| chr7:2582392
|
A | T | 3 | a0002c0002t0002g0133a0002c0002t0002g0153a0002c0002t0002g0158 | 3 | NA18968.hp2 NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.631-188A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582392 | ||||||
| chr7:2582393
|
G | GTC | 3 | a0002c0002t0002g0133a0002c0002t0002g0153a0002c0002t0002g0158 | 3 | NA18968.hp2 NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.631-187_631-186ins others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582393 | ||||||
| chr7:2582445
|
C | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0222 | 2 | NA19009.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.631-135C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582445 | ||||||
| chr7:2582467
|
C | T | 102 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(99): Show | 103 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.631-113C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582467 | ||||||
| chr7:2582478
|
G | T | 1 | a0001c0003t0096g0407 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.631-102G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582478 | ||||||
| chr7:2582499
|
G | A | 39 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(36): Show | 39 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.631-81G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582499 | ||||||
| chr7:2582546
|
C | T | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.631-34C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582546 | ||||||
| chr7:2582570
|
C | T | 3 | a0002c0002t0002g0069a0002c0002t0002g0070a0016c0046t0002g0056 | 3 | HG01975.hp2 HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.631-10C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 8/21 | chr7 | 2582570 | ||||||
| chr7:2582691
|
G | A | 13 | a0001c0003t0026g0234a0001c0003t0026g0365a0001c0003t0026g0386others(10): Show | 13 | HG01496.hp2 HG02717.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.701+41G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2582691 | ||||||
| chr7:2582802
|
A | C | 10 | a0001c0010t0009g0005a0001c0010t0009g0121a0001c0010t0009g0122others(7): Show | 10 | HG00639.hp2 HG01192.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.701+152A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2582802 | ||||||
| chr7:2582835
|
A | G | 6 | a0001c0010t0009g0121a0001c0010t0009g0122a0001c0010t0009g0124others(3): Show | 6 | HG01192.hp2 HG02486.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.701+185A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2582835 | ||||||
| chr7:2582869
|
G | A | 2 | a0002c0002t0015g0321a0002c0002t0015g0359 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.701+219G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2582869 | ||||||
| chr7:2582933
|
C | T | 1 | a0002c0002t0076g0065 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.701+283C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2582933 | ||||||
| chr7:2582938
|
T | C | 210 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(207): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.701+288T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2582938 | ||||||
| chr7:2582975
|
G | T | 268 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(265): Show | 270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.701+325G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2582975 | ||||||
| chr7:2583015
|
T | C | 268 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(265): Show | 270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.701+365T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583015 | ||||||
| chr7:2583054
|
C | A | 2 | a0001c0001t0031g0142a0001c0001t0055g0170 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.701+404C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583054 | ||||||
| chr7:2583095
|
C | T | 1 | a0002c0004t0003g0213 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.701+445C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583095 | ||||||
| chr7:2583150
|
C | G | 12 | a0008c0006t0023g0004a0008c0006t0023g0107a0008c0006t0023g0146others(9): Show | 12 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.702-487C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583150 | ||||||
| chr7:2583163
|
A | C | 1 | a0001c0003t0001g0313 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.702-474A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583163 | ||||||
| chr7:2583221
|
G | T | 1 | a0005c0007t0007g0275 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.702-416G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583221 | ||||||
| chr7:2583290
|
G | A | 7 | a0001c0029t0051g0171a0004c0008t0010g0015a0004c0008t0010g0016others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.702-347G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583290 | ||||||
| chr7:2583321
|
C | T | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702-316C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583321 | ||||||
| chr7:2583401
|
A | T | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.702-236A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583401 | ||||||
| chr7:2583405
|
T | C | 210 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(207): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.702-232T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583405 | ||||||
| chr7:2583453
|
C | T | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.702-184C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583453 | ||||||
| chr7:2583491
|
A | T | 4 | a0001c0010t0009g0005a0002c0015t0002g0075a0002c0015t0002g0076others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.702-146A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583491 | ||||||
| chr7:2583525
|
T | C | 12 | a0008c0006t0023g0004a0008c0006t0023g0107a0008c0006t0023g0146others(9): Show | 12 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.702-112T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583525 | ||||||
| chr7:2583526
|
G | C | 5 | a0008c0006t0023g0004a0008c0006t0023g0107a0008c0006t0023g0146others(2): Show | 5 | HG01167.hp2 HG01243.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.702-111G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583526 | ||||||
| chr7:2583557
|
C | A | 4 | a0001c0010t0009g0005a0002c0015t0002g0075a0002c0015t0002g0076others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.702-80C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583557 | ||||||
| chr7:2583557
|
C | T | 11 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.702-80C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 9/21 | chr7 | 2583557 | ||||||
| chr7:2583717
|
G | A | 108 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(105): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): Show |
splice_region_variant&intron_variant | LOW | c.774+8G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583717 | ||||||
| chr7:2583719
|
G | A | 5 | a0007c0012t0019g0120a0007c0012t0019g0138a0007c0012t0019g0139others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+10G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583719 | ||||||
| chr7:2583722
|
GGGCGGCG others(23): Show |
G | 1 | a0001c0001t0048g0242 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.774+16_774+45delCG others(28): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr7 | 2583722 | |||||
| chr7:2583725
|
C | T | 3 | a0003c0005t0110g0258a0003c0005t0113g0283a0003c0005t0114g0251 | 3 | HG00099.hp2 HG01934.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.774+16C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583725 | ||||||
| chr7:2583728
|
C | T | 2 | a0002c0004t0003g0223a0002c0004t0003g0238 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.774+19C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583728 | ||||||
| chr7:2583762
|
G | A | 1 | a0001c0001t0048g0242 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.774+53G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583762 | ||||||
| chr7:2583767
|
AGGGCGGG others(134): Show |
A | 1 | a0001c0001t0001g0411 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.774+89_774+229del | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr7 | 2583767 | |||||
| chr7:2583780
|
AGCTGGGC others(24): Show |
A | 101 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(98): Show | 102 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.774+89_774+119delA others(30): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr7 | 2583780 | |||||
| chr7:2583802
|
C | T | 1 | a0007c0037t0035g0014 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.774+93C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583802 | ||||||
| chr7:2583809
|
C | T | 1 | a0001c0001t0097g0286 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.774+100C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583809 | ||||||
| chr7:2583811
|
T | A | 6 | a0001c0001t0048g0242a0008c0006t0024g0151a0008c0006t0046g0111others(3): Show | 6 | HG01192.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+102T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583811 | ||||||
| chr7:2583818
|
C | T | 4 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(1): Show | 4 | HG01496.hp2 HG02922.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+109C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583818 | ||||||
| chr7:2583822
|
G | GGGGCGGA | 5 | a0008c0006t0024g0151a0008c0006t0046g0111a0008c0006t0086g0125others(2): Show | 5 | HG01192.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+119_774+120ins others(7): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr7 | 2583822 | |||||
| chr7:2583828
|
GGCACCGA others(72): Show |
G | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.774+121_774+199del others(79): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr7 | 2583828 | |||||
| chr7:2583835
|
A | T | 12 | a0002c0002t0002g0126a0002c0002t0002g0134a0002c0002t0002g0141others(9): Show | 12 | HG01192.hp1 HG02572.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.774+126A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583835 | ||||||
| chr7:2583842
|
C | T | 41 | a0002c0004t0002g0001a0002c0004t0002g0007a0002c0004t0002g0008others(38): Show | 42 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.774+133C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583842 | ||||||
| chr7:2583846
|
GGGGCGGA | G | 6 | a0003c0005t0088g0164a0008c0006t0024g0151a0008c0006t0046g0111others(3): Show | 6 | HG01192.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+144_774+150del others(7): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr7 | 2583846 | |||||
| chr7:2583866
|
T | A | 6 | a0003c0005t0088g0164a0008c0006t0024g0151a0008c0006t0046g0111others(3): Show | 6 | HG01192.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+157T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583866 | ||||||
| chr7:2583866
|
TGCTGGGT others(48): Show |
T | 4 | a0001c0010t0009g0005a0002c0015t0002g0075a0002c0015t0002g0076others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+164_774+218del others(55): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr7 | 2583866 | |||||
| chr7:2583873
|
T | C | 6 | a0003c0005t0088g0164a0008c0006t0024g0151a0008c0006t0046g0111others(3): Show | 6 | HG01192.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+164T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583873 | ||||||
| chr7:2583873
|
TGGCGGGG others(72): Show |
T | 5 | a0001c0003t0001g0227a0001c0003t0001g0229a0001c0003t0001g0239others(2): Show | 5 | HG04204.hp1 NA18959.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+195_775-254del others(79): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr7 | 2583873 | |||||
| chr7:2583884
|
AGGGCGGG others(17): Show |
A | 8 | a0001c0003t0001g0260a0001c0003t0001g0313a0001c0003t0004g0098others(5): Show | 8 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.774+188_774+211del others(24): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr7 | 2583884 | |||||
| chr7:2583897
|
TGCTGGGC others(17): Show |
T | 242 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(239): Show | 244 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.774+230_774+253del others(24): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr7 | 2583897 | |||||
| chr7:2583904
|
C | T | 6 | a0003c0005t0088g0164a0008c0006t0024g0151a0008c0006t0046g0111others(3): Show | 6 | HG01192.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+195C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583904 | ||||||
| chr7:2583908
|
G | A | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.774+199G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583908 | ||||||
| chr7:2583908
|
G | GGGGCGGA | 6 | a0003c0005t0088g0164a0008c0006t0024g0151a0008c0006t0046g0111others(3): Show | 6 | HG01192.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+205_774+206ins others(7): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr7 | 2583908 | |||||
| chr7:2583921
|
A | T | 9 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(6): Show | 9 | HG01192.hp1 HG01496.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.774+212A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583921 | ||||||
| chr7:2583928
|
CGGCGGGG others(48): Show |
C | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+230_775-243del others(55): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr7 | 2583928 | |||||
| chr7:2583931
|
C | T | 1 | a0007c0016t0079g0145 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.774+222C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583931 | ||||||
| chr7:2583943
|
C | T | 9 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(6): Show | 9 | HG01496.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.774+234C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583943 | ||||||
| chr7:2583968
|
G | A | 2 | a0001c0001t0006g0391a0002c0049t0073g0054 | 2 | NA19030.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.774+259G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2583968 | ||||||
| chr7:2584033
|
G | T | 1 | a0002c0002t0003g0360 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.775-203G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2584033 | ||||||
| chr7:2584064
|
C | A | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-172C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2584064 | ||||||
| chr7:2584094
|
C | T | 6 | a0001c0010t0009g0121a0001c0010t0009g0122a0001c0010t0009g0124others(3): Show | 6 | HG01192.hp2 HG02486.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-142C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2584094 | ||||||
| chr7:2584097
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.775-139A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2584097 | ||||||
| chr7:2584100
|
G | C | 1 | a0002c0002t0002g0184 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.775-136G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2584100 | ||||||
| chr7:2584114
|
C | T | 11 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.775-122C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2584114 | ||||||
| chr7:2584139
|
C | T | 5 | a0002c0002t0002g0073a0002c0002t0002g0087a0002c0004t0072g0162others(2): Show | 5 | HG02293.hp2 HG02300.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-97C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2584139 | ||||||
| chr7:2584167
|
G | T | 92 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(89): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.775-69G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 10/21 | chr7 | 2584167 | ||||||
