Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9896 |
|---|---|
| ensemblid | ENSG00000112367.12 |
| hgncid | 16873 |
| symbol | FIG4 |
| name | FIG4 phosphoinositide 5-phosphatase |
| refseq_nuc | NM_014845.6 |
| refseq_prot | NP_055660.1 |
| ensembl_nuc | ENST00000230124.8 |
| ensembl_prot | ENSP00000230124.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 109691296 |
| end | 109825426 |
| strand | + |
| ver | v1.2 |
| region | chr6:109691296-109825426 |
| region5000 | chr6:109686296-109830426 |
| regionname0 | FIG4_chr6_109691296_109825426 |
| regionname5000 | FIG4_chr6_109686296_109830426 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 907 | 190 | 22 | 44 | 97 | 7 | 18 | 81 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002 | 0/0 | 907 | 127 | 66 | 14 | 32 | 3 | 12 | 21 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0003 | 0/0 | 907 | 38 | 0 | 7 | 28 | 0 | 3 | 26 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0004 | 0/0 | 907 | 11 | 0 | 1 | 5 | 0 | 5 | 4 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0005 | 0/0 | 907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0006 | 0/0 | 319 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0007 | 0/0 | 907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0008 | 0/0 | 907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2724 | 114 | 18 | 23 | 60 | 3 | 8 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0002 | 0/0 | 2724 | 83 | 56 | 6 | 16 | 1 | 4 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0003 | 0/0 | 2724 | 74 | 4 | 19 | 37 | 4 | 10 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0004 | 0/0 | 2724 | 38 | 6 | 8 | 14 | 2 | 8 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0005 | 0/0 | 2724 | 31 | 0 | 7 | 23 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0006 | 0/0 | 2724 | 6 | 0 | 0 | 4 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0007 | 0/0 | 2724 | 5 | 0 | 0 | 3 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0008 | 0/0 | 2724 | 5 | 0 | 1 | 1 | 0 | 3 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0009 | 0/0 | 2724 | 3 | 3 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0010 | 0/0 | 2724 | 2 | 0 | 2 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0011 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0012 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0013 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0014 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0015 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0016 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0017 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0018 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| c0019 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 302 | 179 | 9 | 40 | 98 | 7 | 25 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| t0002 | 1/1 | 302 | 129 | 49 | 26 | 38 | 3 | 11 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| t0003 | 0/0 | 302 | 32 | 6 | 0 | 26 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| t0004 | 0/0 | 302 | 26 | 22 | 2 | 0 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| t0005 | 0/0 | 302 | 3 | 3 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| t0006 | 0/0 | 302 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| 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 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2724 | 114 | 18 | 23 | 60 | 3 | 8 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0001c0003 | 0/0 | 2724 | 74 | 4 | 19 | 37 | 4 | 10 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0001c0010 | 0/0 | 2724 | 2 | 0 | 2 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0002 | 0/0 | 2724 | 83 | 56 | 6 | 16 | 1 | 4 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0004 | 0/0 | 2724 | 38 | 6 | 8 | 14 | 2 | 8 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0009 | 0/0 | 2724 | 3 | 3 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0012 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0014 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0015 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0003c0005 | 0/0 | 2724 | 31 | 0 | 7 | 23 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0003c0007 | 0/0 | 2724 | 5 | 0 | 0 | 3 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0003c0017 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0003c0018 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0004c0006 | 0/0 | 2724 | 6 | 0 | 0 | 4 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0004c0008 | 0/0 | 2724 | 5 | 0 | 1 | 1 | 0 | 3 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0005c0019 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0006c0013 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0007c0016 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0008c0011 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/1 | 3025 | 83 | 13 | 23 | 34 | 3 | 8 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0001c0001t0003 | 0/0 | 3025 | 31 | 5 | 0 | 26 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0001c0003t0001 | 0/0 | 3025 | 74 | 4 | 19 | 37 | 4 | 10 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0001c0010t0002 | 0/0 | 3025 | 2 | 0 | 2 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0002t0001 | 0/0 | 3025 | 21 | 0 | 4 | 14 | 1 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0002t0002 | 0/0 | 3025 | 33 | 31 | 0 | 2 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0002t0003 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0002t0004 | 0/0 | 3025 | 25 | 21 | 2 | 0 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0002t0005 | 0/0 | 3025 | 3 | 3 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0004t0001 | 0/0 | 3025 | 37 | 5 | 8 | 14 | 2 | 8 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0004t0004 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0009t0002 | 0/0 | 3025 | 3 | 3 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0012t0001 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0014t0002 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0002c0015t0001 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0003c0005t0001 | 0/0 | 3025 | 31 | 0 | 7 | 23 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0003c0007t0001 | 0/0 | 3025 | 4 | 0 | 0 | 2 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0003c0007t0002 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0003c0017t0001 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0003c0018t0001 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0004c0006t0001 | 0/0 | 3025 | 6 | 0 | 0 | 4 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0004c0008t0002 | 0/0 | 3025 | 5 | 0 | 1 | 1 | 0 | 3 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0005c0019t0006 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0006c0013t0002 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0007c0016t0001 | 0/0 | 3025 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| a0008c0011t0001 | 0/0 | 3025 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | copy fasta | chr6 | 109686296 | 109830426 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0010t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0010t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0009t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0009t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0009t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0012t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0014t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0015t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0007t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0007t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0007t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0007t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0007t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0017t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0018t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0006t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0006t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0006t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0006t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0006t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0006t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0008t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0008t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0008t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0008t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0008t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0005c0019t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0006c0013t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0007c0016t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0008c0011t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0004 | t0001 | g0037 | EUR | GBR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0243 | EUR | GBR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0050 | EUR | FIN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0153 | EUR | FIN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0036 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0265 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00423 | hp2 | a0002 | c0004 | t0001 | g0062 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0358 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00639 | hp1 | a0003 | c0005 | t0001 | g0325 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0283 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0278 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0173 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0259 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0258 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01081 | hp1 | a0002 | c0002 | t0004 | g0356 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0170 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0262 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0282 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01175 | hp2 | a0003 | c0005 | t0001 | g0349 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0079 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01243 | hp2 | a0002 | c0002 | t0004 | g0207 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01255 | hp2 | a0002 | c0004 | t0001 | g0128 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0300 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01258 | hp1 | a0001 | c0010 | t0002 | g0026 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0301 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01261 | hp1 | a0002 | c0004 | t0001 | g0220 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0270 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01346 | hp1 | a0002 | c0004 | t0001 | g0215 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0302 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01358 | hp2 | a0003 | c0005 | t0001 | g0317 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0303 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01361 | hp2 | a0002 | c0004 | t0001 | g0232 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01433 | hp1 | a0002 | c0004 | t0001 | g0174 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0261 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01496 | hp1 | a0004 | c0008 | t0002 | g0315 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01496 | hp2 | a0001 | c0010 | t0002 | g0027 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0272 | EUR | IBS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0273 | EUR | IBS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0304 | EUR | IBS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01928 | hp1 | a0003 | c0005 | t0001 | g0326 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0132 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01934 | hp2 | a0002 | c0004 | t0001 | g0189 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01952 | hp1 | a0003 | c0005 | t0001 | g0316 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01952 | hp2 | a0008 | c0011 | t0001 | g0367 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01975 | hp2 | a0007 | c0016 | t0001 | g0078 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0296 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0177 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0172 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02004 | hp2 | a0003 | c0005 | t0001 | g0312 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02056 | hp1 | a0002 | c0004 | t0001 | g0041 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02071 | hp1 | a0002 | c0004 | t0001 | g0028 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02071 | hp2 | a0004 | c0008 | t0002 | g0310 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0263 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02074 | hp2 | a0003 | c0005 | t0001 | g0329 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02132 | hp1 | a0002 | c0004 | t0001 | g0039 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02132 | hp2 | a0002 | c0012 | t0001 | g0137 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0073 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02148 | hp2 | a0002 | c0004 | t0001 | g0129 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02155 | hp1 | a0002 | c0004 | t0001 | g0040 | EAS | CDX | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02155 | hp2 | a0003 | c0005 | t0001 | g0342 | EAS | CDX | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02257 | hp1 | a0002 | c0002 | t0004 | g0208 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0121 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0281 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02258 | hp2 | a0002 | c0002 | t0004 | g0229 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02280 | hp1 | a0002 | c0002 | t0004 | g0202 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0147 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02300 | hp2 | a0003 | c0005 | t0001 | g0327 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02451 | hp1 | a0002 | c0002 | t0004 | g0200 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02451 | hp2 | a0002 | c0002 | t0004 | g0294 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02523 | hp1 | a0002 | c0004 | t0001 | g0051 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0276 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0083 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02602 | hp1 | a0002 | c0004 | t0001 | g0248 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0285 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0298 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0365 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0366 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0164 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02698 | hp1 | a0002 | c0002 | t0004 | g0186 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02698 | hp2 | a0002 | c0004 | t0001 | g0064 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02717 | hp1 | a0002 | c0002 | t0004 | g0196 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0257 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0043 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02735 | hp2 | a0002 | c0004 | t0001 | g0231 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0024 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02809 | hp1 | a0002 | c0002 | t0004 | g0228 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0364 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0225 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0116 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0085 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02895 | hp1 | a0002 | c0009 | t0002 | g0159 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0362 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02896 | hp2 | a0002 | c0002 | t0004 | g0206 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02897 | hp1 | a0002 | c0009 | t0002 | g0157 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02922 | hp2 | a0002 | c0002 | t0004 | g0360 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02965 | hp1 | a0002 | c0004 | t0001 | g0205 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02965 | hp2 | a0002 | c0002 | t0004 | g0354 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0204 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0114 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0110 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03017 | hp1 | a0003 | c0007 | t0001 | g0328 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03041 | hp1 | a0006 | c0013 | t0002 | g0222 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03041 | hp2 | a0005 | c0019 | t0006 | g0016 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0118 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03098 | hp2 | a0002 | c0002 | t0004 | g0123 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0363 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0277 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0117 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0210 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03209 | hp2 | a0002 | c0002 | t0004 | g0238 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0084 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0112 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03239 | hp1 | a0002 | c0004 | t0001 | g0061 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0351 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03453 | hp1 | a0002 | c0002 | t0005 | g0127 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0012 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03486 | hp1 | a0002 | c0002 | t0004 | g0197 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0115 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0271 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03490 | hp2 | a0002 | c0004 | t0001 | g0089 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03516 | hp1 | a0002 | c0004 | t0001 | g0161 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03516 | hp2 | a0002 | c0002 | t0004 | g0357 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0119 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03579 | hp1 | a0002 | c0004 | t0001 | g0160 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03654 | hp1 | a0002 | c0002 | t0004 | g0352 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03654 | hp2 | a0003 | c0005 | t0001 | g0311 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03704 | hp1 | a0002 | c0004 | t0001 | g0295 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03704 | hp2 | a0003 | c0007 | t0001 | g0313 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0286 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03710 | hp2 | a0002 | c0004 | t0001 | g0072 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0353 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0060 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03834 | hp1 | a0002 | c0004 | t0001 | g0242 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03927 | hp2 | a0004 | c0006 | t0001 | g0308 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0154 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03942 | hp2 | a0004 | c0008 | t0002 | g0323 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0288 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0251 | SAS | STU | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04199 | hp2 | a0004 | c0008 | t0002 | g0309 | SAS | STU | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04204 | hp1 | a0004 | c0008 | t0002 | g0322 | SAS | STU | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0087 | SAS | STU | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | STU | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0031 | SAS | STU | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18522 | hp1 | a0002 | c0002 | t0004 | g0006 | AFR | YRI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0113 | AFR | YRI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | CHB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | CHB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0252 | EAS | CHB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18906 | hp1 | a0002 | c0014 | t0002 | g0011 | AFR | YRI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18906 | hp2 | a0002 | c0002 | t0005 | g0126 | AFR | YRI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18940 | hp2 | a0003 | c0005 | t0001 | g0335 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18943 | hp1 | a0003 | c0005 | t0001 | g0350 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18946 | hp1 | a0002 | c0004 | t0001 | g0053 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18946 | hp2 | a0001 | c0003 | t0001 | g0287 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18947 | hp1 | a0003 | c0005 | t0001 | g0341 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18948 | hp2 | a0003 | c0005 | t0001 | g0250 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0293 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0264 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18952 | hp1 | a0003 | c0005 | t0001 | g0330 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18953 | hp2 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0274 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0275 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18959 | hp2 | a0003 | c0017 | t0001 | g0314 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18960 | hp1 | a0002 | c0004 | t0001 | g0256 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0253 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18961 | hp2 | a0002 | c0004 | t0001 | g0067 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18962 | hp2 | a0004 | c0006 | t0001 | g0307 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18967 | hp1 | a0003 | c0005 | t0001 | g0334 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18968 | hp2 | a0003 | c0005 | t0001 | g0320 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18969 | hp1 | a0001 | c0003 | t0001 | g0319 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18970 | hp1 | a0003 | c0005 | t0001 | g0068 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18973 | hp2 | a0003 | c0005 | t0001 | g0345 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0254 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0297 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18978 | hp1 | a0002 | c0004 | t0001 | g0178 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18978 | hp2 | a0001 | c0003 | t0001 | g0266 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0097 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18982 | hp1 | a0002 | c0004 | t0001 | g0063 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18982 | hp2 | a0003 | c0005 | t0001 | g0332 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0171 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18983 | hp2 | a0003 | c0005 | t0001 | g0002 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18985 | hp1 | a0002 | c0004 | t0001 | g0066 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18986 | hp1 | a0003 | c0007 | t0001 | g0321 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18990 | hp2 | a0001 | c0003 | t0001 | g0188 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0291 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18994 | hp2 | a0003 | c0005 | t0001 | g0343 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18995 | hp1 | a0003 | c0005 | t0001 | g0002 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18999 | hp1 | a0003 | c0005 | t0001 | g0336 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19003 | hp1 | a0003 | c0005 | t0001 | g0333 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0269 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19005 | hp2 | a0003 | c0005 | t0001 | g0249 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19007 | hp2 | a0002 | c0004 | t0001 | g0140 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19010 | hp2 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19012 | hp1 | a0002 | c0015 | t0001 | g0181 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19012 | hp2 | a0004 | c0006 | t0001 | g0306 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19043 | hp1 | a0002 | c0002 | t0005 | g0125 | AFR | LWK | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19043 | hp2 | a0002 | c0002 | t0004 | g0355 | AFR | LWK | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19055 | hp1 | a0002 | c0004 | t0001 | g0131 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19055 | hp2 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19057 | hp1 | a0004 | c0006 | t0001 | g0344 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19063 | hp2 | a0003 | c0005 | t0001 | g0337 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19066 | hp2 | a0003 | c0005 | t0001 | g0340 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19075 | hp1 | a0001 | c0003 | t0001 | g0292 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19079 | hp2 | a0003 | c0005 | t0001 | g0331 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19082 | hp1 | a0003 | c0007 | t0002 | g0348 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19084 | hp2 | a0003 | c0005 | t0001 | g0338 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19085 | hp2 | a0003 | c0018 | t0001 | g0318 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19086 | hp2 | a0003 | c0005 | t0001 | g0346 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0368 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19091 | hp1 | a0004 | c0006 | t0001 | g0339 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0111 | AFR | YRI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19240 | hp2 | a0002 | c0009 | t0002 | g0158 | AFR | YRI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0069 | AFR | ASW | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ASW | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20752 | hp1 | a0002 | c0004 | t0001 | g0216 | EUR | TSI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0260 | EUR | TSI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0152 | SAS | GIH | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20905 | hp2 | a0004 | c0006 | t0001 | g0324 | SAS | GIH | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01123 | hp1 | a0002 | c0004 | t0001 | g0219 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0211 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0280 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02559 | hp2 | a0002 | c0002 | t0004 | g0201 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03471 | hp1 | a0002 | c0004 | t0001 | g0199 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0209 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG06807 | hp1 | a0002 | c0004 | t0001 | g0212 | AFR | USA | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG06807 | hp2 | a0002 | c0004 | t0004 | g0230 | AFR | USA | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18955 | hp1 | a0003 | c0007 | t0001 | g0347 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20300 | hp1 | a0002 | c0002 | t0004 | g0305 | AFR | USA | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20300 | hp2 | a0002 | c0002 | t0004 | g0359 | AFR | USA | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0120 | AFR | LWK | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA21309 | hp2 | a0002 | c0002 | t0004 | g0203 | AFR | LWK | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0239 | REF | REF | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0054 | REF | REF | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:109715133
|
T | C | 1 | a0008 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.122T>C | p.Ile41Thr | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/23 | 262/3025 | 122/2724 | 41/907 | chr6 | 109715133 | ||
| chr6:109741476
|
A | G | 1 | a0005 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.808A>G | p.Thr270Ala | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/23 | 948/3025 | 808/2724 | 270/907 | chr6 | 109741476 | ||
| chr6:109743192
|
C | A | 1 | a0006 | 1 | HG03041.hp1 | stop_gained | HIGH | c.959C>A | p.Ser320* | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 9/23 | 1099/3025 | 959/2724 | 320/907 | chr6 | 109743192 | ||
| chr6:109743725
|
A | T | 2 | a0003a0004 | 49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
missense_variant | MODERATE | c.1090A>T | p.Met364Leu | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/23 | 1230/3025 | 1090/2724 | 364/907 | chr6 | 109743725 | ||
| chr6:109760380
|
A | G | 1 | a0007 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.1268A>G | p.Lys423Arg | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/23 | 1408/3025 | 1268/2724 | 423/907 | chr6 | 109760380 | ||
| chr6:109786314
|
T | C | 3 | a0002a0003a0007 | 166 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(163): Show |
missense_variant | MODERATE | c.1961T>C | p.Val654Ala | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/23 | 2101/3025 | 1961/2724 | 654/907 | chr6 | 109786314 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:109716531
|
G | A | 1 | a0002c0012 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.252G>A | p.Ser84Ser | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/23 | 392/3025 | 252/2724 | 84/907 | chr6 | 109716531 | ||
| chr6:109735199
|
C | A | 1 | a0001c0010 | 2 | HG01258.hp1 HG01496.hp2 |
synonymous_variant | LOW | c.547C>A | p.Arg183Arg | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/23 | 687/3025 | 547/2724 | 183/907 | chr6 | 109735199 | ||
| chr6:109760354
|
T | C | 1 | a0002c0009 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1242T>C | p.Ile414Ile | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/23 | 1382/3025 | 1242/2724 | 414/907 | chr6 | 109760354 | ||
| chr6:109762181
|
C | T | 1 | a0003c0018 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.1362C>T | p.Tyr454Tyr | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/23 | 1502/3025 | 1362/2724 | 454/907 | chr6 | 109762181 | ||
| chr6:109766730
|
T | C | 1 | a0002c0014 | 1 | NA18906.hp1 | splice_region_variant&synonymous_variant | LOW | c.1585T>C | p.Leu529Leu | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/23 | 1725/3025 | 1585/2724 | 529/907 | chr6 | 109766730 | ||
| chr6:109791418
|
G | T | 2 | a0002c0015a0003c0017 | 2 | NA18959.hp2 NA19012.hp1 |
synonymous_variant | LOW | c.2223G>T | p.Thr741Thr | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/23 | 2363/3025 | 2223/2724 | 741/907 | chr6 | 109791418 | ||
| chr6:109825100
|
G | A | 8 | a0001c0003a0002c0004a0002c0015others(5): Show | 153 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(150): Show |
synonymous_variant | LOW | c.2559G>A | p.Ser853Ser | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 23/23 | 2699/3025 | 2559/2724 | 853/907 | chr6 | 109825100 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:109691315
|
G | A | 1 | a0002c0002t0005 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-121G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/23 | 121 | chr6 | 109691315 | |||||
| chr6:109691316
|
C | T | 1 | a0002c0002t0005 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-120C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/23 | 120 | chr6 | 109691316 | |||||
| chr6:109825272
|
C | T | 2 | a0001c0001t0003a0002c0002t0003 | 32 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*7C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 23/23 | 7 | chr6 | 109825272 | |||||
| chr6:109825279
|
C | T | 1 | a0005c0019t0006 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 23/23 | 14 | chr6 | 109825279 | |||||
| chr6:109825294
|
G | A | 2 | a0002c0002t0004a0002c0004t0004 | 26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*29G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 23/23 | 29 | chr6 | 109825294 | |||||
| chr6:109825385
|
C | T | 12 | a0001c0003t0001a0002c0002t0001a0002c0004t0001others(9): Show | 179 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*120C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 23/23 | 120 | chr6 | 109825385 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:109691550
|
C | T | 1 | a0001c0003t0001g0368 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.66+49C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109691550 | ||||||
| chr6:109691626
|
A | G | 1 | a0008c0011t0001g0367 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.66+125A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109691626 | ||||||
| chr6:109691974
|
T | C | 2 | a0001c0003t0001g0003a0001c0003t0001g0004 | 2 | NA18943.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.66+473T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109691974 | ||||||
| chr6:109692033
|
A | G | 3 | a0001c0001t0003g0364a0001c0001t0003g0365a0001c0001t0003g0366 | 3 | HG02615.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.66+532A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109692033 | ||||||
| chr6:109692163
|
G | C | 4 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0002g0008others(1): Show | 4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+662G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109692163 | ||||||
| chr6:109692307
|
A | T | 2 | a0002c0002t0002g0362a0002c0002t0002g0363 | 2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.66+806A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109692307 | ||||||
| chr6:109692708
|
T | TC | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+1210dupC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109692708 | |||||
| chr6:109692744
|
C | T | 1 | a0001c0001t0002g0361 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.66+1243C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109692744 | ||||||
| chr6:109692963
|
C | T | 2 | a0002c0002t0004g0359a0002c0002t0004g0360 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.66+1462C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109692963 | ||||||
| chr6:109693031
|
A | G | 1 | a0002c0002t0001g0358 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.66+1530A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693031 | ||||||
| chr6:109693039
|
G | A | 1 | a0001c0003t0001g0014 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.66+1538G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693039 | ||||||
| chr6:109693145
|
T | TG | 271 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(268): Show | 273 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.66+1646dupG | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109693145 | |||||
| chr6:109693190
|
G | C | 12 | a0002c0002t0002g0110a0002c0002t0002g0111a0002c0002t0002g0112others(9): Show | 12 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.66+1689G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693190 | ||||||
| chr6:109693277
|
G | A | 3 | a0001c0001t0003g0364a0001c0001t0003g0365a0001c0001t0003g0366 | 3 | HG02615.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.66+1776G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693277 | ||||||
| chr6:109693478
|
G | A | 3 | a0001c0001t0002g0122a0001c0001t0002g0124a0002c0002t0004g0123 | 3 | HG02622.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.66+1977G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693478 | ||||||
| chr6:109693492
|
C | G | 2 | a0002c0002t0002g0012a0002c0002t0002g0013 | 2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.66+1991C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693492 | ||||||
| chr6:109693679
|
C | T | 271 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(268): Show | 273 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.66+2178C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693679 | ||||||
| chr6:109693704
|
C | A | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+2203C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693704 | ||||||
| chr6:109693890
|
A | G | 118 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(115): Show | 119 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(116): Show |
intron_variant | MODIFIER | c.66+2389A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693890 | ||||||
| chr6:109693898
|
GGTTTT | G | 104 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(101): Show | 105 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.66+2418_66+2422del others(5): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109693898 | |||||
| chr6:109693898
|
GGTTTTGT others(3): Show |
G | 4 | a0001c0001t0003g0244a0001c0001t0003g0245a0001c0001t0003g0246others(1): Show | 4 | NA18939.hp1 NA18940.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+2413_66+2422del others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109693898 | |||||
| chr6:109693998
|
T | TA | 45 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(42): Show | 45 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.66+2504dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109693998 | |||||
| chr6:109694006
|
CAA | C | 9 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(6): Show | 9 | HG02280.hp2 HG02559.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+2509_66+2510del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109694006 | |||||
| chr6:109694052
|
T | G | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+2551T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694052 | ||||||
| chr6:109694120
|
A | G | 103 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(100): Show | 104 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.66+2619A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694120 | ||||||
| chr6:109694361
|
T | C | 3 | a0001c0003t0001g0291a0001c0003t0001g0292a0001c0003t0001g0293 | 3 | NA18949.hp2 NA18994.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.66+2860T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694361 | ||||||
| chr6:109694458
|
G | A | 3 | a0001c0001t0002g0015a0001c0001t0002g0017a0005c0019t0006g0016 | 3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.66+2957G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694458 | ||||||
| chr6:109694672
|
T | C | 118 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(115): Show | 119 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(116): Show |
intron_variant | MODIFIER | c.66+3171T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694672 | ||||||
| chr6:109694828
|
T | C | 1 | a0002c0004t0001g0248 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.66+3327T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694828 | ||||||
| chr6:109694943
|
C | A | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+3442C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694943 | ||||||
| chr6:109695409
|
T | C | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+3908T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695409 | ||||||
| chr6:109695453
|
A | G | 31 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0217others(28): Show | 31 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.66+3952A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695453 | ||||||
| chr6:109695458
|
G | A | 1 | a0002c0002t0001g0358 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.66+3957G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695458 | ||||||
| chr6:109695527
|
G | A | 9 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(6): Show | 9 | HG02280.hp2 HG02559.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+4026G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695527 | ||||||
| chr6:109695560
|
A | G | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+4059A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695560 | ||||||
| chr6:109695579
|
T | TAC | 97 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(94): Show | 98 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.66+4098_66+4099dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695579 | |||||
| chr6:109695579
|
T | TACAC | 30 | a0001c0003t0001g0319a0001c0003t0001g0368a0002c0004t0001g0161others(27): Show | 31 | HG00639.hp1 HG01358.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.66+4096_66+4099dup others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695579 | |||||
| chr6:109695579
|
T | TACACACA others(19): Show |
1 | a0002c0004t0001g0129 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.66+4099_66+4100ins others(26): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695579 | |||||
| chr6:109695579
|
TAC | T | 13 | a0002c0002t0002g0110a0002c0002t0002g0111a0002c0002t0002g0112others(10): Show | 13 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.66+4098_66+4099del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695579 | |||||
| chr6:109695581
|
C | CACACACA others(15): Show |
2 | a0002c0002t0001g0153a0002c0002t0001g0154 | 2 | HG00323.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.66+4099_66+4100ins others(22): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695581 | |||||
| chr6:109695583
|
C | CACACACA others(15): Show |
2 | a0002c0002t0001g0358a0002c0004t0001g0128 | 2 | HG00544.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.66+4099_66+4100ins others(22): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695583 | |||||
| chr6:109695583
|
C | CACACACA others(13): Show |
23 | a0001c0003t0001g0145a0002c0002t0001g0130a0002c0002t0001g0132others(20): Show | 23 | HG01934.hp1 HG01943.hp1 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.66+4099_66+4100ins others(20): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695583 | |||||
| chr6:109695587
|
C | CACACACA others(9): Show |
1 | a0001c0001t0003g0366 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.66+4099_66+4100ins others(16): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695587 | |||||
| chr6:109695589
|
C | CACACACA others(7): Show |
2 | a0001c0001t0003g0364a0001c0001t0003g0365 | 2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.66+4099_66+4100ins others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695589 | |||||
| chr6:109695595
|
C | CACACACA others(3): Show |
1 | a0003c0005t0001g0349 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.66+4099_66+4100ins others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695595 | |||||
| chr6:109695599
|
C | CACACACA others(3): Show |
1 | a0004c0006t0001g0306 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.66+4099_66+4100ins others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695599 | |||||
| chr6:109695599
|
C | CACACAG | 17 | a0003c0005t0001g0332a0003c0005t0001g0333a0003c0005t0001g0334others(14): Show | 17 | HG02155.hp2 NA18940.hp2 NA18947.hp1 others(14): Show |
intron_variant | MODIFIER | c.66+4099_66+4100ins others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695599 | |||||
| chr6:109695601
|
G | C | 53 | a0001c0001t0003g0364a0001c0001t0003g0365a0001c0001t0003g0366others(50): Show | 53 | HG00323.hp2 HG00544.hp2 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.66+4100G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695601 | ||||||
| chr6:109695601
|
G | GAC | 9 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(6): Show | 9 | HG03453.hp1 NA18906.hp2 NA18967.hp2 others(6): Show |
intron_variant | MODIFIER | c.66+4122_66+4123dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695601 | |||||
| chr6:109695601
|
G | GACACACA others(5): Show |
2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.66+4112_66+4123dup others(12): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695601 | |||||
| chr6:109695601
|
GAC | G | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0003t0001g0020 | 3 | HG00544.hp1 NA18612.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.66+4122_66+4123del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695601 | |||||
| chr6:109695653
|
G | A | 1 | a0001c0001t0003g0162 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.66+4152G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695653 | ||||||
| chr6:109695680
|
C | G | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.66+4179C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695680 | ||||||
| chr6:109695705
|
G | A | 271 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(268): Show | 273 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.66+4204G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695705 | ||||||
| chr6:109695880
|
A | G | 1 | a0001c0001t0002g0290 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.66+4379A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695880 | ||||||
| chr6:109696356
|
T | G | 1 | a0001c0003t0001g0021 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.66+4855T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696356 | ||||||
| chr6:109696359
|
G | A | 1 | a0001c0001t0003g0022 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.66+4858G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696359 | ||||||
| chr6:109696392
|
A | G | 238 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(235): Show | 240 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(237): Show |
intron_variant | MODIFIER | c.66+4891A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696392 | ||||||
| chr6:109696397
|
C | T | 1 | a0002c0002t0004g0357 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.66+4896C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696397 | ||||||
| chr6:109696432
|
A | G | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.66+4931A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696432 | ||||||
| chr6:109696464
|
G | A | 1 | a0002c0004t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.66+4963G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696464 | ||||||
| chr6:109696683
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.66+5182C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696683 | ||||||
| chr6:109696696
|
A | G | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+5195A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696696 | ||||||
| chr6:109696701
|
A | G | 2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.66+5200A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696701 | ||||||
| chr6:109696974
|
C | T | 1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.66+5473C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696974 | ||||||
| chr6:109697128
|
G | C | 1 | a0002c0002t0001g0130 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.66+5627G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697128 | ||||||
| chr6:109697146
|
T | C | 271 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(268): Show | 273 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.66+5645T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697146 | ||||||
| chr6:109697261
|
C | CA | 30 | a0001c0001t0002g0015a0001c0001t0002g0018a0001c0001t0002g0104others(27): Show | 30 | HG00544.hp1 HG00735.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.66+5778dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109697261 | |||||
| chr6:109697261
|
C | CAA | 6 | a0001c0003t0001g0296a0002c0004t0001g0295a0002c0009t0002g0157others(3): Show | 6 | HG01978.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+5777_66+5778dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109697261 | |||||
| chr6:109697270
|
A | G | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+5769A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697270 | ||||||
| chr6:109697360
|
G | A | 1 | a0002c0004t0001g0248 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.66+5859G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697360 | ||||||
| chr6:109697391
|
T | C | 4 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0002g0008others(1): Show | 4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+5890T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697391 | ||||||
| chr6:109697394
|
A | G | 2 | a0001c0001t0002g0103a0008c0011t0001g0367 | 2 | HG00741.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.66+5893A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697394 | ||||||
| chr6:109697661
|
C | T | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.66+6160C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697661 | ||||||
| chr6:109697704
|
A | G | 1 | a0001c0003t0001g0243 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.66+6203A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697704 | ||||||
| chr6:109697889
|
AT | A | 183 | a0001c0001t0002g0025a0001c0001t0002g0198a0001c0001t0002g0213others(180): Show | 184 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(181): Show |
intron_variant | MODIFIER | c.66+6403delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109697889 | |||||
| chr6:109697889
|
ATT | A | 53 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0003g0001others(50): Show | 54 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.66+6402_66+6403del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109697889 | |||||
| chr6:109697951
|
C | A | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+6450C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697951 | ||||||
| chr6:109698130
|
C | T | 4 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127others(1): Show | 4 | HG03453.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+6629C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698130 | ||||||
| chr6:109698189
|
G | GT | 45 | a0001c0001t0002g0102a0001c0001t0003g0155a0001c0001t0003g0156others(42): Show | 45 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.66+6700dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109698189 | |||||
| chr6:109698201
|
T | A | 2 | a0002c0002t0004g0359a0002c0002t0004g0360 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.66+6700T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698201 | ||||||
| chr6:109698405
|
T | A | 2 | a0001c0010t0002g0026a0001c0010t0002g0027 | 2 | HG01258.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.66+6904T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698405 | ||||||
| chr6:109698432
|
T | C | 1 | a0005c0019t0006g0016 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.66+6931T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698432 | ||||||
| chr6:109698503
|
T | C | 5 | a0001c0001t0002g0255a0001c0003t0001g0252a0001c0003t0001g0253others(2): Show | 5 | HG02004.hp1 NA18747.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+7002T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698503 | ||||||
| chr6:109698509
|
A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.66+7008A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698509 | ||||||
| chr6:109698567
|
C | T | 2 | a0002c0002t0001g0152a0002c0002t0001g0154 | 2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.66+7066C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698567 | ||||||
| chr6:109698699
|
A | G | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+7198A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698699 | ||||||
| chr6:109698708
|
G | A | 4 | a0001c0001t0002g0198a0002c0002t0004g0196a0002c0002t0004g0197others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+7207G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698708 | ||||||
| chr6:109698764
|
A | C | 19 | a0001c0001t0002g0025a0001c0001t0002g0090a0001c0001t0002g0091others(16): Show | 19 | HG00423.hp1 NA18747.hp1 NA18953.hp1 others(16): Show |
intron_variant | MODIFIER | c.66+7263A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698764 | ||||||
| chr6:109698769
|
C | T | 3 | a0003c0005t0001g0329a0003c0005t0001g0330a0003c0005t0001g0331 | 3 | HG02074.hp2 NA18952.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.66+7268C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698769 | ||||||
| chr6:109698799
|
T | C | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.66+7298T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698799 | ||||||
| chr6:109699122
|
A | G | 1 | a0002c0002t0003g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.66+7621A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699122 | ||||||
| chr6:109699169
|
T | C | 1 | a0002c0004t0001g0028 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.66+7668T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699169 | ||||||
| chr6:109699460
|
G | A | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+7959G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699460 | ||||||
| chr6:109699480
|
C | T | 1 | a0002c0004t0001g0242 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.66+7979C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699480 | ||||||
| chr6:109699498
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0002g0351 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.66+8005_66+8019del others(15): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109699498 | |||||
| chr6:109699499
|
T | G | 1 | a0001c0001t0002g0106 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.66+7998T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699499 | ||||||
| chr6:109699525
|
C | T | 1 | a0003c0007t0002g0348 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.66+8024C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699525 | ||||||
| chr6:109699526
|
G | A | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+8025G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699526 | ||||||
| chr6:109699571
|
C | T | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+8070C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699571 | ||||||
| chr6:109699580
|
G | A | 3 | a0001c0003t0001g0257a0001c0003t0001g0258a0001c0003t0001g0259 | 3 | HG01069.hp2 HG01071.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.66+8079G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699580 | ||||||
| chr6:109699590
|
C | T | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+8089C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699590 | ||||||
| chr6:109699605
|
T | C | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+8104T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699605 | ||||||
| chr6:109699684
|
G | A | 1 | a0004c0008t0002g0310 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.66+8183G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699684 | ||||||
| chr6:109699720
|
T | C | 3 | a0002c0002t0004g0200a0002c0002t0004g0201a0002c0002t0004g0202 | 3 | HG02280.hp1 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.66+8219T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699720 | ||||||
| chr6:109699808
|
A | T | 1 | a0005c0019t0006g0016 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.66+8307A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699808 | ||||||
| chr6:109699811
|
T | C | 1 | a0001c0001t0003g0023 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.66+8310T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699811 | ||||||
| chr6:109699902
|
G | A | 1 | a0002c0004t0001g0215 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.66+8401G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699902 | ||||||
| chr6:109700114
|
T | C | 238 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(235): Show | 240 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(237): Show |
intron_variant | MODIFIER | c.66+8613T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700114 | ||||||
| chr6:109700162
|
A | C | 1 | a0002c0004t0001g0199 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.66+8661A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700162 | ||||||
| chr6:109700242
|
A | G | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+8741A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700242 | ||||||
| chr6:109700272
|
T | G | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+8771T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700272 | ||||||
| chr6:109700320
|
A | G | 1 | a0002c0004t0001g0089 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.66+8819A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700320 | ||||||
| chr6:109700407
|
C | T | 2 | a0001c0001t0002g0088a0001c0003t0001g0087 | 2 | HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.66+8906C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700407 | ||||||
| chr6:109700737
|
G | A | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+9236G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700737 | ||||||
| chr6:109701043
|
A | G | 1 | a0002c0002t0004g0208 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.66+9542A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701043 | ||||||
| chr6:109701099
|
G | A | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+9598G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701099 | ||||||
| chr6:109701209
|
C | T | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.66+9708C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701209 | ||||||
| chr6:109701265
|
A | G | 2 | a0001c0001t0003g0194a0001c0001t0003g0195 | 2 | NA18990.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.66+9764A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701265 | ||||||
| chr6:109701496
|
A | G | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+9995A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701496 | ||||||
| chr6:109701793
|
TG | T | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+10293delG | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701793 | ||||||
| chr6:109701827
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.66+10326G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701827 | ||||||
| chr6:109701947
|
C | A | 4 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(1): Show | 4 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+10446C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701947 | ||||||
| chr6:109701955
|
T | A | 1 | a0001c0003t0001g0014 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.66+10454T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701955 | ||||||
| chr6:109702006
|
G | A | 1 | a0002c0002t0004g0200 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.66+10505G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702006 | ||||||
| chr6:109702019
|
A | G | 2 | a0002c0002t0002g0009a0002c0002t0002g0010 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.66+10518A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702019 | ||||||
| chr6:109702119
|
T | C | 3 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0262 | 3 | HG01099.hp1 HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.66+10618T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702119 | ||||||
| chr6:109702470
|
C | T | 278 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0122others(275): Show | 280 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.66+10969C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702470 | ||||||
| chr6:109702628
|
A | G | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+11127A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702628 | ||||||
| chr6:109702672
|
A | ATTC | 278 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0122others(275): Show | 280 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.66+11174_66+11176d others(5): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109702672 | |||||
| chr6:109702814
|
C | T | 3 | a0001c0001t0003g0364a0001c0001t0003g0365a0001c0001t0003g0366 | 3 | HG02615.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.66+11313C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702814 | ||||||
| chr6:109702908
|
G | C | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.66+11407G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702908 | ||||||
| chr6:109702914
|
A | G | 1 | a0003c0007t0001g0328 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.66+11413A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702914 | ||||||
| chr6:109702973
|
T | C | 4 | a0001c0001t0002g0351a0001c0001t0002g0353a0002c0002t0004g0352others(1): Show | 4 | HG02965.hp2 HG03239.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+11472T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702973 | ||||||
| chr6:109703099
|
A | AT | 103 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(100): Show | 104 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.66+11608dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109703099 | |||||
| chr6:109703113
|
C | A | 49 | a0001c0003t0001g0319a0001c0003t0001g0368a0003c0005t0001g0002others(46): Show | 50 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(47): Show |
intron_variant | MODIFIER | c.66+11612C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703113 | ||||||
| chr6:109703263
|
A | G | 49 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(46): Show | 49 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.66+11762A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703263 | ||||||
| chr6:109703618
|
T | A | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67-11460T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703618 | ||||||
| chr6:109703725
|
A | G | 1 | a0001c0001t0002g0101 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.67-11353A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703725 | ||||||
| chr6:109703752
|
C | T | 1 | a0001c0001t0002g0241 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.67-11326C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703752 | ||||||
| chr6:109703755
|
T | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-11323T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703755 | ||||||
| chr6:109703756
|
C | A | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-11322C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703756 | ||||||
| chr6:109703759
|
T | C | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-11319T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703759 | ||||||
| chr6:109704415
|
G | A | 9 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(6): Show | 9 | HG02280.hp2 HG02559.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-10663G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704415 | ||||||
| chr6:109704476
|
C | G | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-10602C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704476 | ||||||
| chr6:109704651
|
G | C | 59 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0003g0001others(56): Show | 60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-10427G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704651 | ||||||
| chr6:109704675
|
C | CA | 8 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(5): Show | 8 | HG00544.hp1 HG01106.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-10380dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109704675 | |||||
| chr6:109704675
|
CA | C | 216 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0100others(213): Show | 218 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.67-10380delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109704675 | |||||
| chr6:109704675
|
CAA | C | 16 | a0001c0001t0002g0240a0001c0001t0003g0190a0001c0003t0001g0259others(13): Show | 16 | HG00639.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.67-10381_67-10380d others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109704675 | |||||
| chr6:109704702
|
G | A | 4 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0002g0008others(1): Show | 4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-10376G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704702 | ||||||
| chr6:109704759
|
A | T | 3 | a0003c0005t0001g0325a0003c0005t0001g0326a0003c0005t0001g0327 | 3 | HG00639.hp1 HG01928.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.67-10319A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704759 | ||||||
| chr6:109704760
|
A | T | 3 | a0003c0005t0001g0325a0003c0005t0001g0326a0003c0005t0001g0327 | 3 | HG00639.hp1 HG01928.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.67-10318A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704760 | ||||||
| chr6:109704776
|
G | A | 1 | a0002c0002t0002g0110 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.67-10302G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704776 | ||||||
| chr6:109705156
|
G | A | 7 | a0001c0001t0002g0351a0001c0001t0002g0353a0002c0002t0004g0352others(4): Show | 7 | HG01081.hp1 HG02965.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-9922G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705156 | ||||||
| chr6:109705369
|
C | T | 1 | a0002c0002t0002g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67-9709C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705369 | ||||||
| chr6:109705394
|
G | T | 2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67-9684G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705394 | ||||||
| chr6:109705456
|
T | C | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67-9622T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705456 | ||||||
| chr6:109705657
|
A | G | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-9421A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705657 | ||||||
| chr6:109705769
|
A | G | 1 | a0002c0002t0004g0200 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67-9309A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705769 | ||||||
| chr6:109705865
|
A | G | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-9213A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705865 | ||||||
| chr6:109705950
|
T | C | 4 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127others(1): Show | 4 | HG03453.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-9128T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705950 | ||||||
| chr6:109706059
|
T | C | 271 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(268): Show | 273 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.67-9019T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706059 | ||||||
| chr6:109706088
|
A | G | 10 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0076others(7): Show | 10 | HG01243.hp1 HG01258.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-8990A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706088 | ||||||
| chr6:109706464
|
T | A | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.67-8614T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706464 | ||||||
| chr6:109706482
|
C | T | 1 | a0002c0004t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.67-8596C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706482 | ||||||
| chr6:109706514
|
G | A | 118 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(115): Show | 119 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(116): Show |
intron_variant | MODIFIER | c.67-8564G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706514 | ||||||
| chr6:109706632
|
C | T | 1 | a0002c0004t0001g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.67-8446C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706632 | ||||||
| chr6:109706740
|
G | T | 118 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(115): Show | 119 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(116): Show |
intron_variant | MODIFIER | c.67-8338G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706740 | ||||||
| chr6:109706873
|
G | C | 49 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(46): Show | 49 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.67-8205G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706873 | ||||||
| chr6:109706902
|
C | T | 278 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0122others(275): Show | 280 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.67-8176C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706902 | ||||||
| chr6:109707108
|
A | T | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.67-7970A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707108 | ||||||
| chr6:109707154
|
T | A | 68 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0003g0001others(65): Show | 69 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.67-7924T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707154 | ||||||
| chr6:109707281
|
A | G | 59 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0003g0001others(56): Show | 60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-7797A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707281 | ||||||
| chr6:109707289
|
A | ATG | 14 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0002g0008others(11): Show | 14 | HG01081.hp1 HG02280.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-7788_67-7787ins others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707289 | |||||
| chr6:109707291
|
A | ATATG | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.67-7786_67-7785ins others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707291 | |||||
| chr6:109707291
|
A | ATG | 14 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(11): Show | 14 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.67-7771_67-7770dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707291 | |||||
| chr6:109707291
|
A | ATGTG | 58 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0003g0001others(55): Show | 59 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.67-7773_67-7770dup others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707291 | |||||
| chr6:109707291
|
A | ATGTGTG | 34 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(31): Show | 34 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.67-7775_67-7770dup others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707291 | |||||
| chr6:109707291
|
A | G | 112 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(109): Show | 113 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(110): Show |