| chr7:2584297
|
G | A | 1 | a0002c0004t0003g0295 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.824+12G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2584297 | ||||||
| chr7:2584330
|
G | A | 1 | a0026c0032t0021g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.824+45G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2584330 | ||||||
| chr7:2584373
|
C | T | 4 | a0007c0016t0035g0143a0007c0016t0050g0266a0007c0016t0079g0145others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.824+88C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2584373 | ||||||
| chr7:2584379
|
A | G | 1 | a0005c0007t0007g0278 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.824+94A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2584379 | ||||||
| chr7:2584385
|
C | G | 2 | a0004c0008t0064g0197a0004c0008t0070g0198 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.824+100C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2584385 | ||||||
| chr7:2584430
|
G | C | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.824+145G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2584430 | ||||||
| chr7:2584514
|
C | T | 1 | a0009c0013t0022g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.824+229C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2584514 | ||||||
| chr7:2584766
|
G | A | 2 | a0002c0002t0002g0010a0002c0045t0029g0080 | 2 | HG01106.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.824+481G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2584766 | ||||||
| chr7:2584778
|
T | C | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.824+493T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2584778 | ||||||
| chr7:2584794
|
C | T | 209 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(206): Show | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.824+509C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2584794 | ||||||
| chr7:2584857
|
T | G | 1 | a0002c0015t0002g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.824+572T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2584857 | ||||||
| chr7:2584971
|
A | C | 3 | a0002c0002t0002g0053a0002c0002t0003g0319a0002c0002t0003g0362 | 3 | HG00544.hp1 HG00558.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.824+686A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2584971 | ||||||
| chr7:2585019
|
C | T | 2 | a0001c0001t0031g0142a0001c0001t0055g0170 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.824+734C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585019 | ||||||
| chr7:2585030
|
C | G | 1 | a0001c0001t0052g0060 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.824+745C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585030 | ||||||
| chr7:2585048
|
A | AT | 111 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(108): Show | 112 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.824+779dupT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr7 | 2585048 | |||||
| chr7:2585048
|
A | ATT | 94 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(91): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.824+778_824+779dup others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr7 | 2585048 | |||||
| chr7:2585048
|
A | ATTT | 8 | a0001c0001t0057g0327a0003c0005t0025g0167a0008c0006t0086g0125others(5): Show | 8 | HG01069.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.824+777_824+779dup others(3): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr7 | 2585048 | |||||
| chr7:2585048
|
AT | A | 6 | a0001c0003t0001g0229a0001c0003t0001g0389a0001c0003t0026g0386others(3): Show | 6 | HG06807.hp1 NA18959.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.824+779delT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr7 | 2585048 | |||||
| chr7:2585091
|
G | A | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.824+806G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585091 | ||||||
| chr7:2585135
|
A | G | 1 | a0001c0001t0052g0060 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.824+850A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585135 | ||||||
| chr7:2585185
|
A | G | 2 | a0003c0005t0041g0330a0003c0005t0041g0337 | 2 | HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.824+900A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585185 | ||||||
| chr7:2585197
|
C | A | 9 | a0001c0010t0009g0121a0001c0010t0009g0122a0001c0010t0009g0124others(6): Show | 9 | HG00639.hp2 HG01192.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.824+912C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585197 | ||||||
| chr7:2585228
|
G | A | 15 | a0001c0019t0004g0093a0001c0019t0004g0105a0005c0007t0007g0002others(12): Show | 15 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.824+943G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585228 | ||||||
| chr7:2585280
|
C | T | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.825-928C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585280 | ||||||
| chr7:2585299
|
A | G | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.825-909A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585299 | ||||||
| chr7:2585383
|
CAT | C | 6 | a0001c0001t0017g0140a0001c0001t0017g0144a0001c0001t0021g0129others(3): Show | 6 | HG02280.hp2 HG02717.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.825-824_825-823del others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585383 | ||||||
| chr7:2585388
|
G | A | 1 | a0002c0004t0013g0256 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.825-820G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585388 | ||||||
| chr7:2585445
|
C | G | 3 | a0002c0015t0002g0075a0002c0015t0002g0076a0002c0015t0002g0097 | 3 | HG02055.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.825-763C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585445 | ||||||
| chr7:2585477
|
G | A | 16 | a0008c0006t0023g0004a0008c0006t0023g0107a0008c0006t0023g0146others(13): Show | 16 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.825-731G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585477 | ||||||
| chr7:2585671
|
C | A | 1 | a0001c0001t0001g0284 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.825-537C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585671 | ||||||
| chr7:2585747
|
C | A | 1 | a0015c0031t0103g0296 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.825-461C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585747 | ||||||
| chr7:2585748
|
A | C | 1 | a0015c0031t0103g0296 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.825-460A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585748 | ||||||
| chr7:2585749
|
C | A | 1 | a0015c0031t0103g0296 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.825-459C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585749 | ||||||
| chr7:2585774
|
C | G | 268 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(265): Show | 270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.825-434C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585774 | ||||||
| chr7:2585796
|
A | G | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.825-412A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585796 | ||||||
| chr7:2585892
|
A | G | 268 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(265): Show | 270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.825-316A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585892 | ||||||
| chr7:2585940
|
A | C | 1 | a0002c0004t0077g0104 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.825-268A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585940 | ||||||
| chr7:2585940
|
A | G | 1 | a0001c0001t0052g0060 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.825-268A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585940 | ||||||
| chr7:2585955
|
C | T | 1 | a0002c0002t0002g0133 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.825-253C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585955 | ||||||
| chr7:2585998
|
A | G | 11 | a0002c0002t0003g0293a0002c0002t0003g0322a0002c0002t0003g0349others(8): Show | 11 | NA18747.hp1 NA18944.hp1 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.825-210A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2585998 | ||||||
| chr7:2586006
|
G | T | 3 | a0002c0015t0002g0075a0002c0015t0002g0076a0002c0015t0002g0097 | 3 | HG02055.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.825-202G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2586006 | ||||||
| chr7:2586023
|
GC | G | 210 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(207): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.825-184delC | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2586023 | ||||||
| chr7:2586035
|
C | A | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.825-173C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2586035 | ||||||
| chr7:2586050
|
A | G | 1 | a0001c0047t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.825-158A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2586050 | ||||||
| chr7:2586051
|
A | C | 2 | a0001c0029t0051g0171a0002c0049t0073g0054 | 2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.825-157A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2586051 | ||||||
| chr7:2586076
|
A | G | 1 | a0001c0001t0001g0343 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.825-132A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2586076 | ||||||
| chr7:2586204
|
C | T | 102 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(99): Show | 103 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(100): Show |
splice_region_variant&intron_variant | LOW | c.825-4C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 11/21 | chr7 | 2586204 | ||||||
| chr7:2586404
|
CCAGGGAA others(3): Show |
C | 268 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(265): Show | 270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.988+49_988+58delAA others(8): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr7 | 2586404 | |||||
| chr7:2586426
|
AGGGCATG others(6): Show |
A | 1 | a0002c0002t0002g0053 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.988+59_988+71delCA others(11): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr7 | 2586426 | |||||
| chr7:2586477
|
A | G | 2 | a0002c0002t0002g0029a0002c0002t0002g0049 | 2 | NA18961.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.988+106A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2586477 | ||||||
| chr7:2586503
|
C | T | 1 | a0002c0002t0003g0353 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.988+132C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2586503 | ||||||
| chr7:2586586
|
G | T | 6 | a0001c0029t0051g0171a0002c0049t0073g0054a0007c0016t0035g0143others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.988+215G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2586586 | ||||||
| chr7:2586638
|
TCAGATGG others(7): Show |
T | 1 | a0015c0031t0103g0296 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.988+268_988+281del others(14): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2586638 | ||||||
| chr7:2586757
|
G | A | 1 | a0002c0015t0002g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.988+386G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2586757 | ||||||
| chr7:2586774
|
C | T | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.988+403C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2586774 | ||||||
| chr7:2586805
|
G | A | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.988+434G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2586805 | ||||||
| chr7:2586927
|
G | A | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.988+556G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2586927 | ||||||
| chr7:2586976
|
T | C | 257 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(254): Show | 259 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.988+605T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2586976 | ||||||
| chr7:2587017
|
G | A | 1 | a0002c0002t0002g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.988+646G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587017 | ||||||
| chr7:2587062
|
G | A | 15 | a0001c0029t0051g0171a0002c0015t0002g0075a0002c0015t0002g0076others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.988+691G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587062 | ||||||
| chr7:2587068
|
C | G | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.988+697C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587068 | ||||||
| chr7:2587190
|
A | G | 1 | a0001c0003t0096g0407 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.989-632A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587190 | ||||||
| chr7:2587224
|
T | G | 1 | a0002c0002t0003g0353 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.989-598T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587224 | ||||||
| chr7:2587237
|
C | T | 7 | a0001c0010t0009g0121a0001c0010t0009g0122a0001c0010t0009g0124others(4): Show | 7 | HG01192.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.989-585C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587237 | ||||||
| chr7:2587240
|
G | A | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.989-582G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587240 | ||||||
| chr7:2587257
|
G | T | 1 | a0002c0002t0003g0353 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.989-565G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587257 | ||||||
| chr7:2587262
|
G | C | 257 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(254): Show | 259 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.989-560G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587262 | ||||||
| chr7:2587277
|
C | T | 103 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(100): Show | 104 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.989-545C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587277 | ||||||
| chr7:2587410
|
G | A | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.989-412G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587410 | ||||||
| chr7:2587660
|
C | T | 45 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(42): Show | 45 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.989-162C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587660 | ||||||
| chr7:2587676
|
T | A | 268 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(265): Show | 270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.989-146T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 12/21 | chr7 | 2587676 | ||||||
| chr7:2587937
|
G | A | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1044+60G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2587937 | ||||||
| chr7:2587939
|
GC | G | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1044+63delC | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2587939 | ||||||
| chr7:2587944
|
CAG | C | 93 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(90): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1044+68_1044+69del others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2587944 | ||||||
| chr7:2587980
|
T | C | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1044+103T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2587980 | ||||||
| chr7:2588009
|
G | A | 4 | a0005c0007t0007g0002a0005c0007t0089g0077a0010c0017t0007g0002others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+132G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588009 | ||||||