intron_variant | MODIFIER | c.67-7787A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707291 | ||||||
| chr6:109707293
|
G | A | 49 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(46): Show | 49 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.67-7785G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707293 | ||||||
| chr6:109707331
|
G | GTA | 59 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0003g0001others(56): Show | 60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-7738_67-7737dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707331 | |||||
| chr6:109707346
|
T | C | 5 | a0001c0003t0001g0263a0001c0003t0001g0264a0001c0003t0001g0265others(2): Show | 5 | HG00408.hp2 HG02074.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-7732T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707346 | ||||||
| chr6:109707362
|
CGT | C | 227 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(224): Show | 229 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.67-7713_67-7712del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707362 | |||||
| chr6:109707363
|
GTGTA | G | 39 | a0001c0001t0002g0267a0001c0001t0002g0268a0001c0001t0003g0155others(36): Show | 39 | HG00323.hp2 HG00544.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.67-7713_67-7710del others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707363 | |||||
| chr6:109707365
|
G | A | 3 | a0002c0002t0002g0210a0002c0002t0004g0203a0002c0002t0004g0204 | 3 | HG02970.hp1 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.67-7713G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707365 | ||||||
| chr6:109707372
|
T | TATACATA others(21): Show |
2 | a0002c0002t0004g0203a0002c0002t0004g0204 | 2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.67-7703_67-7702ins others(28): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707372 | |||||
| chr6:109707387
|
A | C | 2 | a0002c0002t0004g0203a0002c0002t0004g0204 | 2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.67-7691A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707387 | ||||||
| chr6:109707410
|
T | C | 13 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(10): Show | 13 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.67-7668T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707410 | ||||||
| chr6:109707538
|
G | A | 1 | a0002c0002t0004g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.67-7540G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707538 | ||||||
| chr6:109707578
|
C | T | 4 | a0004c0006t0001g0324a0004c0008t0002g0309a0004c0008t0002g0322others(1): Show | 4 | HG03942.hp2 HG04199.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-7500C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707578 | ||||||
| chr6:109707610
|
T | C | 278 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0122others(275): Show | 280 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.67-7468T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707610 | ||||||
| chr6:109707721
|
T | A | 1 | a0001c0003t0001g0031 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.67-7357T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707721 | ||||||
| chr6:109707759
|
G | A | 59 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0003g0001others(56): Show | 60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-7319G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707759 | ||||||
| chr6:109707763
|
A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-7315A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707763 | ||||||
| chr6:109707817
|
A | T | 1 | a0002c0014t0002g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.67-7261A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707817 | ||||||
| chr6:109707992
|
C | CT | 50 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(47): Show | 50 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.67-7072dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707992 | |||||
| chr6:109708281
|
C | T | 2 | a0001c0001t0002g0214a0001c0001t0002g0239 | 2 | HG01109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.67-6797C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109708281 | ||||||
| chr6:109708439
|
G | T | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-6639G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109708439 | ||||||
| chr6:109708527
|
C | T | 54 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(51): Show | 54 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.67-6551C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109708527 | ||||||
| chr6:109708822
|
G | A | 4 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0002g0008others(1): Show | 4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-6256G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109708822 | ||||||
| chr6:109708858
|
A | G | 1 | a0003c0007t0001g0321 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.67-6220A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109708858 | ||||||
| chr6:109708880
|
C | A | 271 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(268): Show | 273 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.67-6198C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109708880 | ||||||
| chr6:109709225
|
T | C | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.67-5853T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109709225 | ||||||
| chr6:109709314
|
G | A | 1 | a0003c0005t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.67-5764G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109709314 | ||||||
| chr6:109709376
|
A | G | 59 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0003g0001others(56): Show | 60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-5702A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109709376 | ||||||
| chr6:109709769
|
G | T | 12 | a0002c0002t0002g0110a0002c0002t0002g0111a0002c0002t0002g0112others(9): Show | 12 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.67-5309G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109709769 | ||||||
| chr6:109709887
|
G | T | 2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67-5191G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109709887 | ||||||
| chr6:109710007
|
G | A | 2 | a0002c0002t0002g0210a0002c0004t0001g0212 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.67-5071G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710007 | ||||||
| chr6:109710074
|
T | G | 1 | a0001c0003t0001g0291 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.67-5004T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710074 | ||||||
| chr6:109710079
|
T | C | 1 | a0001c0003t0001g0024 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.67-4999T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710079 | ||||||
| chr6:109710118
|
A | T | 271 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(268): Show | 273 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.67-4960A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710118 | ||||||
| chr6:109710382
|
T | C | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-4696T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710382 | ||||||
| chr6:109710571
|
A | G | 1 | a0001c0001t0002g0241 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.67-4507A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710571 | ||||||
| chr6:109710709
|
C | T | 2 | a0001c0001t0002g0070a0001c0001t0002g0071 | 2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.67-4369C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710709 | ||||||
| chr6:109710742
|
C | A | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-4336C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710742 | ||||||
| chr6:109710744
|
A | T | 3 | a0001c0003t0001g0281a0001c0003t0001g0282a0001c0003t0001g0283 | 3 | HG00735.hp2 HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.67-4334A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710744 | ||||||
| chr6:109710909
|
T | TC | 57 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(54): Show | 57 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.67-4169_67-4168ins others(1): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710909 | ||||||
| chr6:109710909
|
T | TCA | 60 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(57): Show | 60 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-4169_67-4168ins others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710909 | ||||||
| chr6:109710909
|
TA | T | 16 | a0002c0002t0001g0130a0002c0002t0001g0149a0002c0002t0002g0110others(13): Show | 16 | HG01943.hp1 HG01952.hp2 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.67-4157delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109710909 | |||||
| chr6:109710910
|
A | C | 138 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(135): Show | 139 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.67-4168A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710910 | ||||||
| chr6:109710910
|
A | T | 4 | a0001c0001t0002g0015a0001c0001t0002g0017a0002c0002t0002g0069others(1): Show | 4 | HG02145.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-4168A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710910 | ||||||
| chr6:109710911
|
A | C | 15 | a0002c0002t0001g0130a0002c0002t0001g0149a0002c0002t0002g0110others(12): Show | 15 | HG01943.hp1 HG02135.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-4167A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710911 | ||||||
| chr6:109711025
|
G | C | 49 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(46): Show | 49 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.67-4053G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711025 | ||||||
| chr6:109711154
|
C | T | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67-3924C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711154 | ||||||
| chr6:109711201
|
C | T | 49 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(46): Show | 49 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.67-3877C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711201 | ||||||
| chr6:109711227
|
G | A | 1 | a0001c0003t0001g0269 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.67-3851G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711227 | ||||||
| chr6:109711263
|
G | A | 1 | a0001c0003t0001g0284 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.67-3815G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711263 | ||||||
| chr6:109711377
|
C | T | 153 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(150): Show | 154 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.67-3701C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711377 | ||||||
| chr6:109711385
|
C | G | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67-3693C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711385 | ||||||
| chr6:109711786
|
G | A | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-3292G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711786 | ||||||
| chr6:109711833
|
T | C | 1 | a0001c0003t0001g0297 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.67-3245T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711833 | ||||||
| chr6:109712045
|
G | C | 4 | a0004c0006t0001g0324a0004c0008t0002g0309a0004c0008t0002g0322others(1): Show | 4 | HG03942.hp2 HG04199.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-3033G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712045 | ||||||
| chr6:109712088
|
T | C | 2 | a0001c0001t0002g0299a0002c0002t0002g0298 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.67-2990T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712088 | ||||||
| chr6:109712246
|
C | G | 3 | a0001c0001t0002g0015a0001c0001t0002g0017a0005c0019t0006g0016 | 3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.67-2832C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712246 | ||||||
| chr6:109712391
|
G | A | 1 | a0001c0003t0001g0262 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.67-2687G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712391 | ||||||
| chr6:109712525
|
G | C | 50 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(47): Show | 50 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.67-2553G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712525 | ||||||
| chr6:109712705
|
A | G | 1 | a0001c0003t0001g0243 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.67-2373A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712705 | ||||||
| chr6:109712824
|
C | T | 1 | a0002c0004t0001g0089 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.67-2254C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712824 | ||||||
| chr6:109713052
|
C | T | 49 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(46): Show | 49 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.67-2026C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713052 | ||||||
| chr6:109713188
|
G | A | 54 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(51): Show | 54 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.67-1890G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713188 | ||||||
| chr6:109713208
|
G | A | 2 | a0002c0004t0001g0215a0002c0004t0001g0216 | 2 | HG01346.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.67-1870G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713208 | ||||||
| chr6:109713225
|
C | T | 14 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(11): Show | 14 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.67-1853C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713225 | ||||||
| chr6:109713292
|
G | T | 2 | a0001c0001t0003g0194a0001c0001t0003g0195 | 2 | NA18990.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.67-1786G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713292 | ||||||
| chr6:109713636
|
C | T | 50 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(47): Show | 50 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.67-1442C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713636 | ||||||
| chr6:109713752
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.67-1326G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713752 | ||||||
| chr6:109713795
|
C | T | 59 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0003g0001others(56): Show | 60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-1283C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713795 | ||||||
| chr6:109713855
|
G | T | 1 | a0002c0004t0001g0129 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.67-1223G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713855 | ||||||
| chr6:109713947
|
C | T | 1 | a0002c0002t0004g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.67-1131C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713947 | ||||||
| chr6:109714045
|
C | A | 1 | a0002c0002t0002g0362 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.67-1033C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109714045 | ||||||
| chr6:109714089
|
G | T | 1 | a0002c0002t0002g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.67-989G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109714089 | ||||||
| chr6:109714522
|
A | G | 2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67-556A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109714522 | ||||||
| chr6:109714672
|
T | C | 59 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0003g0001others(56): Show | 60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-406T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109714672 | ||||||
| chr6:109714709
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.67-369C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109714709 | ||||||
| chr6:109714913
|
T | C | 59 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0003g0001others(56): Show | 60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-165T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109714913 | ||||||
| chr6:109715071
|
T | C | 14 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(11): Show | 14 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.67-7T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109715071 | ||||||
| chr6:109715276
|
A | T | 48 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(45): Show | 48 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.165+100A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | chr6 | 109715276 | ||||||
| chr6:109715404
|
C | T | 4 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159others(1): Show | 4 | HG02071.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+228C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | chr6 | 109715404 | ||||||
| chr6:109715426
|
GAT | G | 17 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0090others(14): Show | 17 | NA18747.hp1 NA18953.hp1 NA18967.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+252_165+253del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 109715426 | |||||
| chr6:109715504
|
C | T | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.165+328C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | chr6 | 109715504 | ||||||
| chr6:109715560
|
C | A | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.165+384C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | chr6 | 109715560 | ||||||
| chr6:109715860
|
G | A | 1 | a0002c0002t0003g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.166-585G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | chr6 | 109715860 | ||||||
| chr6:109716196
|
A | C | 1 | a0001c0001t0002g0096 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.166-249A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | chr6 | 109716196 | ||||||
| chr6:109716719
|
A | G | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.289+151A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109716719 | ||||||
| chr6:109716848
|
A | G | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.289+280A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109716848 | ||||||
| chr6:109716899
|
G | A | 276 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(273): Show | 278 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.289+331G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109716899 | ||||||
| chr6:109716921
|
G | A | 3 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0004g0006 | 3 | HG02809.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.289+353G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109716921 | ||||||
| chr6:109717008
|
C | CT | 138 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0122others(135): Show | 139 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.289+457dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109717008 | |||||
| chr6:109717008
|
C | CTT | 7 | a0001c0001t0002g0198a0002c0002t0001g0130a0002c0002t0005g0125others(4): Show | 7 | HG01943.hp1 HG02572.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+456_289+457dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109717008 | |||||
| chr6:109717437
|
A | G | 272 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(269): Show | 274 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.289+869A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109717437 | ||||||
| chr6:109717719
|
C | G | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.289+1151C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109717719 | ||||||
| chr6:109717762
|
G | T | 1 | a0002c0004t0001g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.289+1194G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109717762 | ||||||
| chr6:109717951
|
C | T | 153 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(150): Show | 154 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.289+1383C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109717951 | ||||||
| chr6:109717958
|
G | A | 1 | a0002c0014t0002g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.289+1390G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109717958 | ||||||
| chr6:109718216
|
A | G | 2 | a0002c0004t0001g0066a0002c0004t0001g0067 | 2 | NA18961.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.289+1648A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718216 | ||||||
| chr6:109718283
|
C | T | 1 | a0001c0001t0002g0095 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.289+1715C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718283 | ||||||
| chr6:109718537
|
G | T | 60 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0003g0001others(57): Show | 61 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.289+1969G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718537 | ||||||
| chr6:109718639
|
C | T | 56 | a0001c0001t0003g0001a0001c0001t0003g0162a0001c0001t0003g0163others(53): Show | 57 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.289+2071C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718639 | ||||||
| chr6:109718818
|
A | G | 1 | a0002c0002t0004g0204 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.289+2250A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718818 | ||||||
| chr6:109718912
|
C | T | 3 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0004g0238 | 3 | HG02280.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.289+2344C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718912 | ||||||
| chr6:109718920
|
A | AT | 104 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(101): Show | 105 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.289+2368dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109718920 | |||||
| chr6:109718920
|
AT | A | 54 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(51): Show | 54 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.289+2368delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109718920 | |||||
| chr6:109718953
|
G | A | 1 | a0001c0003t0001g0033 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.289+2385G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718953 | ||||||
| chr6:109719323
|
C | T | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+2755C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109719323 | ||||||
| chr6:109719532
|
T | C | 1 | a0002c0002t0004g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.289+2964T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109719532 | ||||||
| chr6:109719535
|
C | T | 2 | a0001c0001t0002g0299a0002c0002t0002g0298 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.289+2967C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109719535 | ||||||
| chr6:109719740
|
T | C | 1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.289+3172T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109719740 | ||||||
| chr6:109719931
|
G | T | 1 | a0002c0004t0001g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.289+3363G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109719931 | ||||||
| chr6:109720344
|
A | T | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.289+3776A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720344 | ||||||
| chr6:109720442
|
T | C | 1 | a0002c0004t0001g0131 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.289+3874T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720442 | ||||||
| chr6:109720448
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.289+3880A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720448 | ||||||
| chr6:109720618
|
A | G | 1 | a0002c0002t0004g0356 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.289+4050A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720618 | ||||||
| chr6:109720638
|
T | A | 1 | a0003c0005t0001g0332 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.289+4070T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720638 | ||||||
| chr6:109720712
|
T | G | 2 | a0002c0002t0004g0359a0002c0002t0004g0360 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.289+4144T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720712 | ||||||
| chr6:109720819
|
C | T | 1 | a0001c0003t0001g0283 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.289+4251C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720819 | ||||||
| chr6:109720820
|
G | A | 1 | a0004c0006t0001g0307 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.289+4252G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720820 | ||||||
| chr6:109721054
|
C | T | 1 | a0001c0003t0001g0280 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.289+4486C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109721054 | ||||||
| chr6:109721096
|
G | A | 9 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0003t0001g0020others(6): Show | 9 | HG00408.hp1 HG00544.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.289+4528G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109721096 | ||||||
| chr6:109721359
|
G | C | 273 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(270): Show | 275 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.289+4791G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109721359 | ||||||
| chr6:109721366
|
C | T | 1 | a0001c0001t0003g0193 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.289+4798C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109721366 | ||||||
| chr6:109721577
|
G | A | 65 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(62): Show | 66 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.289+5009G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109721577 | ||||||
| chr6:109721713
|
A | G | 2 | a0002c0004t0001g0219a0002c0004t0001g0220 | 2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.289+5145A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109721713 | ||||||
| chr6:109722161
|
T | C | 65 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(62): Show | 66 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.290-4948T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109722161 | ||||||
| chr6:109722396
|
C | T | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-4713C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109722396 | ||||||
| chr6:109722480
|
A | G | 1 | a0001c0003t0001g0188 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.290-4629A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109722480 | ||||||
| chr6:109722525
|
G | GAC | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-4572_290-4571d others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109722525 | |||||
| chr6:109722610
|
T | TTA | 4 | a0001c0003t0001g0300a0001c0003t0001g0301a0002c0002t0002g0298others(1): Show | 4 | HG01256.hp1 HG01258.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-4483_290-4482d others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109722610 | |||||
| chr6:109722702
|
A | G | 1 | a0003c0005t0001g0327 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.290-4407A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109722702 | ||||||
| chr6:109722735
|
AG | A | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.290-4371delG | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109722735 | |||||
| chr6:109722996
|
CA | C | 273 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(270): Show | 275 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.290-4111delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109722996 | |||||
| chr6:109723059
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.290-4050C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109723059 | ||||||
| chr6:109723237
|
G | A | 1 | a0002c0004t0001g0037 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.290-3872G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109723237 | ||||||
| chr6:109723808
|
T | C | 1 | a0003c0005t0001g0349 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.290-3301T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109723808 | ||||||
| chr6:109724018
|
G | A | 2 | a0002c0002t0002g0012a0002c0002t0002g0013 | 2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.290-3091G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724018 | ||||||
| chr6:109724073
|
C | T | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.290-3036C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724073 | ||||||
| chr6:109724110
|
C | T | 2 | a0001c0001t0002g0065a0002c0004t0001g0064 | 2 | HG01169.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.290-2999C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724110 | ||||||
| chr6:109724120
|
G | A | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.290-2989G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724120 | ||||||
| chr6:109724140
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.290-2969C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724140 | ||||||
| chr6:109724278
|
C | T | 3 | a0001c0001t0002g0198a0002c0002t0004g0196a0002c0004t0001g0199 | 3 | HG02572.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.290-2831C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724278 | ||||||
| chr6:109724330
|
C | T | 1 | a0003c0007t0001g0347 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.290-2779C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724330 | ||||||
| chr6:109724364
|
T | C | 4 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0002g0008others(1): Show | 4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2745T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724364 | ||||||
| chr6:109724803
|
T | TTG | 7 | a0001c0001t0003g0364a0001c0001t0003g0365a0001c0001t0003g0366others(4): Show | 7 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.290-2278_290-2277d others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109724803 | |||||
| chr6:109724803
|
T | TTGTG | 14 | a0001c0001t0003g0155a0001c0001t0003g0156a0002c0002t0002g0009others(11): Show | 14 | HG02280.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.290-2280_290-2277d others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109724803 | |||||
| chr6:109724803
|
T | TTGTGTG | 4 | a0002c0002t0002g0086a0002c0002t0005g0125a0002c0002t0005g0126others(1): Show | 4 | HG02486.hp2 HG03453.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2282_290-2277d others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109724803 | |||||
| chr6:109724803
|
TTG | T | 51 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(48): Show | 51 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.290-2278_290-2277d others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109724803 | |||||
| chr6:109724830
|
T | TAC | 8 | a0001c0003t0001g0285a0001c0003t0001g0296a0001c0003t0001g0297others(5): Show | 8 | HG01346.hp2 HG01361.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.290-2279_290-2278i others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724830 | ||||||
| chr6:109724831
|
G | A | 114 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(111): Show | 114 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.290-2278G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724831 | ||||||
| chr6:109724832
|
T | C | 105 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(102): Show | 105 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.290-2277T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724832 | ||||||
| chr6:109724834
|
C | CAT | 12 | a0001c0003t0001g0014a0001c0003t0001g0165a0001c0003t0001g0166others(9): Show | 13 | HG00741.hp1 HG01433.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.290-2260_290-2259d others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109724834 | |||||
| chr6:109724834
|
C | T | 114 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(111): Show | 114 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.290-2275C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724834 | ||||||
| chr6:109724944
|
T | G | 43 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(40): Show | 43 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.290-2165T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724944 | ||||||
| chr6:109724996
|
A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-2113A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724996 | ||||||
| chr6:109725052
|
G | A | 2 | a0002c0004t0001g0215a0002c0004t0001g0216 | 2 | HG01346.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.290-2057G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725052 | ||||||
| chr6:109725071
|
GAATTA | G | 3 | a0001c0001t0002g0351a0001c0001t0002g0353a0002c0002t0004g0352 | 3 | HG03239.hp2 HG03654.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.290-2033_290-2029d others(7): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109725071 | |||||
| chr6:109725101
|
A | T | 4 | a0001c0001t0002g0267a0001c0001t0002g0268a0002c0002t0001g0148others(1): Show | 4 | HG01071.hp1 HG01123.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2008A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725101 | ||||||
| chr6:109725182
|
A | G | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.290-1927A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725182 | ||||||
| chr6:109725197
|
A | G | 2 | a0002c0002t0002g0084a0002c0002t0002g0085 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.290-1912A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725197 | ||||||
| chr6:109725278
|
G | C | 1 | a0002c0002t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.290-1831G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725278 | ||||||
| chr6:109725279
|
G | A | 1 | a0002c0002t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.290-1830G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725279 | ||||||
| chr6:109725419
|
C | A | 108 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(105): Show | 109 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.290-1690C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725419 | ||||||
| chr6:109725487
|
T | A | 3 | a0003c0005t0001g0329a0003c0005t0001g0330a0003c0005t0001g0331 | 3 | HG02074.hp2 NA18952.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.290-1622T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725487 | ||||||
| chr6:109725681
|
C | T | 3 | a0001c0001t0002g0015a0001c0001t0002g0017a0005c0019t0006g0016 | 3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.290-1428C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725681 | ||||||
| chr6:109725692
|
A | C | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | HG00423.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.290-1417A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725692 | ||||||
| chr6:109725737
|
T | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-1372T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725737 | ||||||
| chr6:109725919
|
A | G | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-1190A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725919 | ||||||
| chr6:109725998
|
A | C | 2 | a0002c0002t0004g0359a0002c0002t0004g0360 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.290-1111A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725998 | ||||||
| chr6:109726021
|
T | G | 1 | a0002c0004t0001g0131 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.290-1088T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726021 | ||||||
| chr6:109726037
|
C | T | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-1072C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726037 | ||||||
| chr6:109726061
|
G | C | 280 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0122others(277): Show | 282 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(279): Show |
intron_variant | MODIFIER | c.290-1048G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726061 | ||||||
| chr6:109726125
|
TG | T | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.290-982delG | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109726125 | |||||
| chr6:109726127
|
G | C | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.290-982G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726127 | ||||||
| chr6:109726524
|
C | A | 1 | a0002c0002t0002g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.290-585C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726524 | ||||||
| chr6:109726563
|
G | A | 1 | a0001c0003t0001g0252 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.290-546G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726563 | ||||||
| chr6:109726625
|
T | C | 43 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(40): Show | 43 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.290-484T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726625 | ||||||
| chr6:109726642
|
A | G | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.290-467A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726642 | ||||||
| chr6:109726847
|
G | A | 3 | a0003c0005t0001g0329a0003c0005t0001g0330a0003c0005t0001g0331 | 3 | HG02074.hp2 NA18952.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.290-262G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726847 | ||||||
| chr6:109726962
|
C | T | 273 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(270): Show | 275 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.290-147C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726962 | ||||||
| chr6:109727059
|
G | A | 1 | a0002c0004t0001g0216 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.290-50G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109727059 | ||||||
| chr6:109727286
|
C | CT | 272 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(269): Show | 274 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.446+32dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 109727286 | |||||
| chr6:109727648
|
A | C | 1 | a0001c0001t0003g0169 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.446+383A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109727648 | ||||||
| chr6:109727930
|
C | T | 1 | a0001c0003t0001g0033 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.446+665C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109727930 | ||||||
| chr6:109727977
|
G | A | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.446+712G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109727977 | ||||||
| chr6:109728011
|
A | T | 1 | a0002c0004t0001g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.446+746A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728011 | ||||||
| chr6:109728108
|
C | T | 1 | a0005c0019t0006g0016 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.446+843C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728108 | ||||||
| chr6:109728221
|
T | C | 1 | a0001c0003t0001g0097 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.446+956T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728221 | ||||||
| chr6:109728306
|
T | C | 43 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(40): Show | 43 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.446+1041T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728306 | ||||||
| chr6:109728492
|
G | A | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.446+1227G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728492 | ||||||
| chr6:109728620
|
G | A | 43 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(40): Show | 43 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.446+1355G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728620 | ||||||
| chr6:109728839
|
G | A | 273 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(270): Show | 275 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.446+1574G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728839 | ||||||
| chr6:109728864
|
A | T | 1 | a0002c0002t0002g0363 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.446+1599A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728864 | ||||||
| chr6:109728901
|
T | A | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.446+1636T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728901 | ||||||
| chr6:109729051
|
T | C | 7 | a0001c0001t0002g0351a0001c0001t0002g0353a0002c0002t0004g0352others(4): Show | 7 | HG01081.hp1 HG02965.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.446+1786T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729051 | ||||||
| chr6:109729387
|
T | C | 1 | a0001c0003t0001g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.446+2122T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729387 | ||||||
| chr6:109729765
|
C | A | 1 | a0001c0001t0002g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.446+2500C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729765 | ||||||
| chr6:109729773
|
CA | C | 198 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(195): Show | 200 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.446+2524delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 109729773 | |||||
| chr6:109729777
|
A | C | 2 | a0002c0002t0002g0362a0002c0002t0002g0363 | 2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.446+2512A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729777 | ||||||
| chr6:109729792
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.446+2527T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729792 | ||||||
| chr6:109729821
|
T | C | 1 | a0002c0002t0002g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.446+2556T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729821 | ||||||
| chr6:109729938
|
T | G | 213 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(210): Show | 215 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.446+2673T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729938 | ||||||
| chr6:109730137
|
C | T | 2 | a0002c0002t0002g0012a0002c0002t0002g0013 | 2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.447-2500C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730137 | ||||||
| chr6:109730190
|
A | G | 3 | a0001c0001t0002g0198a0002c0002t0004g0196a0002c0004t0001g0199 | 3 | HG02572.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.447-2447A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730190 | ||||||
| chr6:109730309
|
A | G | 1 | a0001c0003t0001g0319 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.447-2328A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730309 | ||||||
| chr6:109730679
|
G | T | 34 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(31): Show | 34 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.447-1958G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730679 | ||||||
| chr6:109730756
|
A | C | 1 | a0002c0002t0002g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.447-1881A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730756 | ||||||
| chr6:109730801
|
G | A | 2 | a0001c0003t0001g0034a0001c0003t0001g0035 | 2 | NA19002.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.447-1836G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730801 | ||||||
| chr6:109730827
|
G | A | 43 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(40): Show | 43 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.447-1810G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730827 | ||||||
| chr6:109730886
|
T | TTTGCCTT others(16): Show |
2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.447-1748_447-1747i others(25): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 109730886 | |||||
| chr6:109730893
|
C | T | 12 | a0001c0001t0003g0001a0001c0001t0003g0162a0001c0001t0003g0168others(9): Show | 13 | NA18939.hp1 NA18940.hp1 NA18956.hp2 others(10): Show |
intron_variant | MODIFIER | c.447-1744C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730893 | ||||||
| chr6:109730907
|
A | G | 3 | a0002c0002t0001g0130a0002c0002t0001g0146a0002c0002t0001g0147 | 3 | HG01943.hp1 HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.447-1730A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730907 | ||||||
| chr6:109731067
|
G | C | 48 | a0003c0005t0001g0002a0003c0005t0001g0068a0003c0005t0001g0249others(45): Show | 49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.447-1570G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731067 | ||||||
| chr6:109731312
|
A | G | 62 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(59): Show | 63 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(60): Show |
intron_variant | MODIFIER | c.447-1325A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731312 | ||||||
| chr6:109731323
|
G | A | 1 | a0002c0002t0004g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.447-1314G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731323 | ||||||
| chr6:109731652
|
A | G | 1 | a0003c0005t0001g0346 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.447-985A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731652 | ||||||
| chr6:109731677
|
G | T | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.447-960G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731677 | ||||||
| chr6:109731775
|
G | A | 1 | a0002c0002t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.447-862G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731775 | ||||||
| chr6:109731870
|
A | G | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.447-767A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731870 | ||||||
| chr6:109732047
|
T | A | 53 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(50): Show | 53 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.447-590T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732047 | ||||||
| chr6:109732073
|
T | C | 151 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(148): Show | 152 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.447-564T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732073 | ||||||
| chr6:109732253
|
G | T | 48 | a0003c0005t0001g0002a0003c0005t0001g0068a0003c0005t0001g0249others(45): Show | 49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.447-384G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732253 | ||||||
| chr6:109732440
|
A | G | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.447-197A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732440 | ||||||
| chr6:109732467
|
A | G | 1 | a0002c0002t0004g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.447-170A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732467 | ||||||
| chr6:109732518
|
T | G | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.447-119T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732518 | ||||||
| chr6:109732544
|
T | C | 10 | a0001c0003t0001g0014a0001c0003t0001g0165a0001c0003t0001g0166others(7): Show | 10 | HG00741.hp1 HG01433.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.447-93T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732544 | ||||||
| chr6:109732621
|
G | GT | 277 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0122others(274): Show | 279 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
splice_acceptor_variant&intron_variant | HIGH | c.447-3dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 109732621 | |||||
| chr6:109732748
|
G | A | 3 | a0001c0001t0003g0155a0001c0001t0003g0156a0002c0002t0002g0210 | 3 | HG02896.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.497+61G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109732748 | ||||||
| chr6:109732862
|
A | T | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.497+175A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109732862 | ||||||
| chr6:109732911
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.497+224C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109732911 | ||||||
| chr6:109732914
|
T | A | 34 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(31): Show | 34 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.497+227T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109732914 | ||||||
| chr6:109732933
|
T | C | 34 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(31): Show | 34 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.497+246T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109732933 | ||||||
| chr6:109733283
|
G | A | 151 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(148): Show | 152 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.497+596G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109733283 | ||||||
| chr6:109733321
|
T | C | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497+634T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109733321 | ||||||
| chr6:109733356
|
G | A | 1 | a0003c0005t0001g0068 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.497+669G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109733356 | ||||||
| chr6:109733640
|
A | G | 9 | a0001c0001t0002g0198a0002c0002t0004g0196a0002c0002t0004g0197others(6): Show | 9 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.497+953A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109733640 | ||||||
| chr6:109733828
|
CCTT | C | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.497+1149_497+1151d others(5): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr6 | 109733828 | |||||
| chr6:109733949
|
G | T | 1 | a0003c0005t0001g0326 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.498-1201G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109733949 | ||||||
| chr6:109734060
|
A | T | 1 | a0002c0002t0002g0083 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.498-1090A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734060 | ||||||
| chr6:109734110
|
G | A | 62 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(59): Show | 63 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(60): Show |
intron_variant | MODIFIER | c.498-1040G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734110 | ||||||
| chr6:109734500
|
AC | A | 6 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(3): Show | 6 | HG00099.hp2 HG00639.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-649delC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734500 | ||||||
| chr6:109734666
|
T | C | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.498-484T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734666 | ||||||
| chr6:109734782
|
G | A | 273 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(270): Show | 275 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.498-368G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734782 | ||||||
| chr6:109734860
|
T | G | 1 | a0001c0001t0003g0190 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.498-290T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734860 | ||||||
| chr6:109734867
|
T | C | 1 | a0001c0001t0002g0038 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.498-283T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734867 | ||||||
| chr6:109735012
|
A | G | 2 | a0002c0004t0001g0215a0002c0004t0001g0216 | 2 | HG01346.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.498-138A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109735012 | ||||||
| chr6:109735048
|
G | A | 1 | a0001c0003t0001g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.498-102G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109735048 | ||||||
| chr6:109735063
|
T | C | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.498-87T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109735063 | ||||||
| chr6:109735653
|
A | T | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.646+355A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109735653 | ||||||
| chr6:109735800
|
G | C | 1 | a0002c0002t0002g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.646+502G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109735800 | ||||||
| chr6:109736016
|
A | G | 273 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(270): Show | 275 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.646+718A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109736016 | ||||||
| chr6:109736025
|
G | A | 2 | a0001c0001t0002g0299a0002c0002t0002g0298 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.646+727G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109736025 | ||||||
| chr6:109736204
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0002g0017 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.646+906G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109736204 | ||||||
| chr6:109736727
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.646+1429T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109736727 | ||||||
| chr6:109736860
|
G | T | 1 | a0001c0003t0001g0097 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.647-1465G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109736860 | ||||||
| chr6:109737108
|
G | A | 43 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(40): Show | 43 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.647-1217G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737108 | ||||||
| chr6:109737153
|
C | T | 1 | a0002c0004t0001g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.647-1172C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737153 | ||||||
| chr6:109737237
|
T | G | 1 | a0001c0003t0001g0034 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.647-1088T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737237 | ||||||
| chr6:109737486
|
G | A | 1 | a0001c0003t0001g0293 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.647-839G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737486 | ||||||
| chr6:109737680
|
G | A | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.647-645G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737680 | ||||||
| chr6:109737749
|
C | T | 29 | a0001c0003t0001g0145a0002c0002t0001g0130a0002c0002t0001g0132others(26): Show | 29 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.647-576C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737749 | ||||||
| chr6:109737793
|
A | G | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.647-532A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737793 | ||||||
| chr6:109737797
|
G | A | 53 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(50): Show | 53 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.647-528G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737797 | ||||||
| chr6:109737837
|
C | T | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.647-488C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737837 | ||||||
| chr6:109737974
|
C | T | 1 | a0001c0001t0002g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.647-351C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737974 | ||||||
| chr6:109737986
|
G | A | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.647-339G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737986 | ||||||
| chr6:109738236
|
T | C | 1 | a0001c0003t0001g0073 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.647-89T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109738236 | ||||||
| chr6:109738277
|
C | T | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.647-48C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109738277 | ||||||
| chr6:109738307
|
C | A | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.647-18C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109738307 | ||||||
| chr6:109738751
|
G | A | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.775+298G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109738751 | ||||||
| chr6:109738766
|
A | G | 6 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(3): Show | 6 | HG00558.hp2 NA18952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+313A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109738766 | ||||||
| chr6:109738815
|
G | A | 12 | a0002c0002t0002g0110a0002c0002t0002g0111a0002c0002t0002g0112others(9): Show | 12 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.775+362G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109738815 | ||||||
| chr6:109738833
|
C | CAG | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.775+392_775+393dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 109738833 | |||||
| chr6:109739246
|
AC | A | 151 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(148): Show | 152 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.775+794delC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739246 | ||||||
| chr6:109739407
|
C | T | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.775+954C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739407 | ||||||
| chr6:109739433
|
G | A | 6 | a0002c0004t0001g0028a0002c0004t0001g0039a0002c0004t0001g0040others(3): Show | 6 | HG02056.hp1 HG02071.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+980G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739433 | ||||||
| chr6:109739488
|
G | A | 1 | a0002c0002t0002g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.775+1035G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739488 | ||||||
| chr6:109739615
|
C | T | 120 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(117): Show | 121 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(118): Show |
intron_variant | MODIFIER | c.775+1162C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739615 | ||||||
| chr6:109739666
|
C | T | 23 | a0001c0001t0002g0226a0001c0003t0001g0014a0001c0003t0001g0165others(20): Show | 23 | HG01433.hp1 HG01934.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.775+1213C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739666 | ||||||
| chr6:109739706
|
T | C | 1 | a0001c0001t0002g0042 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.775+1253T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739706 | ||||||
| chr6:109739877
|
C | T | 48 | a0003c0005t0001g0002a0003c0005t0001g0068a0003c0005t0001g0249others(45): Show | 49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.775+1424C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739877 | ||||||
| chr6:109740253
|
A | T | 1 | a0001c0003t0001g0278 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.776-1191A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740253 | ||||||
| chr6:109740350
|
C | T | 11 | a0001c0001t0002g0198a0002c0002t0004g0196a0002c0002t0004g0197others(8): Show | 11 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.776-1094C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740350 | ||||||
| chr6:109740413
|
A | G | 2 | a0002c0002t0002g0009a0002c0002t0002g0010 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.776-1031A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740413 | ||||||
| chr6:109740652
|
G | C | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.776-792G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740652 | ||||||
| chr6:109740708
|
C | T | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.776-736C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740708 | ||||||
| chr6:109740878
|
A | G | 12 | a0002c0002t0002g0110a0002c0002t0002g0111a0002c0002t0002g0112others(9): Show | 12 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.776-566A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740878 | ||||||
| chr6:109740895
|
A | T | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.776-549A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740895 | ||||||
| chr6:109741020
|
C | A | 273 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(270): Show | 275 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.776-424C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109741020 | ||||||
| chr6:109741085
|
G | C | 46 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(43): Show | 46 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.776-359G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109741085 | ||||||
| chr6:109741135
|
G | C | 2 | a0001c0003t0001g0281a0001c0003t0001g0282 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.776-309G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109741135 | ||||||
| chr6:109741149
|
C | T | 1 | a0002c0004t0001g0256 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.776-295C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109741149 | ||||||
| chr6:109741174
|
C | T | 6 | a0001c0001t0002g0221a0001c0001t0002g0223a0001c0001t0002g0224others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.776-270C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109741174 | ||||||
| chr6:109741348
|
G | T | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.776-96G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109741348 | ||||||
| chr6:109741670
|
T | G | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.876+126T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | chr6 | 109741670 | ||||||
| chr6:109741784
|
C | T | 2 | a0002c0002t0002g0084a0002c0002t0002g0085 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.876+240C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | chr6 | 109741784 | ||||||
| chr6:109741825
|
A | G | 15 | a0002c0002t0001g0130a0002c0002t0001g0138a0002c0002t0001g0141others(12): Show | 15 | HG01943.hp1 HG01975.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.876+281A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | chr6 | 109741825 | ||||||
| chr6:109741908
|
G | A | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+364G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | chr6 | 109741908 | ||||||
| chr6:109742426
|
T | C | 18 | a0003c0005t0001g0332a0003c0005t0001g0333a0003c0005t0001g0334others(15): Show | 18 | HG02155.hp2 NA18940.hp2 NA18947.hp1 others(15): Show |
intron_variant | MODIFIER | c.877-684T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | chr6 | 109742426 | ||||||
| chr6:109742495
|
G | T | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.877-615G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | chr6 | 109742495 | ||||||
| chr6:109743052
|
TATTTC | T | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.877-54_877-50delTC others(3): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr6 | 109743052 | |||||
| chr6:109743378
|
G | A | 1 | a0001c0003t0001g0021 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1039+106G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 9/22 | chr6 | 109743378 | ||||||
| chr6:109743577
|
T | G | 67 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(64): Show | 68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1040-98T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 9/22 | chr6 | 109743577 | ||||||
| chr6:109743846
|
TAAC | T | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1137+77_1137+79del others(3): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109743846 | |||||
| chr6:109743883
|
G | A | 67 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(64): Show | 68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1137+111G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109743883 | ||||||
| chr6:109743984
|
G | A | 1 | a0001c0003t0001g0264 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1137+212G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109743984 | ||||||
| chr6:109744165
|
A | G | 1 | a0002c0002t0003g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1137+393A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744165 | ||||||
| chr6:109744227
|
G | T | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1137+455G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744227 | ||||||
| chr6:109744443
|
C | A | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1137+671C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744443 | ||||||
| chr6:109744518
|
C | G | 151 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(148): Show | 152 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1137+746C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744518 | ||||||
| chr6:109744811
|
C | T | 1 | a0003c0005t0001g0345 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1137+1039C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744811 | ||||||
| chr6:109744830
|
C | T | 1 | a0001c0003t0001g0266 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1137+1058C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744830 | ||||||
| chr6:109744835
|
T | C | 155 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(152): Show | 156 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1137+1063T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744835 | ||||||
| chr6:109744907
|
C | G | 40 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(37): Show | 40 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1137+1135C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744907 | ||||||
| chr6:109744984
|
C | T | 1 | a0002c0002t0004g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1137+1212C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744984 | ||||||
| chr6:109744995
|
T | C | 19 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0090others(16): Show | 19 | HG00423.hp1 NA18747.hp1 NA18953.hp1 others(16): Show |
intron_variant | MODIFIER | c.1137+1223T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744995 | ||||||
| chr6:109745001
|
A | G | 1 | a0002c0002t0002g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1137+1229A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109745001 | ||||||
| chr6:109745249
|
C | T | 3 | a0001c0001t0003g0364a0001c0001t0003g0365a0001c0001t0003g0366 | 3 | HG02615.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1137+1477C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109745249 | ||||||
| chr6:109745369
|
G | A | 1 | a0004c0008t0002g0323 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1137+1597G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109745369 | ||||||
| chr6:109745732
|
G | A | 57 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(54): Show | 57 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1137+1960G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109745732 | ||||||
| chr6:109745901
|
C | T | 3 | a0001c0001t0002g0015a0001c0001t0002g0017a0005c0019t0006g0016 | 3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1137+2129C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109745901 | ||||||
| chr6:109746003
|
A | G | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1137+2231A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746003 | ||||||
| chr6:109746078
|
A | G | 1 | a0002c0002t0004g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1137+2306A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746078 | ||||||
| chr6:109746202
|
C | T | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1137+2430C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746202 | ||||||
| chr6:109746216
|
C | T | 4 | a0001c0003t0001g0296a0001c0003t0001g0297a0001c0003t0001g0302others(1): Show | 4 | HG01346.hp2 HG01361.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137+2444C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746216 | ||||||
| chr6:109746279
|
C | G | 3 | a0001c0001t0002g0015a0001c0001t0002g0017a0005c0019t0006g0016 | 3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1137+2507C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746279 | ||||||
| chr6:109746301
|
C | T | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1137+2529C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746301 | ||||||
| chr6:109746419
|
A | T | 3 | a0001c0001t0002g0015a0001c0001t0002g0017a0005c0019t0006g0016 | 3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1137+2647A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746419 | ||||||
| chr6:109746489
|
A | G | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1137+2717A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746489 | ||||||
| chr6:109746569
|
G | A | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137+2797G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746569 | ||||||
| chr6:109746570
|
G | A | 62 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(59): Show | 63 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(60): Show |
intron_variant | MODIFIER | c.1137+2798G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746570 | ||||||
| chr6:109746697
|
C | G | 11 | a0001c0003t0001g0014a0001c0003t0001g0097a0001c0003t0001g0165others(8): Show | 11 | HG00741.hp1 HG01433.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.1137+2925C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746697 | ||||||
| chr6:109746881
|
A | T | 1 | a0002c0002t0004g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1137+3109A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746881 | ||||||
| chr6:109746887
|
G | A | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137+3115G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746887 | ||||||
| chr6:109746958
|
C | T | 1 | a0002c0002t0002g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1137+3186C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746958 | ||||||
| chr6:109747089
|
G | A | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1137+3317G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109747089 | ||||||
| chr6:109747119
|
C | T | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1137+3347C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109747119 | ||||||
| chr6:109747147
|
G | A | 4 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127others(1): Show | 4 | HG03453.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137+3375G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109747147 | ||||||
| chr6:109747411
|
G | A | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1137+3639G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109747411 | ||||||
| chr6:109747516
|
A | G | 2 | a0002c0004t0001g0066a0002c0004t0001g0067 | 2 | NA18961.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1137+3744A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109747516 | ||||||
| chr6:109747583
|
A | T | 155 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(152): Show | 156 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1137+3811A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109747583 | ||||||
| chr6:109748147
|
T | C | 48 | a0003c0005t0001g0002a0003c0005t0001g0068a0003c0005t0001g0249others(45): Show | 49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.1137+4375T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748147 | ||||||
| chr6:109748250
|