| chr7:2588032
|
A | G | 1 | a0002c0002t0039g0209 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1044+155A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588032 | ||||||
| chr7:2588103
|
C | T | 3 | a0001c0047t0001g0308a0004c0028t0067g0020a0006c0048t0065g0165 | 3 | HG00639.hp2 HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1044+226C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588103 | ||||||
| chr7:2588105
|
C | T | 2 | a0004c0008t0064g0197a0004c0008t0070g0198 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1044+228C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588105 | ||||||
| chr7:2588268
|
A | G | 2 | a0002c0002t0003g0392a0002c0002t0003g0394 | 2 | NA18964.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1044+391A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588268 | ||||||
| chr7:2588283
|
C | T | 13 | a0001c0019t0004g0093a0001c0019t0004g0105a0005c0007t0007g0002others(10): Show | 13 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1044+406C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588283 | ||||||
| chr7:2588345
|
T | C | 6 | a0001c0029t0051g0171a0002c0049t0073g0054a0007c0016t0035g0143others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044+468T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588345 | ||||||
| chr7:2588358
|
T | G | 2 | a0001c0001t0005g0057a0001c0001t0005g0094 | 2 | HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1044+481T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588358 | ||||||
| chr7:2588363
|
C | T | 1 | a0002c0002t0003g0353 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1044+486C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588363 | ||||||
| chr7:2588364
|
T | C | 1 | a0002c0002t0003g0353 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1044+487T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588364 | ||||||
| chr7:2588376
|
A | G | 1 | a0001c0001t0005g0166 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1044+499A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588376 | ||||||
| chr7:2588429
|
C | T | 1 | a0002c0014t0003g0231 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1044+552C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588429 | ||||||
| chr7:2588446
|
C | T | 13 | a0003c0025t0085g0110a0008c0006t0023g0004a0008c0006t0023g0107others(10): Show | 13 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1044+569C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588446 | ||||||
| chr7:2588447
|
G | A | 1 | a0001c0003t0001g0239 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1044+570G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588447 | ||||||
| chr7:2588449
|
G | C | 28 | a0001c0019t0004g0093a0001c0019t0004g0105a0001c0029t0051g0171others(25): Show | 28 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1044+572G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588449 | ||||||
| chr7:2588515
|
G | A | 8 | a0001c0010t0009g0005a0001c0010t0009g0121a0001c0010t0009g0122others(5): Show | 8 | HG01192.hp2 HG01243.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1044+638G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588515 | ||||||
| chr7:2588543
|
C | T | 2 | a0003c0020t0083g0159a0003c0020t0084g0160 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1044+666C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588543 | ||||||
| chr7:2588581
|
C | T | 8 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(5): Show | 8 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1044+704C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588581 | ||||||
| chr7:2588588
|
C | T | 35 | a0001c0022t0090g0082a0001c0022t0091g0081a0001c0029t0051g0171others(32): Show | 35 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1044+711C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588588 | ||||||
| chr7:2588601
|
C | A | 1 | a0001c0003t0004g0098 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1044+724C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588601 | ||||||
| chr7:2588654
|
G | GT | 162 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0237others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1044+805dupT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr7 | 2588654 | |||||
| chr7:2588654
|
G | GTT | 37 | a0001c0001t0004g0047a0001c0001t0005g0095a0001c0001t0005g0323others(34): Show | 37 | HG00423.hp1 HG00741.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1044+804_1044+805d others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr7 | 2588654 | |||||
| chr7:2588654
|
G | GTTTTTTT | 7 | a0001c0010t0009g0005a0001c0010t0009g0121a0001c0010t0009g0122others(4): Show | 7 | HG01192.hp2 HG01243.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1044+799_1044+805d others(9): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr7 | 2588654 | |||||
| chr7:2588654
|
GT | G | 12 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(9): Show | 12 | HG01256.hp1 HG01346.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1044+805delT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr7 | 2588654 | |||||
| chr7:2588654
|
GTT | G | 15 | a0001c0019t0004g0093a0001c0019t0004g0105a0001c0022t0091g0081others(12): Show | 15 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.1044+804_1044+805d others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr7 | 2588654 | |||||
| chr7:2588654
|
GTTTTTTT others(4): Show |
G | 2 | a0001c0047t0001g0308a0006c0048t0065g0165 | 2 | HG00639.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1044+795_1044+805d others(13): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr7 | 2588654 | |||||
| chr7:2588713
|
G | A | 109 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(106): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1044+836G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588713 | ||||||
| chr7:2588940
|
C | T | 1 | a0001c0001t0004g0040 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1045-967C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588940 | ||||||
| chr7:2588960
|
T | C | 216 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(213): Show | 218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1045-947T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588960 | ||||||
| chr7:2588965
|
T | C | 1 | a0002c0002t0076g0065 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1045-942T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2588965 | ||||||
| chr7:2589017
|
G | T | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1045-890G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589017 | ||||||
| chr7:2589018
|
C | T | 3 | a0001c0022t0090g0082a0001c0022t0091g0081a0007c0039t0092g0013 | 3 | HG02451.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1045-889C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589018 | ||||||
| chr7:2589055
|
A | G | 1 | a0001c0003t0016g0311 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1045-852A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589055 | ||||||
| chr7:2589079
|
G | A | 94 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(91): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1045-828G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589079 | ||||||
| chr7:2589173
|
G | T | 1 | a0001c0001t0001g0222 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1045-734G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589173 | ||||||
| chr7:2589200
|
T | G | 1 | a0001c0003t0004g0071 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1045-707T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589200 | ||||||
| chr7:2589318
|
T | TGATTGCA others(11): Show |
1 | a0024c0042t0074g0059 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1045-587_1045-570d others(20): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr7 | 2589318 | |||||
| chr7:2589386
|
A | C | 108 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(105): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1045-521A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589386 | ||||||
| chr7:2589394
|
G | A | 1 | a0001c0019t0004g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1045-513G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589394 | ||||||
| chr7:2589409
|
A | G | 15 | a0001c0029t0051g0171a0002c0015t0002g0075a0002c0015t0002g0076others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1045-498A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589409 | ||||||
| chr7:2589461
|
G | T | 12 | a0008c0006t0023g0004a0008c0006t0023g0107a0008c0006t0023g0146others(9): Show | 12 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1045-446G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589461 | ||||||
| chr7:2589574
|
C | T | 1 | a0002c0002t0003g0392 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1045-333C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589574 | ||||||
| chr7:2589615
|
T | C | 1 | a0001c0003t0096g0407 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1045-292T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589615 | ||||||
| chr7:2589632
|
G | A | 2 | a0002c0004t0003g0223a0002c0004t0003g0238 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1045-275G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589632 | ||||||
| chr7:2589666
|
C | T | 1 | a0009c0013t0022g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1045-241C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589666 | ||||||
| chr7:2589673
|
G | T | 1 | a0001c0001t0005g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1045-234G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589673 | ||||||
| chr7:2589724
|
G | A | 15 | a0001c0029t0051g0171a0002c0015t0002g0075a0002c0015t0002g0076others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1045-183G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589724 | ||||||
| chr7:2589740
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1045-167G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 13/21 | chr7 | 2589740 | ||||||
| chr7:2590119
|
A | C | 1 | a0002c0002t0002g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1244+13A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590119 | ||||||
| chr7:2590126
|
C | T | 2 | a0003c0005t0088g0164a0027c0052t0001g0344 | 2 | HG04199.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1244+20C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590126 | ||||||
| chr7:2590141
|
G | A | 1 | a0002c0002t0002g0044 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1244+35G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590141 | ||||||
| chr7:2590141
|
G | GGGCACAG others(49): Show |
1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1244+117_1244+172d others(58): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr7 | 2590141 | |||||
| chr7:2590231
|
C | CAGGCCCC others(49): Show |
5 | a0007c0012t0019g0120a0007c0012t0019g0138a0007c0012t0019g0139others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1244+172_1244+173i others(58): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr7 | 2590231 | |||||
| chr7:2590231
|
C | CAGGCCCC others(49): Show |
334 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(331): Show | 336 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1244+172_1244+173i others(58): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr7 | 2590231 | |||||
| chr7:2590231
|
C | CAGGCCCC others(49): Show |
19 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(16): Show | 19 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.1244+165_1244+166i others(58): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr7 | 2590231 | |||||
| chr7:2590231
|
C | G | 5 | a0001c0001t0116g0263a0002c0002t0002g0044a0002c0002t0105g0317others(2): Show | 5 | HG02132.hp1 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1244+125C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590231 | ||||||
| chr7:2590282
|
C | T | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1244+176C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590282 | ||||||
| chr7:2590297
|
C | A | 106 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1244+191C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590297 | ||||||
| chr7:2590342
|
A | T | 2 | a0011c0021t0040g0370a0011c0021t0040g0374 | 2 | HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1244+236A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590342 | ||||||
| chr7:2590362
|
A | G | 212 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(209): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1244+256A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590362 | ||||||
| chr7:2590418
|
A | G | 209 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(206): Show | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1244+312A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590418 | ||||||
| chr7:2590461
|
G | T | 3 | a0002c0015t0002g0075a0002c0015t0002g0076a0002c0015t0002g0097 | 3 | HG02055.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1244+355G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590461 | ||||||
| chr7:2590492
|
C | T | 1 | a0001c0001t0006g0388 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1244+386C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590492 | ||||||
| chr7:2590500
|
C | T | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1244+394C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590500 | ||||||
| chr7:2590527
|
G | A | 1 | a0001c0001t0005g0408 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1244+421G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590527 | ||||||
| chr7:2590705
|
C | T | 1 | a0002c0004t0003g0213 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1244+599C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590705 | ||||||
| chr7:2590821
|
A | C | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1244+715A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590821 | ||||||
| chr7:2590883
|
C | T | 1 | a0006c0009t0102g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1244+777C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590883 | ||||||
| chr7:2590895
|
G | T | 12 | a0008c0006t0023g0004a0008c0006t0023g0107a0008c0006t0023g0146others(9): Show | 12 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1244+789G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2590895 | ||||||
| chr7:2591081
|
C | T | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1244+975C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591081 | ||||||
| chr7:2591185
|
C | T | 8 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(5): Show | 8 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244+1079C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591185 | ||||||
| chr7:2591187
|
A | G | 1 | a0002c0002t0003g0298 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1244+1081A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591187 | ||||||
| chr7:2591202
|
A | G | 11 | a0002c0002t0003g0293a0002c0002t0003g0322a0002c0002t0003g0349others(8): Show | 11 | NA18747.hp1 NA18944.hp1 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.1244+1096A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591202 | ||||||
| chr7:2591263
|
C | G | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1244+1157C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591263 | ||||||
| chr7:2591267
|
G | A | 265 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(262): Show | 267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1244+1161G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591267 | ||||||
| chr7:2591328
|
C | G | 12 | a0008c0006t0023g0004a0008c0006t0023g0107a0008c0006t0023g0146others(9): Show | 12 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1244+1222C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591328 | ||||||
| chr7:2591332
|
G | C | 1 | a0004c0008t0070g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1244+1226G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591332 | ||||||
| chr7:2591338
|
T | C | 270 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(267): Show | 272 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1244+1232T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591338 | ||||||
| chr7:2591362
|
G | C | 11 | a0001c0010t0009g0005a0001c0010t0009g0121a0001c0010t0009g0122others(8): Show | 11 | HG00639.hp2 HG01192.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1244+1256G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591362 | ||||||
| chr7:2591371
|
G | A | 1 | a0006c0036t0033g0172 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1244+1265G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591371 | ||||||
| chr7:2591393
|
T | C | 13 | a0003c0025t0085g0110a0008c0006t0023g0004a0008c0006t0023g0107others(10): Show | 13 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1244+1287T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591393 | ||||||
| chr7:2591569
|
C | T | 12 | a0001c0029t0051g0171a0002c0049t0073g0054a0006c0009t0014g0267others(9): Show | 12 | HG01081.hp1 HG01109.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1245-1453C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591569 | ||||||
| chr7:2591611
|
G | A | 268 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(265): Show | 270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1245-1411G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591611 | ||||||
| chr7:2591616
|
A | AT | 41 | a0001c0001t0001g0284a0001c0001t0004g0180a0001c0001t0006g0236others(38): Show | 41 | HG00140.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1245-1384dupT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr7 | 2591616 | |||||
| chr7:2591616
|
AT | A | 6 | a0001c0001t0052g0060a0001c0001t0098g0371a0003c0005t0008g0189others(3): Show | 6 | HG01070.hp1 HG01884.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245-1384delT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr7 | 2591616 | |||||
| chr7:2591875
|
A | ACCTCCCA others(48): Show |
2 | a0002c0014t0002g0046a0002c0014t0003g0248 | 2 | NA18942.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1245-998_1245-944d others(57): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr7 | 2591875 | |||||
| chr7:2591875
|
ACCTCCCA others(48): Show |
A | 165 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(162): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1245-998_1245-944d others(57): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr7 | 2591875 | |||||
| chr7:2591875
|
ACCTCCCA others(103): Show |
A | 105 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(102): Show | 106 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1245-1053_1245-944 others(3): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr7 | 2591875 | |||||
| chr7:2591956
|
C | T | 2 | a0007c0012t0019g0139a0007c0012t0080g0135 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1245-1066C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2591956 | ||||||
| chr7:2591970
|
CCCGGGCC others(47): Show |
C | 1 | a0003c0005t0011g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1245-1049_1245-996 others(57): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr7 | 2591970 | |||||
| chr7:2592011
|
C | T | 3 | a0002c0015t0002g0075a0002c0015t0002g0076a0002c0015t0002g0097 | 3 | HG02055.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1245-1011C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592011 | ||||||
| chr7:2592028
|
G | A | 2 | a0001c0001t0005g0323a0001c0001t0028g0306 | 2 | HG00423.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1245-994G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592028 | ||||||
| chr7:2592095
|
G | A | 39 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(36): Show | 39 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1245-927G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592095 | ||||||
| chr7:2592277
|
G | A | 3 | a0002c0004t0002g0109a0002c0004t0003g0257a0002c0004t0003g0406 | 3 | HG01255.hp2 HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1245-745G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592277 | ||||||
| chr7:2592296
|
A | G | 265 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(262): Show | 267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1245-726A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592296 | ||||||
| chr7:2592388
|
T | C | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1245-634T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592388 | ||||||
| chr7:2592401
|
CAA | C | 84 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(81): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1245-620_1245-619d others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592401 | ||||||
| chr7:2592481
|
G | A | 9 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(6): Show | 9 | HG01496.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1245-541G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592481 | ||||||
| chr7:2592582
|
G | A | 3 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325 | 3 | HG01496.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1245-440G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592582 | ||||||
| chr7:2592631
|
A | C | 1 | a0006c0048t0065g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1245-391A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592631 | ||||||
| chr7:2592633
|
A | C | 1 | a0002c0049t0073g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1245-389A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592633 | ||||||
| chr7:2592644
|
C | T | 11 | a0001c0029t0051g0171a0002c0049t0073g0054a0006c0009t0014g0267others(8): Show | 11 | HG01081.hp1 HG01109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1245-378C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592644 | ||||||
| chr7:2592677
|
C | T | 1 | a0002c0004t0077g0104 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1245-345C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592677 | ||||||
| chr7:2592687
|
G | T | 1 | a0013c0024t0001g0203 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1245-335G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592687 | ||||||
| chr7:2592709
|
C | T | 1 | a0004c0008t0069g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1245-313C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592709 | ||||||
| chr7:2592752
|
C | G | 11 | a0002c0015t0002g0075a0002c0015t0002g0076a0002c0015t0002g0097others(8): Show | 11 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1245-270C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592752 | ||||||
| chr7:2592791
|
T | C | 1 | a0003c0005t0110g0258 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1245-231T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592791 | ||||||
| chr7:2592797
|
C | T | 1 | a0002c0002t0002g0010 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1245-225C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592797 | ||||||
| chr7:2592843
|
A | G | 266 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(263): Show | 268 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1245-179A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592843 | ||||||
| chr7:2592936
|
C | T | 1 | a0008c0006t0082g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1245-86C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592936 | ||||||
| chr7:2592998
|
C | T | 1 | a0002c0004t0108g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1245-24C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 14/21 | chr7 | 2592998 | ||||||
| chr7:2593138
|
G | A | 1 | a0003c0005t0008g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1349+12G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593138 | ||||||
| chr7:2593144
|
G | A | 5 | a0002c0002t0002g0029a0002c0002t0002g0049a0002c0002t0002g0069others(2): Show | 5 | HG01975.hp2 HG02004.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1349+18G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593144 | ||||||
| chr7:2593189
|
G | A | 1 | a0001c0003t0004g0098 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1349+63G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593189 | ||||||
| chr7:2593223
|
G | A | 7 | a0001c0019t0004g0093a0001c0019t0004g0105a0005c0007t0007g0262others(4): Show | 7 | HG00280.hp2 HG01074.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1349+97G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593223 | ||||||
| chr7:2593290
|
C | T | 1 | a0001c0003t0001g0313 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1349+164C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593290 | ||||||
| chr7:2593382
|
C | T | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1349+256C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593382 | ||||||
| chr7:2593495
|
G | A | 1 | a0001c0001t0016g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1349+369G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593495 | ||||||
| chr7:2593590
|
C | T | 2 | a0002c0004t0003g0223a0002c0004t0003g0238 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1349+464C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593590 | ||||||
| chr7:2593664
|
G | T | 1 | a0001c0003t0030g0155 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1349+538G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593664 | ||||||
| chr7:2593681
|
C | T | 3 | a0001c0047t0001g0308a0006c0009t0102g0214a0006c0048t0065g0165 | 3 | HG00639.hp2 HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1349+555C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593681 | ||||||
| chr7:2593694
|
G | A | 2 | a0006c0036t0033g0172a0006c0044t0033g0085 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1349+568G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593694 | ||||||
| chr7:2593787
|
G | T | 1 | a0002c0002t0003g0352 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1349+661G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593787 | ||||||
| chr7:2593822
|
C | T | 1 | a0002c0004t0003g0269 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1349+696C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593822 | ||||||
| chr7:2593838
|
T | C | 1 | a0001c0003t0036g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1349+712T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593838 | ||||||
| chr7:2593947
|
T | C | 5 | a0001c0047t0001g0308a0006c0009t0102g0214a0006c0036t0033g0172others(2): Show | 5 | HG00639.hp2 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1349+821T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593947 | ||||||
| chr7:2593962
|
C | T | 2 | a0002c0004t0002g0148a0005c0007t0007g0278 | 2 | HG02698.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1349+836C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593962 | ||||||
| chr7:2593977
|
T | C | 98 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(95): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1349+851T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593977 | ||||||
| chr7:2593994
|
G | C | 20 | a0001c0003t0027g0325a0001c0019t0004g0093a0001c0019t0004g0105others(17): Show | 20 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1349+868G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593994 | ||||||
| chr7:2593995
|
C | T | 34 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(31): Show | 34 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.1349+869C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2593995 | ||||||
| chr7:2594027
|
C | T | 1 | a0002c0002t0003g0402 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1350-859C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594027 | ||||||
| chr7:2594089
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1350-797G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594089 | ||||||
| chr7:2594203
|
T | C | 3 | a0004c0028t0067g0020a0018c0050t0066g0117a0019c0051t0081g0128 | 3 | HG02922.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1350-683T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594203 | ||||||
| chr7:2594217
|
G | C | 1 | a0005c0007t0007g0067 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1350-669G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594217 | ||||||
| chr7:2594224
|
T | C | 1 | a0007c0016t0035g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1350-662T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594224 | ||||||
| chr7:2594237
|
G | A | 2 | a0002c0004t0003g0223a0002c0004t0003g0238 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1350-649G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594237 | ||||||
| chr7:2594271
|
A | C | 1 | a0003c0005t0008g0191 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1350-615A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594271 | ||||||
| chr7:2594342
|
C | G | 2 | a0002c0015t0002g0075a0018c0050t0066g0117 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1350-544C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594342 | ||||||
| chr7:2594368
|
AT | A | 135 | a0001c0001t0001g0210a0001c0001t0004g0036a0001c0001t0004g0047others(132): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1350-509delT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr7 | 2594368 | |||||
| chr7:2594417
|
A | G | 2 | a0001c0003t0026g0234a0004c0008t0064g0197 | 2 | HG03209.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1350-469A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594417 | ||||||
| chr7:2594450
|
A | G | 2 | a0002c0049t0073g0054a0006c0009t0102g0214 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1350-436A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594450 | ||||||
| chr7:2594497
|
C | T | 1 | a0002c0002t0003g0340 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1350-389C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594497 | ||||||
| chr7:2594569
|
T | G | 1 | a0001c0001t0016g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1350-317T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594569 | ||||||
| chr7:2594630
|
G | T | 2 | a0001c0001t0058g0307a0001c0001t0099g0305 | 2 | HG00438.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1350-256G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594630 | ||||||
| chr7:2594631
|
G | C | 1 | a0006c0048t0065g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1350-255G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594631 | ||||||
| chr7:2594648
|
C | T | 1 | a0002c0002t0078g0062 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1350-238C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594648 | ||||||
| chr7:2594692
|
C | T | 1 | a0010c0017t0007g0092 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1350-194C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594692 | ||||||
| chr7:2594697
|
G | A | 3 | a0002c0004t0002g0163a0002c0004t0003g0364a0002c0004t0039g0356 | 3 | HG00639.hp1 HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1350-189G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594697 | ||||||
| chr7:2594750
|