T | C | 1 | a0003c0005t0001g0312 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1137+4478T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748250 | ||||||
| chr6:109748267
|
G | A | 273 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(270): Show | 275 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.1137+4495G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748267 | ||||||
| chr6:109748325
|
G | T | 1 | a0001c0003t0001g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1137+4553G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748325 | ||||||
| chr6:109748354
|
G | A | 1 | a0004c0006t0001g0307 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1137+4582G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748354 | ||||||
| chr6:109748464
|
A | C | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137+4692A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748464 | ||||||
| chr6:109748501
|
A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1137+4729A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748501 | ||||||
| chr6:109748756
|
G | A | 1 | a0001c0003t0001g0031 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1137+4984G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748756 | ||||||
| chr6:109748819
|
G | A | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1137+5047G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748819 | ||||||
| chr6:109748875
|
A | G | 1 | a0002c0002t0004g0356 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1137+5103A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748875 | ||||||
| chr6:109748919
|
C | T | 2 | a0002c0004t0001g0061a0002c0004t0001g0062 | 2 | HG00423.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1137+5147C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748919 | ||||||
| chr6:109748932
|
G | A | 15 | a0001c0001t0002g0198a0002c0002t0002g0164a0002c0002t0004g0196others(12): Show | 15 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1137+5160G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748932 | ||||||
| chr6:109749026
|
A | G | 4 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0002g0008others(1): Show | 4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137+5254A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749026 | ||||||
| chr6:109749055
|
C | CTG | 33 | a0001c0001t0002g0029a0001c0001t0002g0050a0001c0001t0002g0080others(30): Show | 33 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1137+5331_1137+533 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
C | CTGTG | 40 | a0001c0001t0002g0018a0001c0001t0002g0025a0001c0001t0002g0032others(37): Show | 40 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1137+5329_1137+533 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
C | CTGTGTG | 25 | a0001c0001t0002g0019a0001c0001t0002g0042a0001c0001t0002g0090others(22): Show | 25 | HG00323.hp2 HG00438.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1137+5327_1137+533 others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
C | CTGTGTGT others(1): Show |
8 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0304others(5): Show | 8 | HG01361.hp1 HG01517.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1137+5325_1137+533 others(12): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
C | CTGTGTGT others(3): Show |
15 | a0001c0003t0001g0034a0001c0003t0001g0292a0001c0003t0001g0293others(12): Show | 15 | HG00544.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1137+5323_1137+533 others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
C | CTGTGTGT others(5): Show |
10 | a0001c0003t0001g0291a0001c0003t0001g0302a0002c0002t0001g0130others(7): Show | 10 | HG01346.hp2 HG01943.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137+5321_1137+533 others(16): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
C | CTGTGTGT others(7): Show |
7 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0146others(4): Show | 7 | HG01975.hp1 HG02015.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1137+5319_1137+533 others(18): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
C | CTGTGTGT others(9): Show |
3 | a0001c0003t0001g0297a0002c0002t0001g0138a0002c0002t0001g0149 | 3 | HG02135.hp2 NA18951.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1137+5317_1137+533 others(20): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
CTG | C | 73 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(70): Show | 74 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1137+5331_1137+533 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
CTGTG | C | 5 | a0002c0002t0002g0362a0002c0002t0005g0125a0002c0004t0001g0063others(2): Show | 6 | HG02895.hp2 NA18982.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137+5329_1137+533 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
CTGTGTG | C | 16 | a0001c0001t0002g0213a0001c0001t0002g0217a0001c0001t0002g0227others(13): Show | 16 | HG00735.hp1 HG01069.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1137+5327_1137+533 others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
CTGTGTGT others(1): Show |
C | 38 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0198others(35): Show | 38 | HG00099.hp2 HG00639.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.1137+5325_1137+533 others(12): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
CTGTGTGT others(7): Show |
C | 1 | a0003c0005t0001g0333 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1137+5319_1137+533 others(18): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749055
|
CTGTGTGT others(21): Show |
C | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1137+5305_1137+533 others(32): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | |||||
| chr6:109749104
|
T | TGTGTGTG others(4): Show |
1 | a0002c0004t0001g0128 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1137+5332_1137+533 others(15): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749104 | ||||||
| chr6:109749178
|
C | T | 1 | a0001c0003t0001g0031 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1137+5406C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749178 | ||||||
| chr6:109749425
|
T | G | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137+5653T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749425 | ||||||
| chr6:109749564
|
A | G | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1137+5792A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749564 | ||||||
| chr6:109749588
|
T | TAATAAAA others(3): Show |
11 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(8): Show | 11 | HG02258.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1137+5839_1137+584 others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749588 | |||||
| chr6:109749588
|
T | TAATAAAA others(8): Show |
106 | a0001c0001t0002g0198a0001c0001t0002g0214a0001c0001t0002g0217others(103): Show | 107 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.1137+5834_1137+584 others(19): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749588 | |||||
| chr6:109749588
|
T | TAATAAAA others(13): Show |
114 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0213others(111): Show | 115 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.1137+5829_1137+584 others(24): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749588 | |||||
| chr6:109749588
|
T | TAATAAAA others(18): Show |
32 | a0001c0001t0002g0289a0001c0001t0002g0304a0001c0003t0001g0014others(29): Show | 32 | HG00408.hp2 HG00741.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1137+5824_1137+584 others(29): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749588 | |||||
| chr6:109749588
|
T | TAATAAAA others(23): Show |
7 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0262others(4): Show | 7 | HG00738.hp2 HG01099.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1137+5819_1137+584 others(34): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749588 | |||||
| chr6:109749723
|
C | T | 1 | a0004c0008t0002g0323 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1137+5951C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749723 | ||||||
| chr6:109749753
|
A | G | 1 | a0003c0005t0001g0350 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1137+5981A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749753 | ||||||
| chr6:109749766
|
T | G | 109 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(106): Show | 110 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1137+5994T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749766 | ||||||
| chr6:109749783
|
G | A | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1137+6011G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749783 | ||||||
| chr6:109750116
|
C | A | 109 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(106): Show | 110 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1137+6344C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750116 | ||||||
| chr6:109750159
|
C | T | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137+6387C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750159 | ||||||
| chr6:109750166
|
C | A | 1 | a0001c0001t0002g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1137+6394C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750166 | ||||||
| chr6:109750231
|
A | G | 1 | a0003c0005t0001g0320 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1137+6459A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750231 | ||||||
| chr6:109750327
|
A | T | 1 | a0002c0004t0001g0067 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1137+6555A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750327 | ||||||
| chr6:109750394
|
G | A | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1137+6622G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750394 | ||||||
| chr6:109750426
|
G | T | 2 | a0001c0010t0002g0026a0001c0010t0002g0027 | 2 | HG01258.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1137+6654G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750426 | ||||||
| chr6:109750448
|
G | A | 6 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(3): Show | 6 | HG00558.hp2 NA18952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1137+6676G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750448 | ||||||
| chr6:109750509
|
C | T | 1 | a0002c0002t0004g0360 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1137+6737C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750509 | ||||||
| chr6:109750611
|
C | T | 3 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0002g0237 | 3 | HG01099.hp2 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1137+6839C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750611 | ||||||
| chr6:109750717
|
A | G | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137+6945A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750717 | ||||||
| chr6:109750748
|
A | C | 280 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0122others(277): Show | 282 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(279): Show |
intron_variant | MODIFIER | c.1137+6976A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750748 | ||||||
| chr6:109750909
|
A | C | 1 | a0004c0008t0002g0310 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1137+7137A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750909 | ||||||
| chr6:109751001
|
C | T | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1137+7229C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751001 | ||||||
| chr6:109751060
|
A | G | 3 | a0002c0002t0002g0139a0002c0002t0002g0150a0002c0004t0001g0140 | 3 | NA19007.hp2 NA19063.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1137+7288A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751060 | ||||||
| chr6:109751299
|
T | G | 3 | a0001c0001t0003g0364a0001c0001t0003g0365a0001c0001t0003g0366 | 3 | HG02615.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1137+7527T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751299 | ||||||
| chr6:109751300
|
G | A | 67 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(64): Show | 68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1137+7528G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751300 | ||||||
| chr6:109751338
|
G | A | 3 | a0002c0004t0001g0215a0002c0004t0001g0216a0002c0004t0001g0242 | 3 | HG01346.hp1 HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1137+7566G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751338 | ||||||
| chr6:109751398
|
G | A | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1137+7626G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751398 | ||||||
| chr6:109751529
|
G | A | 57 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(54): Show | 57 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1137+7757G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751529 | ||||||
| chr6:109751565
|
C | T | 1 | a0002c0002t0004g0356 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1137+7793C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751565 | ||||||
| chr6:109751706
|
G | A | 1 | a0001c0003t0001g0165 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1137+7934G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751706 | ||||||
| chr6:109751803
|
CT | C | 277 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(274): Show | 279 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.1137+8038delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109751803 | |||||
| chr6:109751960
|
G | A | 2 | a0001c0003t0001g0260a0001c0003t0001g0261 | 2 | HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1137+8188G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751960 | ||||||
| chr6:109751994
|
C | G | 1 | a0002c0002t0004g0356 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1137+8222C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751994 | ||||||
| chr6:109752015
|
A | T | 1 | a0001c0003t0001g0275 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1138-8235A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752015 | ||||||
| chr6:109752084
|
C | T | 1 | a0004c0008t0002g0310 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1138-8166C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752084 | ||||||
| chr6:109752086
|
G | T | 1 | a0002c0004t0001g0041 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1138-8164G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752086 | ||||||
| chr6:109752116
|
A | G | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1138-8134A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752116 | ||||||
| chr6:109752246
|
C | T | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138-8004C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752246 | ||||||
| chr6:109752301
|
G | A | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1138-7949G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752301 | ||||||
| chr6:109752317
|
A | G | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-7933A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752317 | ||||||
| chr6:109752332
|
G | A | 155 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(152): Show | 156 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1138-7918G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752332 | ||||||
| chr6:109752335
|
G | A | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138-7915G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752335 | ||||||
| chr6:109752495
|
T | C | 277 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(274): Show | 279 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.1138-7755T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752495 | ||||||
| chr6:109752525
|
G | A | 52 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0002g0008others(49): Show | 53 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(50): Show |
intron_variant | MODIFIER | c.1138-7725G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752525 | ||||||
| chr6:109752548
|
G | A | 1 | a0002c0002t0004g0207 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1138-7702G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752548 | ||||||
| chr6:109752572
|
C | T | 1 | a0004c0008t0002g0310 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1138-7678C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752572 | ||||||
| chr6:109752573
|
G | A | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1138-7677G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752573 | ||||||
| chr6:109752627
|
T | G | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1138-7623T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752627 | ||||||
| chr6:109752634
|
C | T | 13 | a0001c0001t0002g0289a0001c0003t0001g0257a0001c0003t0001g0258others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1138-7616C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752634 | ||||||
| chr6:109752666
|
T | G | 277 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(274): Show | 279 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.1138-7584T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752666 | ||||||
| chr6:109752736
|
T | A | 3 | a0001c0001t0002g0015a0001c0001t0002g0017a0005c0019t0006g0016 | 3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1138-7514T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752736 | ||||||
| chr6:109752896
|
A | G | 2 | a0002c0002t0002g0009a0002c0002t0002g0010 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1138-7354A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752896 | ||||||
| chr6:109752993
|
T | C | 12 | a0002c0002t0002g0110a0002c0002t0002g0111a0002c0002t0002g0112others(9): Show | 12 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.1138-7257T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752993 | ||||||
| chr6:109753013
|
G | C | 1 | a0001c0001t0002g0091 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1138-7237G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753013 | ||||||
| chr6:109753091
|
A | G | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1138-7159A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753091 | ||||||
| chr6:109753174
|
C | G | 1 | a0001c0001t0002g0091 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1138-7076C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753174 | ||||||
| chr6:109753190
|
C | T | 46 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(43): Show | 46 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1138-7060C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753190 | ||||||
| chr6:109753193
|
G | A | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1138-7057G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753193 | ||||||
| chr6:109753209
|
C | T | 67 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(64): Show | 68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1138-7041C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753209 | ||||||
| chr6:109753255
|
C | T | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | HG00423.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1138-6995C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753255 | ||||||
| chr6:109753262
|
G | T | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-6988G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753262 | ||||||
| chr6:109753313
|
G | C | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-6937G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753313 | ||||||
| chr6:109753323
|
C | A | 1 | a0001c0003t0001g0262 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1138-6927C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753323 | ||||||
| chr6:109753351
|
T | G | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-6899T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753351 | ||||||
| chr6:109753411
|
G | A | 3 | a0003c0005t0001g0249a0003c0005t0001g0350a0003c0017t0001g0314 | 3 | NA18943.hp1 NA18959.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1138-6839G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753411 | ||||||
| chr6:109753411
|
G | C | 2 | a0002c0002t0002g0009a0002c0002t0002g0010 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1138-6839G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753411 | ||||||
| chr6:109753418
|
T | C | 280 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0122others(277): Show | 282 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(279): Show |
intron_variant | MODIFIER | c.1138-6832T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753418 | ||||||
| chr6:109753442
|
A | G | 2 | a0001c0001t0002g0226a0002c0002t0002g0225 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1138-6808A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753442 | ||||||
| chr6:109753801
|
CTT | C | 3 | a0002c0002t0004g0355a0002c0002t0004g0356a0002c0002t0004g0357 | 3 | HG01081.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1138-6447_1138-644 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109753801 | |||||
| chr6:109753864
|
A | G | 10 | a0001c0001t0003g0187a0001c0001t0003g0191a0001c0001t0003g0192others(7): Show | 10 | HG00558.hp2 HG01081.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1138-6386A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753864 | ||||||
| chr6:109753871
|
C | G | 3 | a0001c0001t0003g0001a0001c0001t0003g0162a0001c0001t0003g0168 | 4 | NA18960.hp2 NA18968.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-6379C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753871 | ||||||
| chr6:109753913
|
G | T | 1 | a0002c0002t0001g0154 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1138-6337G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753913 | ||||||
| chr6:109753920
|
A | G | 1 | a0001c0003t0001g0060 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1138-6330A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753920 | ||||||
| chr6:109753996
|
G | T | 152 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(149): Show | 153 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1138-6254G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753996 | ||||||
| chr6:109754152
|
G | A | 1 | a0002c0002t0002g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1138-6098G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754152 | ||||||
| chr6:109754165
|
C | G | 57 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(54): Show | 57 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1138-6085C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754165 | ||||||
| chr6:109754271
|
T | G | 1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1138-5979T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754271 | ||||||
| chr6:109754312
|
C | G | 2 | a0002c0002t0001g0152a0002c0002t0001g0154 | 2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1138-5938C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754312 | ||||||
| chr6:109754390
|
G | T | 2 | a0001c0003t0001g0177a0002c0004t0001g0189 | 2 | HG01934.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1138-5860G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754390 | ||||||
| chr6:109754463
|
T | G | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1138-5787T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754463 | ||||||
| chr6:109754475
|
A | C | 3 | a0001c0003t0001g0257a0001c0003t0001g0258a0001c0003t0001g0259 | 3 | HG01069.hp2 HG01071.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1138-5775A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754475 | ||||||
| chr6:109754491
|
A | G | 2 | a0002c0002t0004g0355a0002c0002t0004g0357 | 2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1138-5759A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754491 | ||||||
| chr6:109754638
|
G | C | 1 | a0002c0004t0001g0216 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1138-5612G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754638 | ||||||
| chr6:109754653
|
C | T | 67 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(64): Show | 68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1138-5597C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754653 | ||||||
| chr6:109754672
|
G | C | 46 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(43): Show | 46 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1138-5578G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754672 | ||||||
| chr6:109754725
|
C | T | 67 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(64): Show | 68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1138-5525C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754725 | ||||||
| chr6:109754787
|
T | A | 3 | a0001c0001t0003g0364a0001c0001t0003g0365a0001c0001t0003g0366 | 3 | HG02615.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1138-5463T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754787 | ||||||
| chr6:109754865
|
G | A | 2 | a0002c0004t0001g0215a0002c0004t0001g0216 | 2 | HG01346.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1138-5385G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754865 | ||||||
| chr6:109754945
|
G | A | 4 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127others(1): Show | 4 | HG03453.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-5305G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754945 | ||||||
| chr6:109754974
|
T | G | 3 | a0002c0002t0001g0153a0002c0004t0001g0215a0002c0004t0001g0216 | 3 | HG00323.hp2 HG01346.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1138-5276T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754974 | ||||||
| chr6:109755032
|
G | T | 2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1138-5218G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755032 | ||||||
| chr6:109755147
|
C | T | 3 | a0001c0003t0001g0302a0001c0003t0001g0319a0001c0003t0001g0368 | 3 | HG01346.hp2 NA18969.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1138-5103C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755147 | ||||||
| chr6:109755148
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1138-5102G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755148 | ||||||
| chr6:109755191
|
T | C | 2 | a0001c0003t0001g0034a0001c0003t0001g0035 | 2 | NA19002.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1138-5059T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755191 | ||||||
| chr6:109755195
|
C | T | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-5055C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755195 | ||||||
| chr6:109755268
|
G | C | 1 | a0003c0005t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1138-4982G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755268 | ||||||
| chr6:109755413
|
G | A | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1138-4837G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755413 | ||||||
| chr6:109755613
|
T | G | 2 | a0001c0001t0002g0065a0002c0004t0001g0064 | 2 | HG01169.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1138-4637T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755613 | ||||||
| chr6:109755614
|
G | A | 3 | a0001c0001t0002g0122a0001c0001t0002g0124a0002c0002t0004g0123 | 3 | HG02622.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1138-4636G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755614 | ||||||
| chr6:109755661
|
T | C | 2 | a0002c0002t0002g0362a0002c0002t0002g0363 | 2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1138-4589T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755661 | ||||||
| chr6:109755729
|
A | G | 1 | a0001c0001t0002g0213 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1138-4521A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755729 | ||||||
| chr6:109755820
|
C | T | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1138-4430C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755820 | ||||||
| chr6:109755878
|
T | G | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | HG00423.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1138-4372T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755878 | ||||||
| chr6:109755957
|
G | A | 13 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(10): Show | 13 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1138-4293G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755957 | ||||||
| chr6:109755994
|
T | C | 46 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(43): Show | 46 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1138-4256T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755994 | ||||||
| chr6:109756003
|
C | T | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138-4247C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756003 | ||||||
| chr6:109756083
|
C | T | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1138-4167C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756083 | ||||||
| chr6:109756118
|
T | G | 277 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(274): Show | 279 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.1138-4132T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756118 | ||||||
| chr6:109756167
|
A | G | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-4083A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756167 | ||||||
| chr6:109756187
|
T | C | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-4063T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756187 | ||||||
| chr6:109756188
|
A | T | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-4062A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756188 | ||||||
| chr6:109756189
|
C | G | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-4061C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756189 | ||||||
| chr6:109756264
|
C | A | 1 | a0002c0004t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1138-3986C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756264 | ||||||
| chr6:109756305
|
C | T | 48 | a0003c0005t0001g0002a0003c0005t0001g0068a0003c0005t0001g0249others(45): Show | 49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.1138-3945C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756305 | ||||||
| chr6:109756306
|
A | G | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-3944A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756306 | ||||||
| chr6:109756340
|
C | G | 1 | a0002c0004t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1138-3910C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756340 | ||||||
| chr6:109756449
|
T | C | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-3801T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756449 | ||||||
| chr6:109756474
|
A | G | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-3776A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756474 | ||||||
| chr6:109756475
|
T | C | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-3775T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756475 | ||||||
| chr6:109756668
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1138-3582C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756668 | ||||||
| chr6:109756669
|
G | A | 19 | a0001c0001t0003g0001a0001c0001t0003g0162a0001c0001t0003g0163others(16): Show | 20 | HG00438.hp1 HG03041.hp2 NA18939.hp1 others(17): Show |
intron_variant | MODIFIER | c.1138-3581G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756669 | ||||||
| chr6:109756766
|
A | G | 3 | a0002c0002t0002g0139a0002c0002t0002g0150a0002c0004t0001g0140 | 3 | NA19007.hp2 NA19063.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1138-3484A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756766 | ||||||
| chr6:109756912
|
G | A | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1138-3338G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756912 | ||||||
| chr6:109756958
|
G | C | 2 | a0002c0002t0002g0084a0002c0002t0002g0085 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1138-3292G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756958 | ||||||
| chr6:109756959
|
C | G | 4 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127others(1): Show | 4 | HG03453.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-3291C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756959 | ||||||
| chr6:109757021
|
T | C | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1138-3229T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757021 | ||||||
| chr6:109757026
|
G | A | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1138-3224G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757026 | ||||||
| chr6:109757067
|
C | T | 2 | a0002c0004t0001g0128a0002c0004t0001g0129 | 2 | HG01255.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1138-3183C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757067 | ||||||
| chr6:109757072
|
A | G | 4 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(1): Show | 4 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-3178A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757072 | ||||||
| chr6:109757078
|
G | C | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1138-3172G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757078 | ||||||
| chr6:109757178
|
GT | G | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1138-3067delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109757178 | |||||
| chr6:109757508
|
A | T | 1 | a0001c0001t0003g0185 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1138-2742A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757508 | ||||||
| chr6:109757634
|
A | T | 1 | a0002c0014t0002g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1138-2616A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757634 | ||||||
| chr6:109757794
|
T | G | 1 | a0002c0002t0004g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1138-2456T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757794 | ||||||
| chr6:109757832
|
C | G | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1138-2418C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757832 | ||||||
| chr6:109757908
|
A | G | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1138-2342A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757908 | ||||||
| chr6:109757955
|
AAG | A | 3 | a0001c0003t0001g0296a0001c0003t0001g0302a0001c0003t0001g0303 | 3 | HG01346.hp2 HG01361.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1138-2290_1138-228 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109757955 | |||||
| chr6:109758261
|
C | T | 273 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(270): Show | 275 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.1138-1989C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109758261 | ||||||
| chr6:109758416
|
A | C | 3 | a0003c0005t0001g0249a0003c0005t0001g0350a0003c0017t0001g0314 | 3 | NA18943.hp1 NA18959.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1138-1834A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109758416 | ||||||
| chr6:109758422
|
T | TGG | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1138-1827_1138-182 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109758422 | |||||
| chr6:109758524
|
A | G | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-1726A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109758524 | ||||||
| chr6:109758787
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1138-1463G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109758787 | ||||||
| chr6:109758915
|
G | A | 1 | a0002c0002t0002g0010 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1138-1335G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109758915 | ||||||
| chr6:109759098
|
G | T | 1 | a0001c0001t0002g0100 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1138-1152G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759098 | ||||||
| chr6:109759194
|
C | T | 6 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(3): Show | 6 | NA18947.hp2 NA18949.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1138-1056C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759194 | ||||||
| chr6:109759239
|
A | G | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-1011A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759239 | ||||||
| chr6:109759264
|
C | T | 1 | a0002c0002t0002g0069 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1138-986C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759264 | ||||||
| chr6:109759268
|
A | T | 3 | a0002c0002t0001g0143a0002c0002t0001g0144a0002c0002t0001g0148 | 3 | NA18955.hp2 NA18998.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1138-982A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759268 | ||||||
| chr6:109759354
|
T | C | 151 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(148): Show | 152 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1138-896T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759354 | ||||||
| chr6:109759417
|
GA | G | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138-824delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109759417 | |||||
| chr6:109759426
|
A | C | 28 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0133others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1138-824A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759426 | ||||||
| chr6:109759443
|
T | A | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1138-807T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759443 | ||||||
| chr6:109759549
|
C | T | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-701C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759549 | ||||||
| chr6:109759565
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0002g0017 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1138-685G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759565 | ||||||
| chr6:109759799
|
G | A | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138-451G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759799 | ||||||
| chr6:109759959
|
G | A | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-291G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759959 | ||||||
| chr6:109759966
|
A | G | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-284A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759966 | ||||||
| chr6:109759998
|
G | A | 2 | a0004c0008t0002g0309a0004c0008t0002g0322 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1138-252G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759998 | ||||||
| chr6:109760075
|
G | T | 15 | a0001c0001t0002g0198a0002c0002t0002g0164a0002c0002t0004g0196others(12): Show | 15 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1138-175G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109760075 | ||||||
| chr6:109760135
|
G | C | 1 | a0002c0004t0001g0051 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1138-115G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109760135 | ||||||
| chr6:109760205
|
A | T | 1 | a0002c0004t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1138-45A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109760205 | ||||||
| chr6:109760228
|
A | G | 1 | a0003c0005t0001g0349 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1138-22A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109760228 | ||||||
| chr6:109760415
|
G | A | 109 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(106): Show | 110 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1271+32G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109760415 | ||||||
| chr6:109760821
|
C | T | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1271+438C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109760821 | ||||||
| chr6:109760879
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1271+496C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109760879 | ||||||
| chr6:109760919
|
G | A | 48 | a0003c0005t0001g0002a0003c0005t0001g0068a0003c0005t0001g0249others(45): Show | 49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.1271+536G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109760919 | ||||||
| chr6:109761361
|
T | G | 1 | a0002c0002t0001g0133 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1272-730T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109761361 | ||||||
| chr6:109761736
|
C | T | 6 | a0001c0001t0002g0221a0001c0001t0002g0223a0001c0001t0002g0224others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1272-355C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109761736 | ||||||
| chr6:109761853
|
C | T | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1272-238C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109761853 | ||||||
| chr6:109762585
|
A | G | 1 | a0002c0002t0004g0354 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1388+378A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109762585 | ||||||
| chr6:109762622
|
G | A | 1 | a0002c0002t0004g0204 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1388+415G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109762622 | ||||||
| chr6:109762861
|
A | G | 53 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(50): Show | 53 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1388+654A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109762861 | ||||||
| chr6:109762875
|
C | T | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1388+668C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109762875 | ||||||
| chr6:109762876
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1388+669G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109762876 | ||||||
| chr6:109762950
|
G | A | 1 | a0002c0002t0004g0355 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1388+743G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109762950 | ||||||
| chr6:109763001
|
G | T | 1 | a0005c0019t0006g0016 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1388+794G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109763001 | ||||||
| chr6:109763103
|
C | G | 1 | a0004c0006t0001g0308 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1389-834C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109763103 | ||||||
| chr6:109763331
|
G | A | 119 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(116): Show | 120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1389-606G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109763331 | ||||||
| chr6:109763402
|
T | A | 152 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(149): Show | 153 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1389-535T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109763402 | ||||||
| chr6:109763406
|
TC | T | 152 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(149): Show | 153 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1389-530delC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109763406 | ||||||
| chr6:109763767
|
A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1389-170A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109763767 | ||||||
| chr6:109764036
|
G | A | 9 | a0001c0001t0002g0279a0001c0003t0001g0003a0001c0003t0001g0004others(6): Show | 9 | HG02602.hp1 HG04184.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1434+54G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764036 | ||||||
| chr6:109764054
|
A | G | 68 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(65): Show | 69 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.1434+72A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764054 | ||||||
| chr6:109764140
|
A | T | 1 | a0002c0002t0004g0357 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1434+158A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764140 | ||||||
| chr6:109764163
|
G | T | 53 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(50): Show | 53 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1434+181G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764163 | ||||||
| chr6:109764211
|
G | A | 1 | a0001c0001t0003g0366 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1434+229G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764211 | ||||||
| chr6:109764220
|
T | C | 278 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(275): Show | 280 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.1434+238T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764220 | ||||||
| chr6:109764235
|
G | A | 1 | a0001c0003t0001g0021 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1434+253G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764235 | ||||||
| chr6:109764305
|
G | A | 2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1434+323G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764305 | ||||||
| chr6:109764443
|
GA | G | 223 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(220): Show | 225 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.1434+475delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr6 | 109764443 | |||||
| chr6:109764719
|
A | G | 3 | a0001c0003t0001g0021a0001c0003t0001g0031a0001c0003t0001g0033 | 3 | HG02015.hp2 HG02056.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1435-294A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764719 | ||||||
| chr6:109764723
|
A | G | 1 | a0001c0001t0003g0179 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1435-290A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764723 | ||||||
| chr6:109764757
|
T | C | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1435-256T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764757 | ||||||
| chr6:109764895
|
T | TTTTTTG | 10 | a0001c0003t0001g0284a0001c0003t0001g0285a0001c0003t0001g0286others(7): Show | 10 | HG01081.hp1 HG01175.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1435-84_1435-79dup others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr6 | 109764895 | |||||
| chr6:109764895
|
T | TTTTTTGT others(5): Show |
50 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(47): Show | 50 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1435-90_1435-79dup others(12): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr6 | 109764895 | |||||
| chr6:109764895
|
TTTTTTG | T | 67 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(64): Show | 68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1435-84_1435-79del others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr6 | 109764895 | |||||
| chr6:109764895
|
TTTTTTGT others(5): Show |
T | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1435-90_1435-79del others(12): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr6 | 109764895 | |||||
| chr6:109764895
|
TTTTTTGT others(11): Show |
T | 1 | a0001c0001t0003g0185 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1435-96_1435-79del others(18): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr6 | 109764895 | |||||
| chr6:109766412
|
T | C | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1584-317T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 14/22 | chr6 | 109766412 | ||||||
| chr6:109766414
|
G | A | 68 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(65): Show | 69 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.1584-315G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 14/22 | chr6 | 109766414 | ||||||
| chr6:109766645
|
T | A | 68 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(65): Show | 69 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.1584-84T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 14/22 | chr6 | 109766645 | ||||||
| chr6:109766699
|
A | C | 4 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0002g0008others(1): Show | 4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1584-30A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 14/22 | chr6 | 109766699 | ||||||
| chr6:109766916
|
A | G | 1 | a0002c0004t0001g0089 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1750+21A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109766916 | ||||||
| chr6:109766950
|
A | G | 1 | a0001c0001t0002g0290 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1750+55A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109766950 | ||||||
| chr6:109767116
|
T | A | 1 | a0001c0001t0002g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1750+221T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767116 | ||||||
| chr6:109767247
|
G | A | 1 | a0002c0002t0003g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1750+352G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767247 | ||||||
| chr6:109767454
|
G | T | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1750+559G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767454 | ||||||
| chr6:109767525
|
T | C | 1 | a0002c0004t0001g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1750+630T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767525 | ||||||
| chr6:109767596
|
C | T | 15 | a0001c0001t0002g0198a0002c0002t0002g0164a0002c0002t0004g0196others(12): Show | 15 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1750+701C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767596 | ||||||
| chr6:109767636
|
C | T | 6 | a0001c0001t0002g0221a0001c0001t0002g0223a0001c0001t0002g0224others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1750+741C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767636 | ||||||
| chr6:109767707
|
A | G | 1 | a0002c0002t0004g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1750+812A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767707 | ||||||
| chr6:109767842
|
A | T | 1 | a0003c0007t0001g0328 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1750+947A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767842 | ||||||
| chr6:109767850
|
C | T | 47 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(44): Show | 47 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1750+955C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767850 | ||||||
| chr6:109767871
|
C | T | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1750+976C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767871 | ||||||
| chr6:109767939
|
G | A | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1750+1044G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767939 | ||||||
| chr6:109768389
|
A | G | 1 | a0002c0002t0004g0197 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1750+1494A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768389 | ||||||
| chr6:109768445
|
G | A | 14 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(11): Show | 14 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1750+1550G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768445 | ||||||
| chr6:109768601
|
C | T | 1 | a0001c0001t0002g0361 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1750+1706C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768601 | ||||||
| chr6:109768732
|
C | T | 6 | a0001c0003t0001g0145a0001c0003t0001g0263a0001c0003t0001g0264others(3): Show | 6 | HG00408.hp2 HG02074.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1750+1837C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768732 | ||||||
| chr6:109768789
|
A | C | 274 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(271): Show | 276 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.1750+1894A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768789 | ||||||
| chr6:109768846
|
C | G | 62 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(59): Show | 63 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(60): Show |
intron_variant | MODIFIER | c.1750+1951C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768846 | ||||||
| chr6:109768874
|
T | G | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1750+1979T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768874 | ||||||
| chr6:109768885
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1750+1990C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768885 | ||||||
| chr6:109769087
|
C | T | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1750+2192C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109769087 | ||||||
| chr6:109769107
|
C | CT | 149 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(146): Show | 150 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.1750+2226dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109769107 | |||||
| chr6:109769144
|
A | C | 274 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(271): Show | 276 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.1750+2249A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109769144 | ||||||
| chr6:109769793
|
C | A | 1 | a0002c0002t0004g0207 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1750+2898C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109769793 | ||||||
| chr6:109769827
|
C | G | 278 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(275): Show | 280 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.1750+2932C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109769827 | ||||||
| chr6:109769861
|
G | C | 95 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(92): Show | 95 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1750+2966G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109769861 | ||||||
| chr6:109770007
|
G | A | 11 | a0001c0001t0002g0304a0001c0003t0001g0291a0001c0003t0001g0292others(8): Show | 11 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1750+3112G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770007 | ||||||
| chr6:109770252
|
C | T | 1 | a0003c0005t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1750+3357C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770252 | ||||||
| chr6:109770347
|
G | A | 2 | a0001c0001t0002g0081a0001c0003t0001g0060 | 2 | HG03017.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1750+3452G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770347 | ||||||
| chr6:109770359
|
GTA | G | 3 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0014t0002g0011 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1750+3472_1750+347 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109770359 | |||||
| chr6:109770361
|
A | G | 28 | a0001c0001t0003g0001a0001c0001t0003g0162a0001c0001t0003g0163others(25): Show | 29 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1750+3466A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770361 | ||||||
| chr6:109770416
|
T | C | 1 | a0001c0003t0001g0145 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1750+3521T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770416 | ||||||
| chr6:109770564
|
T | A | 2 | a0002c0002t0001g0141a0002c0002t0001g0142 | 2 | NA19004.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1750+3669T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770564 | ||||||
| chr6:109770851
|
G | T | 109 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(106): Show | 110 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1750+3956G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770851 | ||||||
| chr6:109770868
|
G | A | 1 | a0002c0004t0001g0051 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1750+3973G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770868 | ||||||
| chr6:109770901
|
TC | T | 4 | a0002c0002t0002g0211a0002c0009t0002g0157a0002c0009t0002g0158others(1): Show | 4 | HG02109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1750+4009delC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109770901 | |||||
| chr6:109771461
|
C | CT | 108 | a0001c0001t0002g0015a0001c0001t0002g0042a0001c0001t0002g0059others(105): Show | 109 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1750+4591dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109771461 | |||||
| chr6:109771461
|
C | CTT | 64 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(61): Show | 64 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.1750+4590_1750+459 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109771461 | |||||
| chr6:109771461
|
C | CTTT | 10 | a0001c0001t0003g0366a0001c0003t0001g0004a0001c0003t0001g0251others(7): Show | 10 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1750+4589_1750+459 others(7): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109771461 | |||||
| chr6:109771461
|
CTT | C | 8 | a0001c0001t0002g0214a0001c0001t0003g0162a0001c0001t0003g0195others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1750+4590_1750+459 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109771461 | |||||
| chr6:109771461
|
CTTT | C | 99 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(96): Show | 100 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1750+4589_1750+459 others(7): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109771461 | |||||
| chr6:109771499
|
C | T | 24 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0217others(21): Show | 24 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1750+4604C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771499 | ||||||
| chr6:109771500
|
G | C | 2 | a0003c0005t0001g0337a0003c0005t0001g0338 | 2 | NA19063.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1750+4605G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771500 | ||||||
| chr6:109771538
|
G | T | 4 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0002g0008others(1): Show | 4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1750+4643G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771538 | ||||||
| chr6:109771559
|
C | T | 33 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1750+4664C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771559 | ||||||
| chr6:109771593
|
C | T | 67 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(64): Show | 68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1750+4698C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771593 | ||||||
| chr6:109771697
|
C | A | 204 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(201): Show | 205 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.1750+4802C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771697 | ||||||
| chr6:109771716
|
G | A | 1 | a0002c0002t0003g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1750+4821G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771716 | ||||||
| chr6:109771974
|
C | T | 1 | a0003c0017t0001g0314 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1751-4948C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771974 | ||||||
| chr6:109772097
|
A | G | 2 | a0001c0001t0002g0065a0002c0004t0001g0064 | 2 | HG01169.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1751-4825A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772097 | ||||||
| chr6:109772418
|
G | A | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751-4504G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772418 | ||||||
| chr6:109772494
|
T | C | 3 | a0001c0003t0001g0257a0001c0003t0001g0258a0001c0003t0001g0259 | 3 | HG01069.hp2 HG01071.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1751-4428T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772494 | ||||||
| chr6:109772645
|
G | T | 42 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(39): Show | 42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1751-4277G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772645 | ||||||
| chr6:109772652
|
C | T | 1 | a0002c0002t0002g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1751-4270C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772652 | ||||||
| chr6:109772681
|
G | A | 62 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(59): Show | 63 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(60): Show |
intron_variant | MODIFIER | c.1751-4241G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772681 | ||||||
| chr6:109772836
|
G | A | 66 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(63): Show | 67 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(64): Show |
intron_variant | MODIFIER | c.1751-4086G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772836 | ||||||
| chr6:109773356
|
A | T | 1 | a0001c0003t0001g0060 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1751-3566A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773356 | ||||||
| chr6:109773413
|
A | T | 1 | a0003c0005t0001g0346 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1751-3509A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773413 | ||||||
| chr6:109773423
|
C | T | 95 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(92): Show | 95 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1751-3499C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773423 | ||||||
| chr6:109773520
|
C | T | 1 | a0002c0015t0001g0181 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1751-3402C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773520 | ||||||
| chr6:109773612
|
C | T | 1 | a0001c0003t0001g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1751-3310C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773612 | ||||||
| chr6:109773624
|
C | T | 3 | a0001c0001t0002g0015a0001c0001t0002g0017a0005c0019t0006g0016 | 3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1751-3298C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773624 | ||||||
| chr6:109773880
|
C | A | 1 | a0003c0005t0001g0343 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1751-3042C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773880 | ||||||
| chr6:109773897
|
C | T | 1 | a0002c0002t0002g0007 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1751-3025C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773897 | ||||||
| chr6:109774460
|
G | A | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1751-2462G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774460 | ||||||
| chr6:109774526
|
A | C | 2 | a0001c0001t0002g0065a0002c0004t0001g0064 | 2 | HG01169.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1751-2396A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774526 | ||||||
| chr6:109774542
|
T | G | 4 | a0002c0002t0002g0083a0002c0002t0002g0084a0002c0002t0002g0085others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751-2380T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774542 | ||||||
| chr6:109774624
|
T | C | 1 | a0003c0005t0001g0068 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1751-2298T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774624 | ||||||
| chr6:109774743
|
G | A | 12 | a0002c0002t0002g0110a0002c0002t0002g0111a0002c0002t0002g0112others(9): Show | 12 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.1751-2179G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774743 | ||||||
| chr6:109774799
|
T | C | 1 | a0003c0005t0001g0320 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1751-2123T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774799 | ||||||
| chr6:109774830
|
C | G | 3 | a0002c0002t0005g0125a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1751-2092C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774830 | ||||||
| chr6:109774850
|
A | G | 278 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0198others(275): Show | 280 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.1751-2072A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774850 | ||||||
| chr6:109774914
|
G | A | 4 | a0002c0002t0002g0211a0002c0009t0002g0157a0002c0009t0002g0158others(1): Show | 4 | HG02109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1751-2008G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774914 | ||||||
| chr6:109775517
|
G | C | 8 | a0001c0001t0002g0221a0001c0001t0002g0223a0001c0001t0002g0224others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1751-1405G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109775517 | ||||||
| chr6:109775564
|
C | T | 2 | a0001c0003t0001g0281a0001c0003t0001g0282 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1751-1358C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109775564 | ||||||
| chr6:109775693
|
T | C | 53 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(50): Show | 53 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1751-1229T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109775693 | ||||||
| chr6:109775700
|
A | G | 14 | a0001c0001t0002g0299a0001c0001t0002g0304a0001c0003t0001g0291others(11): Show | 14 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1751-1222A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109775700 | ||||||
| chr6:109775759
|
C | T | 2 | a0001c0003t0001g0300a0001c0003t0001g0301 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1751-1163C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109775759 | ||||||
| chr6:109775876
|
A | G | 6 | a0001c0001t0002g0198a0002c0002t0004g0196a0002c0002t0005g0125others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1751-1046A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109775876 | ||||||
| chr6:109776039
|
G | A | 2 | a0001c0001t0002g0214a0001c0001t0002g0239 | 2 | HG01109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1751-883G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776039 | ||||||
| chr6:109776060
|
A | G | 1 | a0001c0003t0001g0274 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1751-862A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776060 | ||||||
| chr6:109776179
|
T | C | 1 | a0002c0002t0001g0151 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1751-743T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776179 | ||||||
| chr6:109776214
|
G | A | 5 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(2): Show | 5 | HG02615.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1751-708G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776214 | ||||||
| chr6:109776585
|
A | T | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0012others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1751-337A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776585 | ||||||
| chr6:109776588
|
T | A | 10 | a0001c0001t0002g0221a0001c0001t0002g0223a0001c0001t0002g0224others(7): Show | 10 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1751-334T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776588 | ||||||
| chr6:109776612
|
G | A | 1 | a0001c0001t0002g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1751-310G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776612 | ||||||
| chr6:109776628
|
A | G | 3 | a0002c0009t0002g0157a0002c0009t0002g0158a0002c0009t0002g0159 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1751-294A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776628 | ||||||
| chr6:109776670
|
A | G | 1 | a0002c0002t0004g0229 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1751-252A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776670 | ||||||
| chr6:109776806
|
G | A | 1 | a0001c0001t0003g0167 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1751-116G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776806 | ||||||
| chr6:109776847
|
C | T | 1 | a0002c0002t0001g0136 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1751-75C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776847 | ||||||
| chr6:109777184
|
A | T | 1 | a0002c0002t0002g0119 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1889+124A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777184 | ||||||
| chr6:109777362
|
T | G | 1 | a0004c0006t0001g0308 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1889+302T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777362 | ||||||
| chr6:109777670
|
G | T | 43 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(40): Show | 43 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1889+610G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777670 | ||||||
| chr6:109777707
|
C | T | 4 | a0002c0002t0002g0005a0002c0002t0002g0007a0002c0002t0002g0008others(1): Show | 4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1889+647C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777707 | ||||||
| chr6:109777723
|
G | C | 1 | a0001c0001t0002g0213 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1889+663G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777723 | ||||||
| chr6:109777938
|
A | G | 1 | a0002c0002t0001g0358 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1889+878A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777938 | ||||||
| chr6:109777947
|
A | T | 1 | a0002c0002t0004g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1889+887A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777947 | ||||||
| chr6:109777994
|
A | C | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1889+934A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777994 | ||||||
| chr6:109778078
|
C | G | 63 | a0001c0001t0002g0122a0001c0001t0002g0124a0001c0001t0002g0221others(60): Show | 64 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.1889+1018C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778078 | ||||||
| chr6:109778163
|
G | A | 2 | a0001c0003t0001g0252a0002c0002t0004g0228 | 2 | HG02809.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1889+1103G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778163 | ||||||
| chr6:109778182
|
C | T | 44 | a0001c0001t0002g0122a0001c0001t0003g0001a0001c0001t0003g0162others(41): Show | 45 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1889+1122C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778182 | ||||||
| chr6:109778183
|
G | A | 41 | a0001c0001t0002g0198a0001c0001t0002g0213a0001c0001t0002g0214others(38): Show | 41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1889+1123G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778183 | ||||||
| chr6:109778298
|
T | TA | 69 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0268others(66): Show | 69 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.1889+1252dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109778298 | |||||
| chr6:109778363
|
G | A | 13 | a0001c0001t0002g0198a0002c0002t0002g0211a0002c0002t0004g0196others(10): Show | 13 | HG02109.hp1 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1889+1303G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778363 | ||||||
| chr6:109778470
|
C | CA | 287 | a0001c0001t0002g0052a0001c0001t0002g0081a0001c0001t0002g0095others(284): Show | 289 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(286): Show |
intron_variant | MODIFIER | c.1889+1423dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109778470 | |||||
| chr6:109778611
|