A | G | 8 | a0001c0029t0051g0171a0002c0049t0073g0054a0006c0009t0014g0267others(5): Show | 8 | HG01081.hp1 HG01109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1350-136A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594750 | ||||||
| chr7:2594796
|
C | T | 8 | a0002c0004t0002g0148a0002c0004t0012g0294a0002c0004t0012g0300others(5): Show | 8 | HG00408.hp2 HG02074.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.1350-90C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594796 | ||||||
| chr7:2594797
|
G | A | 4 | a0004c0008t0010g0022a0004c0008t0010g0052a0004c0008t0064g0197others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350-89G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594797 | ||||||
| chr7:2594799
|
C | G | 5 | a0004c0008t0010g0022a0004c0008t0010g0052a0004c0008t0064g0197others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1350-87C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594799 | ||||||
| chr7:2594806
|
G | A | 1 | a0004c0008t0010g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1350-80G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594806 | ||||||
| chr7:2594830
|
G | A | 1 | a0002c0002t0018g0132 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1350-56G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 15/21 | chr7 | 2594830 | ||||||
| chr7:2595034
|
G | A | 8 | a0003c0005t0011g0194a0003c0005t0011g0195a0003c0005t0011g0196others(5): Show | 8 | HG00621.hp1 HG03471.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.1440+58G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595034 | ||||||
| chr7:2595144
|
C | T | 1 | a0008c0006t0024g0112 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1440+168C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595144 | ||||||
| chr7:2595149
|
T | G | 13 | a0005c0007t0007g0002a0005c0007t0007g0067a0005c0007t0007g0101others(10): Show | 13 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1440+173T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595149 | ||||||
| chr7:2595183
|
C | T | 1 | a0001c0001t0005g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1440+207C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595183 | ||||||
| chr7:2595219
|
G | A | 3 | a0006c0009t0102g0214a0007c0039t0092g0013a0018c0050t0066g0117 | 3 | HG02258.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1440+243G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595219 | ||||||
| chr7:2595263
|
C | T | 1 | a0001c0001t0005g0102 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1440+287C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595263 | ||||||
| chr7:2595319
|
A | G | 12 | a0003c0005t0011g0050a0003c0005t0011g0181a0003c0005t0011g0186others(9): Show | 12 | HG00621.hp1 NA18939.hp2 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.1440+343A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595319 | ||||||
| chr7:2595421
|
G | C | 4 | a0006c0009t0102g0214a0006c0048t0065g0165a0007c0039t0092g0013others(1): Show | 4 | HG00639.hp2 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+445G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595421 | ||||||
| chr7:2595433
|
C | T | 32 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(29): Show | 32 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1440+457C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595433 | ||||||
| chr7:2595442
|
G | A | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+466G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595442 | ||||||
| chr7:2595451
|
C | G | 43 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(40): Show | 44 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1440+475C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595451 | ||||||
| chr7:2595481
|
TAGCAGGG others(12): Show |
T | 2 | a0004c0008t0010g0022a0004c0008t0010g0052 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1440+517_1440+535d others(21): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 2595481 | |||||
| chr7:2595578
|
C | T | 7 | a0003c0005t0011g0194a0003c0005t0011g0195a0003c0005t0011g0196others(4): Show | 7 | HG00621.hp1 NA18939.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1440+602C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595578 | ||||||
| chr7:2595587
|
G | A | 7 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(4): Show | 7 | HG01496.hp2 HG02451.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1440+611G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595587 | ||||||
| chr7:2595600
|
C | T | 129 | a0001c0001t0052g0060a0001c0029t0051g0171a0002c0002t0002g0006others(126): Show | 130 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1440+624C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595600 | ||||||
| chr7:2595679
|
CCCTGGAG others(105): Show |
C | 1 | a0001c0011t0001g0413 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1440+743_1440+854d others(2): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 2595679 | |||||
| chr7:2595804
|
C | T | 41 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(38): Show | 41 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.1440+828C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595804 | ||||||
| chr7:2595815
|
T | C | 5 | a0007c0012t0019g0120a0007c0012t0019g0138a0007c0012t0019g0139others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+839T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595815 | ||||||
| chr7:2595857
|
A | ACAGCCAT others(47): Show |
33 | a0001c0003t0001g0287a0001c0003t0001g0336a0001c0003t0004g0099others(30): Show | 34 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1440+909_1440+962d others(56): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 2595857 | |||||
| chr7:2595857
|
A | ACAGCCAT others(101): Show |
1 | a0003c0005t0008g0189 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1440+962_1440+963i others(110): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 2595857 | |||||
| chr7:2595859
|
A | G | 7 | a0003c0020t0083g0159a0003c0020t0084g0160a0008c0006t0023g0004others(4): Show | 7 | HG01167.hp2 HG01243.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1440+883A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595859 | ||||||
| chr7:2595937
|
G | A | 6 | a0004c0028t0067g0020a0007c0012t0019g0120a0007c0012t0019g0138others(3): Show | 6 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1440+961G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595937 | ||||||
| chr7:2595974
|
C | T | 1 | a0020c0040t0001g0310 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1440+998C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2595974 | ||||||
| chr7:2596162
|
G | A | 3 | a0006c0009t0102g0214a0006c0048t0065g0165a0007c0039t0092g0013 | 3 | HG00639.hp2 HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1440+1186G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2596162 | ||||||
| chr7:2596177
|
C | G | 102 | a0001c0001t0001g0284a0001c0001t0005g0028a0001c0001t0005g0041others(99): Show | 102 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1440+1201C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2596177 | ||||||
| chr7:2596178
|
G | A | 2 | a0002c0004t0077g0104a0002c0004t0108g0259 | 2 | HG00738.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1440+1202G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2596178 | ||||||
| chr7:2596277
|
AAGAG | A | 3 | a0001c0010t0009g0121a0001c0010t0009g0122a0018c0050t0066g0117 | 3 | HG02486.hp1 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1440+1305_1440+130 others(8): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 2596277 | |||||
| chr7:2596314
|
G | GGA | 6 | a0001c0003t0093g0249a0005c0007t0007g0101a0005c0007t0007g0106others(3): Show | 6 | HG02258.hp1 HG02293.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.1440+1359_1440+136 others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 2596314 | |||||
| chr7:2596314
|
GGAGA | G | 6 | a0002c0002t0002g0156a0002c0002t0015g0316a0002c0002t0015g0321others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1440+1357_1440+136 others(8): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 2596314 | |||||
| chr7:2596399
|
AT | A | 23 | a0001c0001t0004g0039a0001c0001t0098g0371a0001c0003t0027g0271others(20): Show | 24 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1440+1442delT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 2596399 | |||||
| chr7:2596399
|
ATT | A | 13 | a0005c0007t0007g0002a0005c0007t0007g0101a0005c0007t0007g0106others(10): Show | 13 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1440+1441_1440+144 others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 2596399 | |||||
| chr7:2596399
|
ATTT | A | 149 | a0001c0001t0052g0060a0001c0029t0051g0171a0002c0002t0002g0006others(146): Show | 150 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.1440+1440_1440+144 others(7): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 2596399 | |||||
| chr7:2596633
|
C | A | 3 | a0002c0002t0002g0133a0002c0002t0002g0153a0002c0002t0002g0158 | 3 | NA18968.hp2 NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1440+1657C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2596633 | ||||||
| chr7:2596647
|
G | A | 136 | a0001c0001t0052g0060a0001c0029t0051g0171a0002c0002t0002g0006others(133): Show | 137 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1440+1671G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2596647 | ||||||
| chr7:2596711
|
G | A | 13 | a0002c0002t0002g0126a0002c0002t0002g0134a0002c0002t0003g0253others(10): Show | 13 | HG02083.hp2 NA18950.hp1 NA18960.hp2 others(10): Show |
intron_variant | MODIFIER | c.1440+1735G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2596711 | ||||||
| chr7:2596739
|
A | G | 1 | a0021c0027t0047g0243 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1441-1726A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2596739 | ||||||
| chr7:2596751
|
C | T | 129 | a0001c0029t0051g0171a0002c0002t0002g0006a0002c0002t0002g0010others(126): Show | 130 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1441-1714C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2596751 | ||||||
| chr7:2596886
|
A | G | 1 | a0026c0032t0021g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1441-1579A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2596886 | ||||||
| chr7:2596888
|
T | G | 43 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(40): Show | 44 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1441-1577T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2596888 | ||||||
| chr7:2596997
|
A | T | 1 | a0002c0002t0002g0029 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1441-1468A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2596997 | ||||||
| chr7:2597043
|
G | C | 1 | a0001c0022t0090g0082 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1441-1422G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597043 | ||||||
| chr7:2597055
|
C | T | 60 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(57): Show | 60 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.1441-1410C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597055 | ||||||
| chr7:2597059
|
G | A | 1 | a0006c0048t0065g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1441-1406G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597059 | ||||||
| chr7:2597084
|
G | T | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441-1381G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597084 | ||||||
| chr7:2597101
|
C | T | 3 | a0006c0048t0065g0165a0007c0039t0092g0013a0018c0050t0066g0117 | 3 | HG00639.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1441-1364C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597101 | ||||||
| chr7:2597104
|
G | A | 1 | a0005c0007t0007g0067 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1441-1361G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597104 | ||||||
| chr7:2597122
|
G | T | 2 | a0008c0006t0023g0146a0008c0006t0082g0108 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1441-1343G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597122 | ||||||
| chr7:2597261
|
C | G | 109 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(106): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1441-1204C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597261 | ||||||
| chr7:2597275
|
G | A | 1 | a0001c0003t0030g0155 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1441-1190G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597275 | ||||||
| chr7:2597430
|
A | G | 189 | a0001c0003t0001g0324a0001c0003t0001g0389a0001c0010t0009g0005others(186): Show | 191 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.1441-1035A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597430 | ||||||
| chr7:2597505
|
G | A | 43 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(40): Show | 44 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1441-960G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597505 | ||||||
| chr7:2597538
|
C | T | 2 | a0004c0008t0064g0197a0004c0008t0070g0198 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1441-927C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597538 | ||||||
| chr7:2597626
|
A | G | 2 | a0003c0005t0042g0369a0003c0005t0042g0378 | 2 | HG01981.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1441-839A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597626 | ||||||
| chr7:2597628
|
G | GGAT | 5 | a0007c0012t0019g0120a0007c0012t0019g0138a0007c0012t0019g0139others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-833_1441-831d others(5): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 2597628 | |||||
| chr7:2597717
|
G | A | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441-748G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597717 | ||||||
| chr7:2597725
|
C | T | 1 | a0001c0003t0030g0155 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1441-740C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597725 | ||||||
| chr7:2597726
|
G | A | 2 | a0007c0016t0035g0143a0007c0016t0050g0266 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1441-739G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597726 | ||||||
| chr7:2597868
|
A | T | 1 | a0001c0001t0001g0210 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1441-597A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597868 | ||||||
| chr7:2597928
|
A | C | 1 | a0027c0052t0001g0344 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1441-537A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597928 | ||||||
| chr7:2597944
|
A | G | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441-521A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597944 | ||||||
| chr7:2597949
|
T | C | 8 | a0006c0009t0014g0267a0006c0009t0014g0280a0006c0009t0014g0303others(5): Show | 8 | HG01081.hp1 HG02145.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1441-516T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2597949 | ||||||
| chr7:2598372
|
C | T | 2 | a0001c0029t0051g0171a0002c0049t0073g0054 | 2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1441-93C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 16/21 | chr7 | 2598372 | ||||||
| chr7:2598644
|
C | T | 4 | a0006c0009t0102g0214a0006c0048t0065g0165a0007c0039t0092g0013others(1): Show | 4 | HG00639.hp2 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+12C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2598644 | ||||||
| chr7:2598665
|
C | G | 5 | a0006c0009t0014g0267a0006c0009t0014g0303a0006c0009t0117g0091others(2): Show | 5 | HG01081.hp1 HG02145.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1608+33C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2598665 | ||||||
| chr7:2598713
|
C | G | 106 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(103): Show | 106 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1608+81C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2598713 | ||||||
| chr7:2598743
|
T | G | 5 | a0002c0004t0077g0104a0002c0004t0107g0289a0002c0004t0108g0259others(2): Show | 5 | HG00738.hp1 HG02735.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1608+111T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2598743 | ||||||
| chr7:2598905
|
G | A | 1 | a0001c0001t0006g0255 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1608+273G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2598905 | ||||||
| chr7:2598957
|
G | C | 1 | a0002c0002t0003g0340 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1608+325G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2598957 | ||||||
| chr7:2598999
|
C | A | 1 | a0001c0003t0004g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1608+367C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2598999 | ||||||
| chr7:2599004
|
C | G | 2 | a0001c0001t0031g0142a0001c0001t0055g0170 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1608+372C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599004 | ||||||
| chr7:2599046
|
C | T | 1 | a0002c0002t0002g0133 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1608+414C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599046 | ||||||
| chr7:2599064
|
A | G | 38 | a0001c0003t0001g0324a0001c0003t0001g0389a0002c0002t0002g0133others(35): Show | 39 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.1608+432A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599064 | ||||||
| chr7:2599527
|
C | T | 2 | a0001c0001t0060g0042a0001c0001t0100g0199 | 2 | HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1608+895C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599527 | ||||||
| chr7:2599545
|
G | T | 1 | a0003c0005t0041g0330 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1608+913G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599545 | ||||||
| chr7:2599572
|
C | T | 1 | a0001c0001t0001g0411 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1608+940C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599572 | ||||||
| chr7:2599607
|
C | T | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+975C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599607 | ||||||
| chr7:2599618
|
T | C | 231 | a0001c0003t0001g0324a0001c0003t0001g0389a0001c0003t0027g0271others(228): Show | 233 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.1608+986T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599618 | ||||||
| chr7:2599652
|
A | G | 2 | a0001c0003t0001g0265a0001c0003t0001g0279 | 2 | HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1608+1020A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599652 | ||||||
| chr7:2599685
|
C | T | 1 | a0008c0006t0082g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1608+1053C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599685 | ||||||
| chr7:2599687
|
G | A | 1 | a0002c0002t0049g0399 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1608+1055G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599687 | ||||||
| chr7:2599813
|
G | A | 1 | a0001c0001t0032g0079 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1608+1181G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599813 | ||||||
| chr7:2599845
|
G | A | 1 | a0002c0049t0073g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1608+1213G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599845 | ||||||
| chr7:2599953
|
A | C | 364 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(361): Show | 366 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.1608+1321A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2599953 | ||||||
| chr7:2600156
|
G | A | 41 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(38): Show | 42 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1609-1285G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600156 | ||||||
| chr7:2600290
|
G | A | 1 | a0002c0015t0002g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1609-1151G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600290 | ||||||
| chr7:2600318
|
G | A | 5 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0166others(2): Show | 5 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1609-1123G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600318 | ||||||
| chr7:2600329
|
A | G | 1 | a0004c0028t0067g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1609-1112A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600329 | ||||||
| chr7:2600360
|
C | T | 41 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(38): Show | 42 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1609-1081C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600360 | ||||||
| chr7:2600390
|
A | G | 8 | a0001c0010t0009g0005a0001c0010t0009g0121a0001c0010t0009g0122others(5): Show | 8 | HG01192.hp2 HG01243.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1609-1051A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600390 | ||||||
| chr7:2600507
|
C | T | 149 | a0001c0003t0001g0324a0001c0003t0001g0389a0001c0029t0051g0171others(146): Show | 150 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.1609-934C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600507 | ||||||
| chr7:2600536
|
G | A | 1 | a0003c0005t0113g0283 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1609-905G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600536 | ||||||
| chr7:2600562
|
C | G | 38 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(35): Show | 38 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1609-879C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600562 | ||||||
| chr7:2600744
|
A | C | 204 | a0001c0003t0001g0324a0001c0003t0001g0389a0001c0010t0009g0005others(201): Show | 206 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.1609-697A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600744 | ||||||
| chr7:2600825
|
C | T | 1 | a0002c0002t0015g0316 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1609-616C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600825 | ||||||
| chr7:2600899
|
C | T | 232 | a0001c0003t0001g0324a0001c0003t0001g0389a0001c0003t0027g0271others(229): Show | 234 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.1609-542C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600899 | ||||||
| chr7:2600961
|
G | T | 41 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(38): Show | 42 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1609-480G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600961 | ||||||
| chr7:2600988
|
C | G | 1 | a0002c0002t0078g0062 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1609-453C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2600988 | ||||||
| chr7:2601033
|
G | C | 1 | a0002c0002t0029g0031 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1609-408G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2601033 | ||||||
| chr7:2601187
|
G | A | 218 | a0001c0003t0001g0324a0001c0003t0001g0389a0001c0003t0027g0271others(215): Show | 220 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1609-254G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2601187 | ||||||
| chr7:2601263
|
T | C | 196 | a0001c0003t0001g0324a0001c0003t0001g0389a0001c0003t0027g0271others(193): Show | 197 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.1609-178T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2601263 | ||||||
| chr7:2601307
|
C | T | 1 | a0006c0009t0102g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1609-134C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2601307 | ||||||
| chr7:2601310
|
G | A | 6 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(3): Show | 6 | HG01496.hp2 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1609-131G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2601310 | ||||||
| chr7:2601312
|
G | C | 1 | a0005c0007t0089g0077 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1609-129G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2601312 | ||||||
| chr7:2601351
|
G | C | 294 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(291): Show | 296 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.1609-90G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | chr7 | 2601351 | ||||||
| chr7:2601425
|
C | CT | 36 | a0001c0001t0004g0027a0001c0003t0027g0271a0001c0003t0027g0272others(33): Show | 36 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(33): Show |
splice_region_variant&intron_variant | LOW | c.1609-5dupT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 2601425 | |||||
| chr7:2601496
|
C | T | 2 | a0004c0008t0064g0197a0004c0008t0070g0198 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1632+32C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2601496 | ||||||
| chr7:2601500
|
T | C | 1 | a0002c0002t0003g0355 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1632+36T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2601500 | ||||||
| chr7:2601597
|
T | C | 1 | a0005c0007t0115g0277 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1632+133T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2601597 | ||||||
| chr7:2601726
|
T | C | 1 | a0007c0039t0092g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1632+262T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2601726 | ||||||
| chr7:2601738
|
C | T | 41 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(38): Show | 42 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1632+274C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2601738 | ||||||
| chr7:2601760
|
G | C | 194 | a0001c0003t0001g0324a0001c0003t0001g0389a0001c0003t0027g0271others(191): Show | 195 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.1632+296G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2601760 | ||||||
| chr7:2601841
|
C | T | 191 | a0001c0003t0001g0324a0001c0003t0001g0389a0001c0003t0027g0271others(188): Show | 192 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.1632+377C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2601841 | ||||||
| chr7:2601856
|
T | C | 5 | a0007c0012t0019g0120a0007c0012t0019g0138a0007c0012t0019g0139others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1632+392T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2601856 | ||||||
| chr7:2601868
|
AC | A | 5 | a0007c0012t0019g0120a0007c0012t0019g0138a0007c0012t0019g0139others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1632+406delC | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr7 | 2601868 | |||||
| chr7:2601951
|
A | C | 2 | a0009c0013t0022g0084a0009c0013t0068g0100 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1632+487A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2601951 | ||||||
| chr7:2601965
|
A | C | 1 | a0005c0007t0007g0275 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1632+501A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2601965 | ||||||
| chr7:2601991
|
T | G | 13 | a0005c0007t0007g0002a0005c0007t0007g0067a0005c0007t0007g0101others(10): Show | 13 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1632+527T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2601991 | ||||||
| chr7:2602023
|
G | A | 9 | a0001c0029t0051g0171a0004c0008t0010g0015a0004c0008t0010g0016others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1632+559G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602023 | ||||||
| chr7:2602050
|
G | A | 2 | a0001c0001t0006g0226a0001c0001t0006g0236 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1632+586G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602050 | ||||||
| chr7:2602090
|
CG | C | 7 | a0005c0007t0007g0002a0005c0007t0007g0067a0005c0007t0007g0101others(4): Show | 7 | HG00733.hp2 HG01070.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1632+630delG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr7 | 2602090 | |||||
| chr7:2602121
|
C | T | 1 | a0002c0049t0073g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1632+657C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602121 | ||||||
| chr7:2602149
|
G | T | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1632+685G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602149 | ||||||
| chr7:2602170
|
G | A | 1 | a0001c0019t0004g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1632+706G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602170 | ||||||
| chr7:2602316
|
G | A | 1 | a0004c0008t0070g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1632+852G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602316 | ||||||
| chr7:2602335
|
G | A | 1 | a0003c0005t0041g0337 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1632+871G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602335 | ||||||
| chr7:2602416
|
C | T | 58 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(55): Show | 58 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.1632+952C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602416 | ||||||
| chr7:2602481
|
T | C | 364 | a0001c0001t0001g0343a0001c0001t0005g0028a0001c0001t0005g0041others(361): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1632+1017T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602481 | ||||||
| chr7:2602508
|
A | G | 242 | a0001c0001t0001g0207a0001c0001t0001g0224a0001c0001t0001g0347others(239): Show | 244 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.1632+1044A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602508 | ||||||
| chr7:2602521
|
C | T | 5 | a0008c0006t0023g0004a0008c0006t0023g0107a0008c0006t0023g0146others(2): Show | 5 | HG01167.hp2 HG01243.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1632+1057C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602521 | ||||||
| chr7:2602541
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1632+1077A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602541 | ||||||
| chr7:2602553
|
A | C | 302 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(299): Show | 304 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1632+1089A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602553 | ||||||
| chr7:2602555
|
G | A | 142 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0029others(139): Show | 143 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1632+1091G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602555 | ||||||
| chr7:2602589
|
C | G | 1 | a0001c0003t0004g0098 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1632+1125C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602589 | ||||||
| chr7:2602732
|
C | T | 6 | a0003c0025t0085g0110a0008c0006t0024g0112a0008c0006t0024g0127others(3): Show | 6 | HG01192.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1632+1268C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602732 | ||||||
| chr7:2602837
|
A | G | 236 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(233): Show | 238 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.1632+1373A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602837 | ||||||
| chr7:2602854
|
C | T | 1 | a0001c0003t0001g0336 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1632+1390C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602854 | ||||||
| chr7:2602914
|
C | T | 34 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(31): Show | 34 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1632+1450C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602914 | ||||||