T | G | 1 | a0001c0001t0002g0100 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1889+1551T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778611 | ||||||
| chr6:109778632
|
T | C | 40 | a0001c0001t0002g0052a0001c0001t0002g0213a0001c0001t0002g0214others(37): Show | 40 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1889+1572T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778632 | ||||||
| chr6:109778699
|
C | T | 2 | a0001c0001t0002g0081a0001c0003t0001g0060 | 2 | HG03017.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1889+1639C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778699 | ||||||
| chr6:109778715
|
C | T | 1 | a0004c0006t0001g0344 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1889+1655C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778715 | ||||||
| chr6:109778744
|
G | A | 20 | a0001c0003t0001g0278a0002c0002t0001g0132a0002c0002t0001g0134others(17): Show | 20 | HG00544.hp2 HG00738.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.1889+1684G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778744 | ||||||
| chr6:109778755
|
T | C | 5 | a0001c0001t0002g0030a0001c0003t0001g0296a0001c0003t0001g0297others(2): Show | 5 | HG01106.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1889+1695T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778755 | ||||||
| chr6:109778790
|
G | A | 327 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(324): Show | 329 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.1889+1730G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778790 | ||||||
| chr6:109778809
|
T | C | 100 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0019others(97): Show | 101 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1889+1749T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778809 | ||||||
| chr6:109778812
|
G | A | 2 | a0002c0002t0002g0362a0002c0002t0002g0363 | 2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1889+1752G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778812 | ||||||
| chr6:109778813
|
G | A | 362 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(359): Show | 364 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(361): Show |
intron_variant | MODIFIER | c.1889+1753G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778813 | ||||||
| chr6:109778815
|
G | A | 46 | a0001c0001t0002g0045a0001c0001t0002g0070a0001c0001t0002g0105others(43): Show | 46 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(43): Show |
intron_variant | MODIFIER | c.1889+1755G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778815 | ||||||
| chr6:109778820
|
T | C | 12 | a0001c0003t0001g0276a0002c0002t0002g0362a0002c0002t0002g0363others(9): Show | 12 | HG01081.hp1 HG01243.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1889+1760T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778820 | ||||||
| chr6:109778830
|
C | A | 8 | a0002c0002t0002g0084a0002c0002t0002g0085a0002c0002t0002g0362others(5): Show | 8 | HG01255.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1889+1770C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778830 | ||||||
| chr6:109778841
|
T | C | 12 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1889+1781T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778841 | ||||||
| chr6:109778842
|
G | C | 2 | a0002c0002t0002g0362a0002c0002t0002g0363 | 2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1889+1782G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778842 | ||||||
| chr6:109778846
|
G | A | 2 | a0002c0002t0002g0362a0002c0002t0002g0363 | 2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1889+1786G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778846 | ||||||
| chr6:109778848
|
C | T | 2 | a0002c0004t0001g0219a0002c0004t0001g0220 | 2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1889+1788C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778848 | ||||||
| chr6:109778850
|
T | C | 2 | a0002c0002t0002g0362a0002c0002t0002g0363 | 2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1889+1790T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778850 | ||||||
| chr6:109778879
|
G | A | 15 | a0001c0001t0002g0052a0001c0001t0002g0213a0001c0001t0002g0214others(12): Show | 15 | HG00099.hp2 HG00735.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1889+1819G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778879 | ||||||
| chr6:109778881
|
G | C | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1889+1821G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778881 | ||||||
| chr6:109778884
|
C | T | 6 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0269others(3): Show | 6 | HG03927.hp2 NA18943.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1889+1824C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778884 | ||||||
| chr6:109778889
|
G | A | 2 | a0001c0001t0002g0025a0002c0002t0001g0218 | 2 | NA19010.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1889+1829G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778889 | ||||||
| chr6:109778891
|
G | A | 1 | a0002c0004t0001g0205 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1889+1831G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778891 | ||||||
| chr6:109778896
|
G | T | 1 | a0001c0001t0002g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1889+1836G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778896 | ||||||
| chr6:109778921
|
T | C | 3 | a0003c0005t0001g0329a0003c0005t0001g0330a0003c0005t0001g0331 | 3 | HG02074.hp2 NA18952.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1889+1861T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778921 | ||||||
| chr6:109778999
|
A | G | 77 | a0001c0001t0002g0104a0001c0001t0003g0001a0001c0001t0003g0022others(74): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1889+1939A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778999 | ||||||
| chr6:109779023
|
T | A | 2 | a0001c0001t0002g0015a0001c0001t0002g0017 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1889+1963T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109779023 | ||||||
| chr6:109779130
|
C | G | 1 | a0003c0005t0001g0337 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1889+2070C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109779130 | ||||||
| chr6:109779140
|
T | G | 1 | a0003c0005t0001g0337 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1889+2080T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109779140 | ||||||
| chr6:109779272
|
A | G | 60 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(57): Show | 62 | HG00639.hp1 HG01175.hp2 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.1889+2212A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109779272 | ||||||
| chr6:109779521
|
G | A | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1889+2461G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109779521 | ||||||
| chr6:109779834
|
G | A | 2 | a0001c0001t0003g0179a0004c0008t0002g0315 | 2 | HG01496.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.1889+2774G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109779834 | ||||||
| chr6:109780177
|
G | C | 1 | a0002c0002t0002g0069 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1889+3117G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780177 | ||||||
| chr6:109780207
|
G | A | 1 | a0008c0011t0001g0367 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1889+3147G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780207 | ||||||
| chr6:109780220
|
C | G | 1 | a0001c0003t0001g0271 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1889+3160C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780220 | ||||||
| chr6:109780297
|
T | C | 17 | a0001c0001t0003g0187a0001c0003t0001g0024a0001c0003t0001g0170others(14): Show | 17 | HG01081.hp2 HG01256.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1889+3237T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780297 | ||||||
| chr6:109780353
|
C | T | 1 | a0001c0001t0002g0100 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1889+3293C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780353 | ||||||
| chr6:109780593
|
A | C | 3 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0014t0002g0011 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1889+3533A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780593 | ||||||
| chr6:109780782
|
A | G | 1 | a0002c0002t0004g0352 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1889+3722A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780782 | ||||||
| chr6:109780955
|
T | C | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1889+3895T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780955 | ||||||
| chr6:109781107
|
C | T | 3 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0014t0002g0011 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1890-3863C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781107 | ||||||
| chr6:109781317
|
C | T | 1 | a0001c0003t0001g0293 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1890-3653C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781317 | ||||||
| chr6:109781331
|
C | G | 1 | a0002c0002t0002g0363 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1890-3639C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781331 | ||||||
| chr6:109781366
|
T | C | 2 | a0003c0005t0001g0329a0003c0005t0001g0330 | 2 | HG02074.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1890-3604T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781366 | ||||||
| chr6:109781398
|
C | A | 110 | a0001c0001t0002g0046a0001c0001t0002g0052a0001c0001t0002g0213others(107): Show | 110 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1890-3572C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781398 | ||||||
| chr6:109781425
|
A | G | 29 | a0001c0003t0001g0044a0001c0003t0001g0145a0001c0003t0001g0251others(26): Show | 29 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1890-3545A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781425 | ||||||
| chr6:109781718
|
A | G | 2 | a0002c0009t0002g0157a0002c0009t0002g0159 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1890-3252A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781718 | ||||||
| chr6:109781773
|
C | CAGATTTT others(270): Show |
1 | a0001c0003t0001g0275 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(281): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(271): Show |
1 | a0001c0003t0001g0274 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(282): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(272): Show |
1 | a0001c0003t0001g0173 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(283): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(275): Show |
1 | a0001c0001t0002g0289 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(286): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(277): Show |
1 | a0001c0003t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(288): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(278): Show |
1 | a0001c0003t0001g0188 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(289): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(279): Show |
2 | a0001c0003t0001g0033a0001c0003t0001g0175 | 2 | HG02015.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(290): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(280): Show |
8 | a0001c0001t0002g0217a0001c0003t0001g0043a0001c0003t0001g0258others(5): Show | 8 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(291): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(281): Show |
4 | a0001c0003t0001g0044a0001c0003t0001g0271a0001c0003t0001g0280others(1): Show | 4 | HG00735.hp2 HG02486.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(292): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(282): Show |
3 | a0001c0003t0001g0034a0001c0003t0001g0165a0001c0003t0001g0263 | 3 | HG02074.hp1 NA18953.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(293): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(283): Show |
2 | a0001c0003t0001g0035a0001c0003t0001g0166 | 2 | NA19002.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(294): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(284): Show |
1 | a0001c0003t0001g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(295): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(285): Show |
1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(296): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(286): Show |
1 | a0001c0003t0001g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(297): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(287): Show |
1 | a0004c0008t0002g0309 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(298): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(287): Show |
3 | a0001c0003t0001g0243a0001c0003t0001g0253a0004c0006t0001g0339 | 3 | HG00099.hp2 NA18961.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(298): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(288): Show |
1 | a0004c0008t0002g0322 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(299): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(288): Show |
2 | a0001c0003t0001g0003a0001c0003t0001g0004 | 2 | NA18943.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(299): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(289): Show |
2 | a0001c0003t0001g0297a0001c0003t0001g0302 | 2 | HG01346.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(300): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(290): Show |
4 | a0001c0001t0002g0304a0001c0003t0001g0296a0001c0003t0001g0303others(1): Show | 4 | HG01361.hp1 HG01517.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(301): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(291): Show |
3 | a0002c0002t0002g0084a0002c0002t0002g0085a0005c0019t0006g0016 | 3 | HG02886.hp2 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(302): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(292): Show |
1 | a0002c0002t0002g0083 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(303): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(293): Show |
1 | a0001c0001t0002g0241 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(304): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(294): Show |
2 | a0001c0001t0002g0227a0004c0006t0001g0307 | 2 | HG01169.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(305): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(297): Show |
2 | a0001c0003t0001g0293a0002c0002t0002g0009 | 2 | HG02280.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(308): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(298): Show |
8 | a0001c0003t0001g0170a0001c0003t0001g0171a0001c0003t0001g0172others(5): Show | 8 | HG01081.hp2 HG01256.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(309): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(299): Show |
5 | a0001c0003t0001g0024a0001c0003t0001g0176a0001c0003t0001g0301others(2): Show | 5 | HG01258.hp2 HG02738.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(310): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(300): Show |
8 | a0001c0003t0001g0145a0001c0003t0001g0260a0001c0003t0001g0262others(5): Show | 8 | HG00738.hp2 HG01099.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(311): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(301): Show |
1 | a0001c0003t0001g0266 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(312): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(302): Show |
1 | a0001c0003t0001g0273 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(313): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(303): Show |
2 | a0001c0001t0002g0267a0001c0001t0003g0187 | 2 | HG01071.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(314): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(304): Show |
4 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0351others(1): Show | 4 | HG00639.hp2 HG02602.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(315): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(305): Show |
13 | a0001c0001t0002g0214a0001c0001t0002g0234a0001c0001t0002g0268others(10): Show | 13 | HG00408.hp1 HG01109.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(316): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(306): Show |
3 | a0001c0001t0002g0046a0001c0001t0002g0052a0001c0003t0001g0265 | 3 | HG00408.hp2 HG01175.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(317): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(308): Show |
3 | a0001c0001t0002g0233a0001c0003t0001g0060a0001c0003t0001g0079 | 3 | HG01243.hp1 HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(319): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(309): Show |
3 | a0001c0001t0002g0235a0001c0001t0002g0236a0004c0006t0001g0344 | 3 | HG01099.hp2 NA19057.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(320): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(310): Show |
3 | a0001c0001t0002g0237a0001c0003t0001g0021a0001c0003t0001g0031 | 3 | HG02056.hp2 HG02145.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(321): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(311): Show |
4 | a0001c0003t0001g0097a0001c0003t0001g0177a0001c0003t0001g0252others(1): Show | 4 | HG01978.hp2 HG02523.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(322): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(313): Show |
1 | a0001c0001t0002g0213 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(324): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781773
|
C | CAGATTTT others(315): Show |
1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(326): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | |||||
| chr6:109781800
|
C | T | 28 | a0002c0002t0002g0007a0002c0002t0003g0209a0002c0002t0004g0006others(25): Show | 28 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1890-3170C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781800 | ||||||
| chr6:109782055
|
C | T | 1 | a0001c0003t0001g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1890-2915C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782055 | ||||||
| chr6:109782078
|
T | G | 6 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0083others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1890-2892T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782078 | ||||||
| chr6:109782477
|
G | C | 1 | a0004c0006t0001g0307 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1890-2493G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782477 | ||||||
| chr6:109782565
|
C | T | 1 | a0002c0012t0001g0137 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1890-2405C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782565 | ||||||
| chr6:109782569
|
T | A | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1890-2401T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782569 | ||||||
| chr6:109782599
|
CT | C | 139 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(136): Show | 140 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1890-2368delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109782599 | |||||
| chr6:109782633
|
T | C | 30 | a0001c0001t0002g0104a0001c0001t0003g0001a0001c0001t0003g0022others(27): Show | 31 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(28): Show |
intron_variant | MODIFIER | c.1890-2337T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782633 | ||||||
| chr6:109782694
|
A | T | 1 | a0004c0006t0001g0307 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1890-2276A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782694 | ||||||
| chr6:109782884
|
A | C | 1 | a0001c0003t0001g0262 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1890-2086A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782884 | ||||||
| chr6:109782927
|
C | T | 103 | a0001c0001t0002g0046a0001c0001t0002g0052a0001c0001t0002g0213others(100): Show | 103 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1890-2043C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782927 | ||||||
| chr6:109782945
|
T | C | 1 | a0001c0001t0002g0019 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1890-2025T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782945 | ||||||
| chr6:109783006
|
T | C | 2 | a0002c0002t0002g0012a0002c0002t0002g0013 | 2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1890-1964T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783006 | ||||||
| chr6:109783095
|
A | C | 1 | a0002c0002t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1890-1875A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783095 | ||||||
| chr6:109783151
|
G | A | 3 | a0002c0002t0002g0005a0002c0002t0004g0294a0002c0002t0005g0125 | 3 | HG02451.hp2 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1890-1819G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783151 | ||||||
| chr6:109783243
|
G | A | 25 | a0002c0002t0002g0005a0002c0002t0002g0008a0002c0002t0002g0069others(22): Show | 25 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.1890-1727G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783243 | ||||||
| chr6:109783500
|
A | T | 29 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0023others(26): Show | 30 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(27): Show |
intron_variant | MODIFIER | c.1890-1470A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783500 | ||||||
| chr6:109783860
|
T | A | 1 | a0002c0002t0004g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1890-1110T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783860 | ||||||
| chr6:109783894
|
G | A | 29 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0023others(26): Show | 30 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(27): Show |
intron_variant | MODIFIER | c.1890-1076G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783894 | ||||||
| chr6:109784116
|
A | G | 1 | a0004c0006t0001g0324 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1890-854A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109784116 | ||||||
| chr6:109784260
|
G | T | 2 | a0002c0002t0002g0012a0002c0002t0002g0013 | 2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1890-710G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109784260 | ||||||
| chr6:109784266
|
A | G | 13 | a0002c0002t0004g0006a0002c0002t0004g0196a0002c0002t0004g0197others(10): Show | 13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1890-704A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109784266 | ||||||
| chr6:109784412
|
G | A | 1 | a0001c0003t0001g0024 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1890-558G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109784412 | ||||||
| chr6:109784551
|
G | A | 3 | a0003c0005t0001g0332a0003c0005t0001g0334a0003c0007t0001g0347 | 3 | NA18955.hp1 NA18967.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1890-419G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109784551 | ||||||
| chr6:109784869
|
G | T | 25 | a0002c0002t0002g0005a0002c0002t0002g0008a0002c0002t0002g0069others(22): Show | 25 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.1890-101G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109784869 | ||||||
| chr6:109785031
|
A | G | 112 | a0001c0001t0002g0046a0001c0001t0002g0052a0001c0001t0002g0124others(109): Show | 112 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
splice_region_variant&intron_variant | LOW | c.1948+3A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785031 | ||||||
| chr6:109785074
|
C | A | 131 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0133others(128): Show | 132 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1948+46C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785074 | ||||||
| chr6:109785084
|
T | C | 2 | a0002c0002t0005g0126a0002c0002t0005g0127 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1948+56T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785084 | ||||||
| chr6:109785119
|
T | G | 1 | a0001c0001t0002g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1948+91T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785119 | ||||||
| chr6:109785356
|
A | G | 1 | a0003c0005t0001g0349 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1948+328A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785356 | ||||||
| chr6:109785380
|
G | A | 43 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(40): Show | 44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.1948+352G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785380 | ||||||
| chr6:109785399
|
G | A | 19 | a0002c0002t0002g0008a0002c0002t0002g0110a0002c0002t0002g0111others(16): Show | 19 | HG02257.hp2 HG02615.hp1 HG02647.hp2 others(16): Show |
intron_variant | MODIFIER | c.1948+371G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785399 | ||||||
| chr6:109785498
|
A | G | 1 | a0001c0003t0001g0270 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1948+470A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785498 | ||||||
| chr6:109785538
|
A | T | 165 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0133others(162): Show | 166 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.1948+510A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785538 | ||||||
| chr6:109785692
|
C | T | 2 | a0002c0002t0002g0007a0002c0009t0002g0158 | 2 | HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1949-610C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785692 | ||||||
| chr6:109785707
|
C | T | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1949-595C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785707 | ||||||
| chr6:109785863
|
T | C | 1 | a0002c0002t0002g0069 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1949-439T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785863 | ||||||
| chr6:109785911
|
C | T | 3 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0262 | 3 | HG01099.hp1 HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1949-391C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785911 | ||||||
| chr6:109785994
|
G | A | 112 | a0001c0001t0002g0046a0001c0001t0002g0052a0001c0001t0002g0124others(109): Show | 112 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1949-308G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785994 | ||||||
| chr6:109786075
|
C | T | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1949-227C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109786075 | ||||||
| chr6:109786125
|
A | C | 15 | a0001c0001t0003g0001a0001c0001t0003g0162a0001c0001t0003g0163others(12): Show | 16 | HG00438.hp1 NA18939.hp1 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.1949-177A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109786125 | ||||||
| chr6:109786131
|
C | T | 1 | a0002c0004t0001g0051 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1949-171C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109786131 | ||||||
| chr6:109786154
|
A | G | 6 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0083others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1949-148A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109786154 | ||||||
| chr6:109786181
|
G | A | 2 | a0002c0002t0005g0126a0002c0002t0005g0127 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1949-121G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109786181 | ||||||
| chr6:109786860
|
G | C | 26 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(23): Show | 26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2096+411G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109786860 | ||||||
| chr6:109787146
|
C | T | 2 | a0002c0002t0004g0006a0002c0002t0004g0197 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2096+697C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787146 | ||||||
| chr6:109787236
|
A | G | 2 | a0001c0001t0002g0042a0001c0001t0002g0361 | 2 | HG00438.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.2096+787A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787236 | ||||||
| chr6:109787242
|
A | G | 26 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(23): Show | 26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2096+793A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787242 | ||||||
| chr6:109787299
|
T | C | 29 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0023others(26): Show | 30 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(27): Show |
intron_variant | MODIFIER | c.2096+850T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787299 | ||||||
| chr6:109787359
|
C | T | 29 | a0002c0004t0001g0028a0002c0004t0001g0037a0002c0004t0001g0039others(26): Show | 29 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.2096+910C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787359 | ||||||
| chr6:109787421
|
T | C | 2 | a0002c0002t0005g0126a0002c0002t0005g0127 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2096+972T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787421 | ||||||
| chr6:109787423
|
G | T | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2096+974G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787423 | ||||||
| chr6:109787652
|
G | T | 306 | a0001c0001t0002g0046a0001c0001t0002g0052a0001c0001t0002g0124others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.2096+1203G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787652 | ||||||
| chr6:109787884
|
C | A | 1 | a0001c0001t0002g0299 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2096+1435C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787884 | ||||||
| chr6:109787962
|
A | G | 1 | a0002c0004t0001g0129 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2096+1513A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787962 | ||||||
| chr6:109788239
|
A | G | 1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2097-1355A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109788239 | ||||||
| chr6:109788371
|
G | A | 1 | a0002c0002t0004g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2097-1223G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109788371 | ||||||
| chr6:109788576
|
G | A | 22 | a0002c0002t0002g0005a0002c0002t0002g0008a0002c0002t0002g0110others(19): Show | 22 | HG02257.hp2 HG02451.hp2 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.2097-1018G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109788576 | ||||||
| chr6:109788588
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2097-1006C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109788588 | ||||||
| chr6:109788664
|
C | T | 3 | a0002c0002t0004g0355a0002c0002t0004g0356a0002c0002t0004g0357 | 3 | HG01081.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2097-930C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109788664 | ||||||
| chr6:109788673
|
G | A | 2 | a0002c0002t0004g0294a0002c0002t0005g0125 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2097-921G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109788673 | ||||||
| chr6:109789007
|
T | C | 1 | a0001c0001t0003g0022 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2097-587T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789007 | ||||||
| chr6:109789036
|
G | A | 4 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0099others(1): Show | 4 | HG00423.hp1 HG00544.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.2097-558G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789036 | ||||||
| chr6:109789099
|
A | G | 15 | a0001c0001t0003g0001a0001c0001t0003g0162a0001c0001t0003g0163others(12): Show | 16 | HG00438.hp1 NA18939.hp1 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.2097-495A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789099 | ||||||
| chr6:109789126
|
T | C | 2 | a0002c0002t0002g0069a0002c0002t0002g0211 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2097-468T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789126 | ||||||
| chr6:109789222
|
C | A | 1 | a0002c0002t0001g0146 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2097-372C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789222 | ||||||
| chr6:109789351
|
A | C | 307 | a0001c0001t0002g0046a0001c0001t0002g0052a0001c0001t0002g0104others(304): Show | 309 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(306): Show |
intron_variant | MODIFIER | c.2097-243A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789351 | ||||||
| chr6:109789377
|
C | T | 29 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0023others(26): Show | 30 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(27): Show |
intron_variant | MODIFIER | c.2097-217C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789377 | ||||||
| chr6:109789740
|
G | T | 104 | a0001c0001t0002g0046a0001c0001t0002g0052a0001c0001t0002g0213others(101): Show | 104 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2180+63G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109789740 | ||||||
| chr6:109789858
|
T | C | 2 | a0001c0001t0003g0365a0001c0001t0003g0366 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2180+181T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109789858 | ||||||
| chr6:109790073
|
T | A | 103 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0133others(100): Show | 104 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.2180+396T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109790073 | ||||||
| chr6:109790810
|
T | TC | 60 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0133others(57): Show | 60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.2181-560dupC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 109790810 | |||||
| chr6:109790814
|
C | T | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2181-562C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109790814 | ||||||
| chr6:109790821
|
A | G | 5 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(2): Show | 5 | HG02615.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2181-555A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109790821 | ||||||
| chr6:109790831
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2181-545A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109790831 | ||||||
| chr6:109790912
|
T | G | 8 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(5): Show | 8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2181-464T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109790912 | ||||||
| chr6:109790973
|
G | A | 14 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0196others(11): Show | 14 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2181-403G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109790973 | ||||||
| chr6:109791009
|
T | A | 43 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(40): Show | 44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2181-367T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109791009 | ||||||
| chr6:109791012
|
C | T | 43 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(40): Show | 44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2181-364C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109791012 | ||||||
| chr6:109791126
|
T | A | 1 | a0001c0001t0003g0023 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2181-250T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109791126 | ||||||