| chr7:2602915
|
G | A | 1 | a0002c0002t0003g0401 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1632+1451G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2602915 | ||||||
| chr7:2603079
|
A | T | 1 | a0006c0009t0102g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1632+1615A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603079 | ||||||
| chr7:2603082
|
C | T | 4 | a0007c0016t0035g0143a0007c0016t0050g0266a0007c0016t0079g0145others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1632+1618C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603082 | ||||||
| chr7:2603116
|
A | G | 2 | a0002c0004t0003g0223a0002c0004t0003g0238 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1632+1652A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603116 | ||||||
| chr7:2603217
|
T | TGCCCAGG others(19): Show |
1 | a0002c0002t0003g0353 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1633-1661_1633-163 others(30): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr7 | 2603217 | |||||
| chr7:2603244
|
G | A | 42 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(39): Show | 43 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1633-1637G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603244 | ||||||
| chr7:2603433
|
G | A | 2 | a0001c0003t0001g0260a0001c0003t0001g0313 | 2 | HG01433.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1633-1448G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603433 | ||||||
| chr7:2603450
|
T | C | 151 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0029others(148): Show | 152 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.1633-1431T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603450 | ||||||
| chr7:2603466
|
A | G | 236 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(233): Show | 238 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.1633-1415A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603466 | ||||||
| chr7:2603473
|
TTC | T | 58 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(55): Show | 58 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.1633-1403_1633-140 others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr7 | 2603473 | |||||
| chr7:2603493
|
A | G | 236 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(233): Show | 238 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.1633-1388A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603493 | ||||||
| chr7:2603512
|
T | C | 2 | a0001c0001t0031g0142a0001c0001t0055g0170 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1633-1369T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603512 | ||||||
| chr7:2603544
|
T | C | 1 | a0001c0003t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1633-1337T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603544 | ||||||
| chr7:2603597
|
C | T | 1 | a0006c0009t0102g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1633-1284C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603597 | ||||||
| chr7:2603664
|
C | T | 1 | a0002c0002t0002g0033 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1633-1217C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603664 | ||||||
| chr7:2603707
|
G | A | 42 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(39): Show | 43 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1633-1174G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603707 | ||||||
| chr7:2603718
|
C | T | 46 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(43): Show | 47 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1633-1163C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603718 | ||||||
| chr7:2603811
|
G | A | 2 | a0007c0039t0092g0013a0018c0050t0066g0117 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1633-1070G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603811 | ||||||
| chr7:2603919
|
A | G | 2 | a0001c0001t0006g0226a0001c0001t0006g0236 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1633-962A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603919 | ||||||
| chr7:2603932
|
T | C | 1 | a0023c0043t0018g0147 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1633-949T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603932 | ||||||
| chr7:2603933
|
C | A | 1 | a0023c0043t0018g0147 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1633-948C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603933 | ||||||
| chr7:2603962
|
T | C | 243 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(240): Show | 245 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.1633-919T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603962 | ||||||
| chr7:2603973
|
T | C | 293 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(290): Show | 295 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1633-908T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2603973 | ||||||
| chr7:2603989
|
C | CT | 38 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(35): Show | 39 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1633-875dupT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr7 | 2603989 | |||||
| chr7:2603989
|
CT | C | 307 | a0001c0001t0001g0212a0001c0001t0001g0343a0001c0001t0005g0028others(304): Show | 308 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.1633-875delT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr7 | 2603989 | |||||
| chr7:2604025
|
G | A | 1 | a0004c0028t0067g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1633-856G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2604025 | ||||||
| chr7:2604132
|
G | T | 1 | a0006c0048t0065g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1633-749G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2604132 | ||||||
| chr7:2604138
|
G | GC | 413 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(410): Show | 415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.1633-742dupC | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr7 | 2604138 | |||||
| chr7:2604299
|
C | T | 1 | a0001c0003t0001g0229 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1633-582C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2604299 | ||||||
| chr7:2604546
|
C | T | 6 | a0001c0001t0017g0140a0001c0001t0017g0144a0001c0001t0021g0129others(3): Show | 6 | HG02280.hp2 HG02717.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1633-335C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2604546 | ||||||
| chr7:2604693
|
A | G | 294 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(291): Show | 296 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.1633-188A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2604693 | ||||||
| chr7:2604756
|
C | T | 2 | a0001c0001t0004g0180a0001c0047t0001g0308 | 2 | HG00741.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1633-125C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2604756 | ||||||
| chr7:2604799
|
C | G | 1 | a0012c0023t0001g0288 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1633-82C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2604799 | ||||||
| chr7:2604870
|
T | C | 1 | a0019c0051t0081g0128 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1633-11T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 18/21 | chr7 | 2604870 | ||||||
| chr7:2605012
|
G | A | 1 | a0007c0039t0092g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1743+21G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605012 | ||||||
| chr7:2605016
|
C | A | 2 | a0001c0001t0032g0079a0001c0030t0032g0068 | 2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.1743+25C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605016 | ||||||
| chr7:2605045
|
G | A | 53 | a0001c0001t0017g0083a0001c0001t0017g0140a0001c0001t0017g0144others(50): Show | 54 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1743+54G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605045 | ||||||
| chr7:2605067
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1743+76G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605067 | ||||||
| chr7:2605069
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1743+78A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605069 | ||||||
| chr7:2605202
|
G | A | 1 | a0002c0002t0013g0400 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1743+211G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605202 | ||||||
| chr7:2605212
|
G | C | 288 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(285): Show | 290 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1743+221G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605212 | ||||||
| chr7:2605286
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1743+295C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605286 | ||||||
| chr7:2605297
|
C | G | 1 | a0001c0001t0006g0285 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1743+306C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605297 | ||||||
| chr7:2605332
|
T | A | 1 | a0001c0001t0004g0037 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1743+341T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605332 | ||||||
| chr7:2605334
|
T | G | 11 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(8): Show | 11 | HG01496.hp2 HG02451.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1743+343T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605334 | ||||||
| chr7:2605394
|
G | A | 2 | a0001c0001t0004g0180a0001c0047t0001g0308 | 2 | HG00741.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1743+403G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605394 | ||||||
| chr7:2605493
|
G | A | 10 | a0001c0029t0051g0171a0002c0004t0003g0221a0004c0008t0010g0015others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1744-383G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605493 | ||||||
| chr7:2605498
|
C | T | 199 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0029others(196): Show | 201 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.1744-378C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605498 | ||||||
| chr7:2605567
|
T | C | 292 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(289): Show | 294 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1744-309T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605567 | ||||||
| chr7:2605606
|
C | T | 1 | a0001c0001t0059g0393 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1744-270C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605606 | ||||||
| chr7:2605636
|
G | A | 1 | a0002c0004t0012g0294 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1744-240G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605636 | ||||||
| chr7:2605636
|
G | GTAAA | 188 | a0001c0001t0006g0281a0001c0001t0038g0328a0002c0002t0002g0006others(185): Show | 190 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.1744-213_1744-210d others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr7 | 2605636 | |||||
| chr7:2605636
|
G | GTAAATAA others(1): Show |
3 | a0002c0002t0003g0402a0003c0005t0011g0188a0024c0042t0074g0059 | 3 | NA18971.hp2 NA18988.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1744-217_1744-210d others(10): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr7 | 2605636 | |||||
| chr7:2605636
|
GTAAA | G | 5 | a0006c0036t0033g0172a0006c0044t0033g0085a0009c0013t0022g0051others(2): Show | 5 | HG02145.hp1 HG03453.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1744-213_1744-210d others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr7 | 2605636 | |||||
| chr7:2605636
|
GTAAATAA others(1): Show |
G | 12 | a0001c0029t0051g0171a0004c0008t0010g0015a0004c0008t0010g0016others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1744-217_1744-210d others(10): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr7 | 2605636 | |||||
| chr7:2605689
|
T | A | 1 | a0002c0002t0003g0301 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1744-187T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605689 | ||||||
| chr7:2605740
|
C | T | 16 | a0002c0015t0002g0075a0002c0015t0002g0076a0002c0015t0002g0097others(13): Show | 16 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1744-136C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605740 | ||||||
| chr7:2605791
|
C | T | 86 | a0002c0002t0002g0006a0002c0002t0002g0029a0002c0002t0002g0033others(83): Show | 86 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1744-85C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605791 | ||||||
| chr7:2605815
|
G | A | 1 | a0001c0001t0016g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1744-61G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605815 | ||||||
| chr7:2605828
|
G | A | 1 | a0002c0015t0002g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1744-48G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 19/21 | chr7 | 2605828 | ||||||
| chr7:2606123
|
G | A | 1 | a0013c0024t0001g0201 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1865+126G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606123 | ||||||
| chr7:2606182
|
A | T | 1 | a0023c0043t0018g0147 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1865+185A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606182 | ||||||
| chr7:2606215
|
C | T | 1 | a0004c0008t0010g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1865+218C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606215 | ||||||
| chr7:2606251
|
G | T | 3 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0068g0100 | 3 | HG03453.hp2 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1865+254G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606251 | ||||||
| chr7:2606313
|
C | T | 13 | a0005c0007t0007g0002a0005c0007t0007g0067a0005c0007t0007g0101others(10): Show | 13 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1865+316C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606313 | ||||||
| chr7:2606338
|
C | T | 41 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(38): Show | 42 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1865+341C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606338 | ||||||
| chr7:2606360
|
G | C | 1 | a0001c0001t0001g0343 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1865+363G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606360 | ||||||
| chr7:2606371
|
C | T | 43 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(40): Show | 44 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1865+374C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606371 | ||||||
| chr7:2606393
|
A | C | 1 | a0008c0006t0023g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1865+396A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606393 | ||||||
| chr7:2606545
|
C | G | 51 | a0001c0001t0001g0343a0001c0001t0094g0409a0001c0003t0001g0202others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1865+548C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606545 | ||||||
| chr7:2606589
|
A | G | 157 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0029others(154): Show | 158 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.1866-535A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606589 | ||||||
| chr7:2606612
|
T | C | 202 | a0001c0029t0051g0171a0002c0002t0002g0006a0002c0002t0002g0010others(199): Show | 204 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.1866-512T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606612 | ||||||
| chr7:2606717
|
T | C | 266 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(263): Show | 268 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1866-407T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606717 | ||||||
| chr7:2606728
|
G | C | 13 | a0005c0007t0007g0002a0005c0007t0007g0067a0005c0007t0007g0101others(10): Show | 13 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1866-396G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606728 | ||||||
| chr7:2606746
|
T | C | 1 | a0001c0003t0001g0239 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1866-378T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606746 | ||||||
| chr7:2606751
|
G | A | 1 | a0001c0001t0017g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1866-373G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606751 | ||||||
| chr7:2606789
|
G | A | 9 | a0001c0029t0051g0171a0004c0008t0010g0015a0004c0008t0010g0016others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1866-335G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606789 | ||||||
| chr7:2606914
|
G | A | 1 | a0018c0050t0066g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1866-210G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606914 | ||||||
| chr7:2606938
|
C | T | 3 | a0002c0015t0002g0075a0002c0015t0002g0076a0002c0015t0002g0097 | 3 | HG02055.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1866-186C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2606938 | ||||||
| chr7:2607089
|
A | G | 201 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0029others(198): Show | 203 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.1866-35A>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 20/21 | chr7 | 2607089 | ||||||
| chr7:2607311
|
C | T | 1 | a0002c0002t0002g0006 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1969+84C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607311 | ||||||
| chr7:2607316
|
T | G | 202 | a0001c0029t0051g0171a0002c0002t0002g0006a0002c0002t0002g0010others(199): Show | 204 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.1969+89T>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607316 | ||||||
| chr7:2607332
|
G | A | 1 | a0019c0051t0081g0128 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1969+105G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607332 | ||||||
| chr7:2607373
|
G | A | 43 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(40): Show | 44 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1969+146G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607373 | ||||||
| chr7:2607414
|
C | G | 58 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(55): Show | 58 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.1969+187C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607414 | ||||||
| chr7:2607416
|
A | T | 1 | a0023c0043t0018g0147 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1969+189A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607416 | ||||||
| chr7:2607424
|
C | A | 1 | a0006c0048t0065g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1969+197C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607424 | ||||||
| chr7:2607442
|
C | T | 1 | a0002c0002t0002g0010 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1969+215C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607442 | ||||||
| chr7:2607527
|
T | A | 1 | a0024c0042t0074g0059 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1969+300T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607527 | ||||||
| chr7:2607551
|
T | C | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1969+324T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607551 | ||||||
| chr7:2607679
|
A | AG | 413 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(410): Show | 415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.1969+454dupG | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr7 | 2607679 | |||||
| chr7:2607691
|
TC | T | 155 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0029others(152): Show | 156 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.1969+465delC | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607691 | ||||||
| chr7:2607743
|
G | C | 165 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0029others(162): Show | 166 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.1969+516G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607743 | ||||||
| chr7:2607769
|
A | C | 6 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0211others(3): Show | 6 | HG01943.hp1 HG01952.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1969+542A>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607769 | ||||||
| chr7:2607771
|
G | A | 2 | a0006c0009t0102g0214a0006c0048t0065g0165 | 2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1969+544G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607771 | ||||||
| chr7:2607818
|
A | T | 1 | a0020c0040t0001g0310 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1969+591A>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607818 | ||||||
| chr7:2607862
|
G | C | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1969+635G>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607862 | ||||||
| chr7:2607866
|
G | A | 131 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(128): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1969+639G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607866 | ||||||
| chr7:2607877
|
T | C | 161 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(158): Show | 162 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.1969+650T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607877 | ||||||
| chr7:2607908
|
C | G | 1 | a0013c0024t0001g0201 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1969+681C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607908 | ||||||
| chr7:2607956
|
G | A | 1 | a0006c0048t0065g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1969+729G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607956 | ||||||
| chr7:2607971
|
C | T | 10 | a0004c0008t0010g0015a0004c0008t0010g0016a0004c0008t0010g0018others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1969+744C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2607971 | ||||||
| chr7:2608100
|
G | A | 1 | a0023c0043t0018g0147 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1969+873G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608100 | ||||||
| chr7:2608136
|
C | A | 8 | a0001c0010t0009g0005a0001c0010t0009g0121a0001c0010t0009g0122others(5): Show | 8 | HG01192.hp2 HG01243.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1969+909C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608136 | ||||||
| chr7:2608166
|
G | A | 42 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(39): Show | 43 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1969+939G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608166 | ||||||
| chr7:2608219
|
G | A | 6 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(3): Show | 6 | HG01496.hp2 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1969+992G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608219 | ||||||
| chr7:2608224
|
GGGCGGAG others(10): Show |
G | 1 | a0024c0042t0074g0059 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1969+998_1969+1014 others(20): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608224 | ||||||
| chr7:2608225
|
G | A | 2 | a0006c0009t0102g0214a0006c0048t0065g0165 | 2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1969+998G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608225 | ||||||
| chr7:2608228
|
G | A | 1 | a0003c0005t0110g0258 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1969+1001G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608228 | ||||||
| chr7:2608266
|
C | T | 2 | a0002c0002t0003g0361a0002c0002t0003g0384 | 2 | HG02165.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1969+1039C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608266 | ||||||
| chr7:2608329
|
C | G | 6 | a0005c0007t0007g0262a0005c0007t0007g0275a0005c0007t0007g0276others(3): Show | 6 | HG00280.hp2 HG00733.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1969+1102C>G | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608329 | ||||||
| chr7:2608396
|
G | A | 1 | a0012c0023t0001g0288 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1969+1169G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608396 | ||||||
| chr7:2608404
|
C | T | 2 | a0001c0001t0005g0175a0001c0001t0005g0178 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1969+1177C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608404 | ||||||
| chr7:2608436
|
C | T | 12 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0055others(9): Show | 12 | HG00621.hp2 HG02074.hp1 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.1969+1209C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608436 | ||||||
| chr7:2608473
|
C | A | 16 | a0005c0007t0007g0002a0005c0007t0007g0067a0005c0007t0007g0101others(13): Show | 16 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.1969+1246C>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608473 | ||||||
| chr7:2608508
|
C | T | 1 | a0002c0004t0012g0294 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1969+1281C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608508 | ||||||
| chr7:2608634
|
G | A | 233 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(230): Show | 235 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.1969+1407G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608634 | ||||||
| chr7:2608852
|
GTT | G | 42 | a0003c0005t0008g0177a0003c0005t0008g0182a0003c0005t0008g0187others(39): Show | 43 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1970-1191_1970-119 others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608852 | ||||||
| chr7:2608964
|
C | T | 163 | a0001c0029t0051g0171a0002c0002t0002g0006a0002c0002t0002g0010others(160): Show | 164 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1970-1080C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2608964 | ||||||
| chr7:2609042
|
C | T | 59 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(56): Show | 59 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1970-1002C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609042 | ||||||
| chr7:2609103
|
C | T | 4 | a0009c0013t0022g0051a0009c0013t0022g0084a0009c0013t0022g0154others(1): Show | 4 | HG02257.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1970-941C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609103 | ||||||
| chr7:2609252
|
C | T | 156 | a0001c0001t0006g0255a0001c0029t0051g0171a0002c0002t0002g0006others(153): Show | 157 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1970-792C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609252 | ||||||
| chr7:2609260
|
G | T | 2 | a0001c0001t0001g0228a0001c0001t0001g0237 | 2 | NA18950.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1970-784G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609260 | ||||||
| chr7:2609276
|
T | C | 203 | a0001c0029t0051g0171a0002c0002t0002g0006a0002c0002t0002g0010others(200): Show | 205 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.1970-768T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609276 | ||||||
| chr7:2609311
|
C | CT | 20 | a0001c0001t0001g0224a0001c0001t0001g0299a0001c0001t0054g0273others(17): Show | 20 | HG00741.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1970-715dupT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr7 | 2609311 | |||||
| chr7:2609311
|
CT | C | 8 | a0001c0001t0001g0228a0001c0003t0001g0333a0004c0008t0010g0022others(5): Show | 8 | HG02145.hp2 HG02897.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1970-715delT | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr7 | 2609311 | |||||
| chr7:2609311
|
CTT | C | 88 | a0002c0002t0002g0006a0002c0002t0002g0029a0002c0002t0002g0049others(85): Show | 90 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.1970-716_1970-715d others(4): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr7 | 2609311 | |||||
| chr7:2609311
|
CTTT | C | 101 | a0001c0029t0051g0171a0002c0002t0002g0010a0002c0002t0002g0033others(98): Show | 101 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1970-717_1970-715d others(5): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr7 | 2609311 | |||||
| chr7:2609311
|
CTTTT | C | 8 | a0002c0002t0002g0035a0005c0007t0007g0002a0005c0007t0007g0067others(5): Show | 8 | HG00733.hp2 HG01070.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1970-718_1970-715d others(6): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr7 | 2609311 | |||||
| chr7:2609311
|
CTTTTT | C | 6 | a0005c0007t0007g0262a0005c0007t0007g0275a0005c0007t0007g0276others(3): Show | 6 | HG00280.hp2 HG00733.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1970-719_1970-715d others(7): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr7 | 2609311 | |||||
| chr7:2609398
|
G | A | 1 | a0019c0051t0081g0128 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1970-646G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609398 | ||||||
| chr7:2609399
|
G | A | 6 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(3): Show | 6 | HG01496.hp2 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1970-645G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609399 | ||||||
| chr7:2609402
|
T | A | 6 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(3): Show | 6 | HG01496.hp2 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1970-642T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609402 | ||||||
| chr7:2609515
|
T | TTTCAGGG others(17): Show |
1 | a0023c0043t0018g0147 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1970-528_1970-505d others(26): Show |
IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr7 | 2609515 | |||||
| chr7:2609630
|
T | C | 294 | a0001c0001t0005g0028a0001c0001t0005g0041a0001c0001t0005g0057others(291): Show | 296 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.1970-414T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609630 | ||||||
| chr7:2609684
|
T | A | 1 | a0001c0029t0051g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1970-360T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609684 | ||||||
| chr7:2609714
|
C | T | 1 | a0001c0047t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1970-330C>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609714 | ||||||
| chr7:2609773
|
G | T | 13 | a0005c0007t0007g0002a0005c0007t0007g0067a0005c0007t0007g0101others(10): Show | 13 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1970-271G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609773 | ||||||
| chr7:2609819
|
T | A | 5 | a0007c0012t0019g0120a0007c0012t0019g0138a0007c0012t0019g0139others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1970-225T>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609819 | ||||||
| chr7:2609931
|
G | A | 1 | a0002c0002t0002g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1970-113G>A | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2609931 | ||||||
| chr7:2610006
|
G | T | 6 | a0001c0003t0027g0271a0001c0003t0027g0272a0001c0003t0027g0325others(3): Show | 6 | HG01496.hp2 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1970-38G>T | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2610006 | ||||||
| chr7:2610039
|
T | C | 203 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0029others(200): Show | 205 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(202): Show |
splice_region_variant&intron_variant | LOW | c.1970-5T>C | IQCE | ENSG00000106012.19 | transcript | ENST00000402050.7 | protein_coding | 21/21 | chr7 | 2610039 |