| chr6:109791133
|
C | T | 3 | a0001c0003t0001g0166a0001c0003t0001g0173a0001c0003t0001g0177 | 3 | HG00741.hp1 HG01978.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2181-243C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109791133 | ||||||
| chr6:109791731
|
A | C | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2376+160A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | chr6 | 109791731 | ||||||
| chr6:109791900
|
G | A | 1 | a0002c0009t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2376+329G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | chr6 | 109791900 | ||||||
| chr6:109792008
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2376+437C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | chr6 | 109792008 | ||||||
| chr6:109792166
|
A | C | 1 | a0003c0005t0001g0325 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2377-416A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | chr6 | 109792166 | ||||||
| chr6:109792560
|
CT | C | 44 | a0001c0001t0002g0267a0001c0001t0002g0268a0002c0004t0001g0128others(41): Show | 45 | HG00639.hp1 HG01071.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.2377-10delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr6 | 109792560 | |||||
| chr6:109792562
|
T | TC | 22 | a0002c0004t0001g0028a0002c0004t0001g0037a0002c0004t0001g0039others(19): Show | 22 | HG00099.hp1 HG00423.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.2377-20_2377-19ins others(1): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | chr6 | 109792562 | ||||||
| chr6:109792563
|
T | C | 36 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0133others(33): Show | 36 | HG00323.hp2 HG00544.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.2377-19T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | chr6 | 109792563 | ||||||
| chr6:109792723
|
C | T | 2 | a0002c0002t0004g0294a0002c0002t0005g0125 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2459+59C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109792723 | ||||||
| chr6:109792736
|
C | CT | 15 | a0001c0001t0002g0104a0002c0004t0001g0028a0002c0004t0001g0039others(12): Show | 15 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2459+91dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109792736 | |||||
| chr6:109792736
|
CT | C | 193 | a0001c0001t0002g0046a0001c0001t0002g0052a0001c0001t0002g0056others(190): Show | 194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.2459+91delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109792736 | |||||
| chr6:109792736
|
CTT | C | 40 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0227others(37): Show | 40 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.2459+90_2459+91del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109792736 | |||||
| chr6:109792814
|
C | T | 1 | a0002c0002t0002g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2459+150C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109792814 | ||||||
| chr6:109792858
|
T | C | 3 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0014t0002g0011 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2459+194T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109792858 | ||||||
| chr6:109793118
|
A | AAATG | 4 | a0001c0003t0001g0254a0001c0003t0001g0291a0001c0003t0001g0292others(1): Show | 4 | NA18949.hp2 NA18974.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.2459+455_2459+458d others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109793118 | |||||
| chr6:109793277
|
A | G | 1 | a0001c0003t0001g0079 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2459+613A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793277 | ||||||
| chr6:109793296
|
C | T | 1 | a0002c0002t0005g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2459+632C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793296 | ||||||
| chr6:109793400
|
T | G | 6 | a0002c0002t0002g0010a0002c0002t0002g0083a0002c0002t0002g0084others(3): Show | 6 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2459+736T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793400 | ||||||
| chr6:109793457
|
C | T | 22 | a0002c0002t0002g0005a0002c0002t0002g0008a0002c0002t0002g0110others(19): Show | 22 | HG02257.hp2 HG02451.hp2 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.2459+793C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793457 | ||||||
| chr6:109793465
|
T | C | 2 | a0001c0001t0002g0224a0006c0013t0002g0222 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2459+801T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793465 | ||||||
| chr6:109793473
|
C | G | 37 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(34): Show | 38 | HG00438.hp1 HG00558.hp2 HG02109.hp2 others(35): Show |
intron_variant | MODIFIER | c.2459+809C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793473 | ||||||
| chr6:109793518
|
T | C | 15 | a0002c0002t0002g0008a0002c0002t0002g0110a0002c0002t0002g0111others(12): Show | 15 | HG02257.hp2 HG02615.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.2459+854T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793518 | ||||||
| chr6:109793625
|
A | T | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2459+961A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793625 | ||||||
| chr6:109793669
|
T | C | 1 | a0002c0002t0002g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2459+1005T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793669 | ||||||
| chr6:109793702
|
G | C | 30 | a0001c0001t0002g0279a0002c0002t0002g0005a0002c0002t0002g0008others(27): Show | 30 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(27): Show |
intron_variant | MODIFIER | c.2459+1038G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793702 | ||||||
| chr6:109793703
|
C | T | 30 | a0002c0002t0002g0010a0002c0002t0002g0083a0002c0002t0002g0084others(27): Show | 30 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.2459+1039C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793703 | ||||||
| chr6:109793933
|
A | G | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2459+1269A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793933 | ||||||
| chr6:109793963
|
T | C | 27 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(24): Show | 27 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2459+1299T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793963 | ||||||
| chr6:109794273
|
C | T | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2459+1609C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109794273 | ||||||
| chr6:109794396
|
G | C | 1 | a0001c0001t0002g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2459+1732G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109794396 | ||||||
| chr6:109794732
|
C | T | 23 | a0002c0002t0002g0005a0002c0002t0002g0008a0002c0002t0002g0086others(20): Show | 23 | HG02257.hp2 HG02451.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.2460-2033C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109794732 | ||||||
| chr6:109794986
|
C | T | 3 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0014t0002g0011 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2460-1779C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109794986 | ||||||
| chr6:109794988
|
C | T | 1 | a0002c0004t0001g0040 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2460-1777C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109794988 | ||||||
| chr6:109795038
|
A | G | 3 | a0002c0002t0002g0069a0002c0002t0002g0211a0002c0004t0001g0160 | 3 | HG02109.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2460-1727A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795038 | ||||||
| chr6:109795094
|
AGTTTTTT others(5): Show |
A | 7 | a0001c0001t0003g0163a0001c0001t0003g0182a0001c0001t0003g0184others(4): Show | 7 | HG02818.hp1 NA18952.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.2460-1670_2460-165 others(16): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795094 | ||||||
| chr6:109795094
|
AGTTTTTT others(6): Show |
A | 30 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(27): Show | 31 | HG00438.hp1 HG00558.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2460-1670_2460-165 others(17): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795094 | ||||||
| chr6:109795095
|
G | GT | 8 | a0001c0001t0002g0015a0001c0001t0002g0042a0001c0001t0002g0055others(5): Show | 8 | HG00438.hp2 HG00738.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.2460-1630dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
G | GTTT | 7 | a0001c0001t0002g0018a0001c0001t0002g0030a0001c0001t0002g0098others(4): Show | 7 | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.2460-1632_2460-163 others(7): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0002g0048a0001c0001t0002g0049 | 2 | HG00558.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.2460-1639_2460-163 others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
G | GTTTTTTT others(4): Show |
2 | a0001c0001t0002g0227a0001c0001t0002g0241 | 2 | HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2460-1640_2460-163 others(15): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
G | GTTTTTTT others(6): Show |
1 | a0001c0001t0002g0038 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2460-1642_2460-163 others(17): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
GT | G | 21 | a0001c0001t0002g0017a0001c0001t0002g0019a0001c0001t0002g0025others(18): Show | 21 | HG02004.hp1 HG02280.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.2460-1630delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
GTTTTTTT others(3): Show |
G | 1 | a0002c0002t0002g0069 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2460-1639_2460-163 others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
GTTTTTTT others(4): Show |
G | 6 | a0002c0002t0002g0116a0002c0002t0002g0118a0002c0002t0002g0121others(3): Show | 6 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2460-1640_2460-163 others(15): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
GTTTTTTT others(5): Show |
G | 24 | a0002c0002t0001g0143a0002c0002t0001g0149a0002c0002t0001g0154others(21): Show | 24 | HG01261.hp1 HG02135.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.2460-1641_2460-163 others(16): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
GTTTTTTT others(6): Show |
G | 66 | a0001c0003t0001g0034a0001c0003t0001g0060a0001c0003t0001g0073others(63): Show | 66 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.2460-1642_2460-163 others(17): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
GTTTTTTT others(7): Show |
G | 71 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0014others(68): Show | 71 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.2460-1643_2460-163 others(18): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
GTTTTTTT others(8): Show |
G | 27 | a0001c0003t0001g0259a0001c0003t0001g0285a0002c0002t0003g0209others(24): Show | 27 | HG01069.hp2 HG01081.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.2460-1644_2460-163 others(19): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0002g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2460-1645_2460-163 others(20): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
GTTTTTTT others(10): Show |
G | 2 | a0001c0001t0002g0267a0001c0001t0002g0268 | 2 | HG01071.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2460-1646_2460-163 others(21): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
GTTTTTTT others(13): Show |
G | 2 | a0002c0002t0002g0084a0002c0002t0002g0085 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2460-1649_2460-163 others(24): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795095
|
GTTTTTTT others(15): Show |
G | 1 | a0001c0001t0002g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2460-1651_2460-163 others(26): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | |||||
| chr6:109795105
|
T | TTG | 12 | a0002c0004t0001g0174a0002c0004t0001g0178a0003c0005t0001g0312others(9): Show | 12 | HG00639.hp1 HG01175.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.2460-1659_2460-165 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795105 | |||||
| chr6:109795106
|
T | TG | 29 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0189others(26): Show | 30 | HG01255.hp2 HG01358.hp2 HG01934.hp2 others(27): Show |
intron_variant | MODIFIER | c.2460-1659_2460-165 others(5): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795106 | ||||||
| chr6:109795113
|
T | G | 1 | a0002c0014t0002g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2460-1652T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795113 | ||||||
| chr6:109795118
|
T | G | 2 | a0002c0009t0002g0157a0002c0009t0002g0159 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2460-1647T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795118 | ||||||
| chr6:109795122
|
T | G | 1 | a0003c0005t0001g0340 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2460-1643T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795122 | ||||||
| chr6:109795139
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2460-1626A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795139 | ||||||
| chr6:109795162
|
G | A | 1 | a0002c0004t0001g0037 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2460-1603G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795162 | ||||||
| chr6:109795225
|
C | T | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2460-1540C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795225 | ||||||
| chr6:109795403
|
T | A | 29 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0133others(26): Show | 29 | HG00323.hp2 HG00544.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.2460-1362T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795403 | ||||||
| chr6:109795558
|
AAAGGAAA others(1): Show |
A | 27 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(24): Show | 27 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2460-1198_2460-119 others(12): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795558 | |||||
| chr6:109795595
|
C | CT | 15 | a0002c0002t0001g0134a0002c0002t0002g0009a0002c0002t0002g0010others(12): Show | 15 | HG01261.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2460-1144dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | |||||
| chr6:109795595
|
C | CTT | 86 | a0001c0001t0002g0017a0001c0001t0002g0057a0001c0001t0002g0091others(83): Show | 86 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.2460-1145_2460-114 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | |||||
| chr6:109795595
|
C | CTTT | 96 | a0001c0001t0002g0015a0001c0001t0002g0018a0001c0001t0002g0019others(93): Show | 96 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.2460-1146_2460-114 others(7): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | |||||
| chr6:109795595
|
C | CTTTT | 79 | a0001c0001t0002g0030a0001c0001t0002g0046a0001c0001t0002g0048others(76): Show | 79 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.2460-1147_2460-114 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | |||||
| chr6:109795595
|
C | CTTTTT | 12 | a0001c0001t0002g0107a0001c0003t0001g0033a0001c0003t0001g0060others(9): Show | 12 | HG00735.hp2 HG02015.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.2460-1148_2460-114 others(9): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | |||||
| chr6:109795595
|
CTTTT | C | 12 | a0001c0001t0003g0001a0001c0001t0003g0163a0001c0001t0003g0168others(9): Show | 13 | HG00438.hp1 NA18939.hp1 NA18940.hp1 others(10): Show |
intron_variant | MODIFIER | c.2460-1147_2460-114 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | |||||
| chr6:109795595
|
CTTTTTTT others(4): Show |
C | 40 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(37): Show | 41 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.2460-1154_2460-114 others(15): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | |||||
| chr6:109795663
|
A | G | 166 | a0001c0001t0002g0279a0002c0002t0001g0130a0002c0002t0001g0132others(163): Show | 167 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.2460-1102A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795663 | ||||||
| chr6:109795769
|
T | A | 27 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(24): Show | 27 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2460-996T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795769 | ||||||
| chr6:109795803
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2460-962G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795803 | ||||||
| chr6:109795823
|
G | A | 3 | a0002c0002t0002g0005a0002c0002t0004g0294a0002c0002t0005g0125 | 3 | HG02451.hp2 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2460-942G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795823 | ||||||
| chr6:109795892
|
C | T | 3 | a0002c0002t0002g0007a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG02809.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2460-873C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795892 | ||||||
| chr6:109795893
|
G | A | 1 | a0002c0002t0004g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2460-872G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795893 | ||||||
| chr6:109795895
|
G | A | 23 | a0002c0002t0002g0005a0002c0002t0002g0008a0002c0002t0002g0086others(20): Show | 23 | HG02257.hp2 HG02451.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.2460-870G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795895 | ||||||
| chr6:109795919
|
A | T | 27 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(24): Show | 27 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2460-846A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795919 | ||||||
| chr6:109795967
|
C | T | 80 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0014others(77): Show | 80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.2460-798C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795967 | ||||||
| chr6:109796237
|
G | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0017 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2460-528G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109796237 | ||||||
| chr6:109796513
|
A | G | 29 | a0002c0004t0001g0028a0002c0004t0001g0037a0002c0004t0001g0039others(26): Show | 29 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.2460-252A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109796513 | ||||||
| chr6:109796546
|
A | G | 1 | a0001c0001t0003g0187 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2460-219A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109796546 | ||||||
| chr6:109796559
|
A | G | 1 | a0002c0002t0002g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2460-206A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109796559 | ||||||
| chr6:109796638
|
C | T | 26 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(23): Show | 26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2460-127C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109796638 | ||||||
| chr6:109796727
|
C | T | 3 | a0002c0002t0002g0007a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG02809.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2460-38C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109796727 | ||||||
| chr6:109797009
|
C | T | 30 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0023others(27): Show | 31 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(28): Show |
intron_variant | MODIFIER | c.2546+158C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797009 | ||||||
| chr6:109797236
|
T | G | 43 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(40): Show | 44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2546+385T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797236 | ||||||
| chr6:109797282
|
C | T | 1 | a0007c0016t0001g0078 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2546+431C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797282 | ||||||
| chr6:109797383
|
A | G | 285 | a0001c0001t0002g0104a0001c0001t0002g0124a0001c0001t0002g0221others(282): Show | 287 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.2546+532A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797383 | ||||||
| chr6:109797472
|
T | C | 2 | a0003c0007t0001g0321a0003c0018t0001g0318 | 2 | NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2546+621T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797472 | ||||||
| chr6:109797571
|
C | G | 1 | a0005c0019t0006g0016 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2546+720C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797571 | ||||||
| chr6:109797573
|
G | A | 285 | a0001c0001t0002g0104a0001c0001t0002g0124a0001c0001t0002g0221others(282): Show | 287 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.2546+722G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797573 | ||||||
| chr6:109797896
|
C | CA | 11 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0048others(8): Show | 11 | HG01928.hp2 HG02074.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.2546+1064dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109797896 | |||||
| chr6:109797896
|
CA | C | 105 | a0001c0001t0002g0081a0001c0001t0002g0224a0001c0003t0001g0165others(102): Show | 106 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.2546+1064delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109797896 | |||||
| chr6:109797915
|
A | AG | 3 | a0002c0002t0003g0209a0002c0002t0004g0123a0002c0002t0004g0229 | 3 | HG02258.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2546+1064_2546+106 others(5): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797915 | ||||||
| chr6:109797915
|
A | G | 23 | a0002c0002t0004g0006a0002c0002t0004g0186a0002c0002t0004g0196others(20): Show | 23 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2546+1064A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797915 | ||||||
| chr6:109798008
|
G | A | 1 | a0002c0004t0001g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2546+1157G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798008 | ||||||
| chr6:109798395
|
T | C | 1 | a0001c0003t0001g0262 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2546+1544T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798395 | ||||||
| chr6:109798541
|
T | A | 1 | a0001c0003t0001g0252 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2546+1690T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798541 | ||||||
| chr6:109798611
|
G | A | 3 | a0002c0002t0002g0007a0002c0002t0005g0126a0002c0002t0005g0127 | 3 | HG02809.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2546+1760G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798611 | ||||||
| chr6:109798816
|
CT | C | 16 | a0001c0003t0001g0145a0002c0002t0003g0209a0002c0002t0004g0006others(13): Show | 16 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2546+1975delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109798816 | |||||
| chr6:109798831
|
G | A | 40 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(37): Show | 41 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.2546+1980G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798831 | ||||||
| chr6:109798842
|
C | A | 3 | a0001c0003t0001g0024a0001c0003t0001g0300a0001c0003t0001g0301 | 3 | HG01256.hp1 HG01258.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2546+1991C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798842 | ||||||
| chr6:109798889
|
A | G | 1 | a0003c0005t0001g0250 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2546+2038A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798889 | ||||||
| chr6:109798924
|
T | G | 1 | a0001c0001t0002g0052 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2546+2073T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798924 | ||||||
| chr6:109798928
|
T | G | 285 | a0001c0001t0002g0104a0001c0001t0002g0124a0001c0001t0002g0221others(282): Show | 287 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.2546+2077T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798928 | ||||||
| chr6:109799064
|
A | C | 58 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0133others(55): Show | 58 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.2546+2213A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109799064 | ||||||
| chr6:109799088
|
C | T | 2 | a0001c0003t0001g0285a0001c0003t0001g0286 | 2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2546+2237C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109799088 | ||||||
| chr6:109799321
|
A | G | 285 | a0001c0001t0002g0104a0001c0001t0002g0124a0001c0001t0002g0221others(282): Show | 287 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.2546+2470A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109799321 | ||||||
| chr6:109799363
|
GGT | G | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0083others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2546+2524_2546+252 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109799363 | |||||
| chr6:109799409
|
T | C | 2 | a0002c0002t0002g0084a0002c0002t0002g0085 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2546+2558T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109799409 | ||||||
| chr6:109799427
|
C | T | 43 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(40): Show | 44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2546+2576C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109799427 | ||||||
| chr6:109799442
|
A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2546+2591A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109799442 | ||||||
| chr6:109800028
|
A | G | 1 | a0002c0004t0004g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2546+3177A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800028 | ||||||
| chr6:109800161
|
A | G | 3 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0014t0002g0011 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2546+3310A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800161 | ||||||
| chr6:109800247
|
T | G | 367 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(364): Show | 369 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.2546+3396T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800247 | ||||||
| chr6:109800248
|
T | G | 367 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0018others(364): Show | 369 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.2546+3397T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800248 | ||||||
| chr6:109800429
|
T | G | 1 | a0001c0003t0001g0297 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2546+3578T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800429 | ||||||
| chr6:109800552
|
A | C | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+3701A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800552 | ||||||
| chr6:109800567
|
G | A | 1 | a0002c0002t0002g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2546+3716G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800567 | ||||||
| chr6:109800635
|
ACT | A | 21 | a0001c0003t0001g0014a0001c0003t0001g0021a0001c0003t0001g0031others(18): Show | 21 | HG00408.hp1 HG00741.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.2546+3785_2546+378 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800635 | ||||||
| chr6:109800671
|
G | A | 1 | a0002c0004t0001g0064 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2546+3820G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800671 | ||||||
| chr6:109800806
|
C | T | 256 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.2546+3955C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800806 | ||||||
| chr6:109801007
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2546+4156A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801007 | ||||||
| chr6:109801055
|
A | C | 1 | a0002c0002t0003g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2546+4204A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801055 | ||||||
| chr6:109801098
|
T | C | 1 | a0001c0003t0001g0031 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2546+4247T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801098 | ||||||
| chr6:109801147
|
A | G | 2 | a0002c0009t0002g0157a0002c0009t0002g0159 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2546+4296A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801147 | ||||||
| chr6:109801178
|
T | C | 1 | a0001c0001t0002g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2546+4327T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801178 | ||||||
| chr6:109801316
|
G | A | 1 | a0001c0003t0001g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2546+4465G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801316 | ||||||
| chr6:109801420
|
C | T | 1 | a0002c0004t0001g0215 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2546+4569C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801420 | ||||||
| chr6:109801425
|
A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2546+4574A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801425 | ||||||
| chr6:109801437
|
A | G | 1 | a0003c0005t0001g0249 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2546+4586A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801437 | ||||||
| chr6:109801455
|
G | A | 1 | a0001c0003t0001g0033 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2546+4604G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801455 | ||||||
| chr6:109801534
|
C | T | 1 | a0002c0002t0005g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2546+4683C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801534 | ||||||
| chr6:109801591
|
A | G | 4 | a0002c0002t0004g0228a0002c0002t0004g0229a0002c0002t0004g0238others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2546+4740A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801591 | ||||||
| chr6:109801599
|
A | G | 1 | a0001c0003t0001g0036 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2546+4748A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801599 | ||||||
| chr6:109801649
|
G | A | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0083others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2546+4798G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801649 | ||||||
| chr6:109801661
|
C | T | 2 | a0002c0002t0002g0012a0002c0002t0002g0013 | 2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2546+4810C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801661 | ||||||
| chr6:109801760
|
A | G | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+4909A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801760 | ||||||
| chr6:109801882
|
A | T | 1 | a0001c0001t0002g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2546+5031A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801882 | ||||||
| chr6:109802115
|
G | A | 283 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(282): Show |
intron_variant | MODIFIER | c.2546+5264G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109802115 | ||||||
| chr6:109802246
|
A | T | 1 | a0002c0004t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2546+5395A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109802246 | ||||||
| chr6:109802276
|
C | T | 1 | a0003c0005t0001g0325 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2546+5425C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109802276 | ||||||
| chr6:109802485
|
C | T | 29 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0133others(26): Show | 29 | HG00323.hp2 HG00544.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.2546+5634C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109802485 | ||||||
| chr6:109802702
|
T | C | 1 | a0001c0003t0001g0044 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2546+5851T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109802702 | ||||||
| chr6:109802731
|
A | C | 43 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(40): Show | 44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2546+5880A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109802731 | ||||||
| chr6:109803158
|
T | G | 26 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(23): Show | 26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2546+6307T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803158 | ||||||
| chr6:109803223
|
G | A | 23 | a0002c0002t0002g0005a0002c0002t0002g0008a0002c0002t0002g0086others(20): Show | 23 | HG02257.hp2 HG02451.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.2546+6372G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803223 | ||||||
| chr6:109803303
|
G | T | 1 | a0002c0002t0004g0360 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2546+6452G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803303 | ||||||
| chr6:109803317
|
G | A | 6 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(3): Show | 6 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2546+6466G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803317 | ||||||
| chr6:109803325
|
C | G | 87 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(84): Show | 87 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2546+6474C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803325 | ||||||
| chr6:109803330
|
A | G | 7 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(4): Show | 7 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2546+6479A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803330 | ||||||
| chr6:109803528
|
C | A | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2546+6677C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803528 | ||||||
| chr6:109803621
|
C | CT | 37 | a0001c0001t0002g0048a0001c0003t0001g0003a0001c0003t0001g0004others(34): Show | 37 | HG00408.hp1 HG00741.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.2546+6780dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109803621 | |||||
| chr6:109803621
|
CT | C | 59 | a0001c0001t0002g0124a0002c0002t0001g0130a0002c0002t0001g0132others(56): Show | 59 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.2546+6780delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109803621 | |||||
| chr6:109803768
|
C | A | 2 | a0002c0002t0002g0012a0002c0002t0002g0013 | 2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2546+6917C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803768 | ||||||
| chr6:109803775
|
C | G | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2546+6924C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803775 | ||||||
| chr6:109803808
|
C | G | 2 | a0002c0002t0002g0069a0002c0002t0002g0211 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2546+6957C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803808 | ||||||
| chr6:109803989
|
A | C | 43 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(40): Show | 44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2546+7138A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803989 | ||||||
| chr6:109804039
|
G | A | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2546+7188G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109804039 | ||||||
| chr6:109804162
|
A | G | 1 | a0005c0019t0006g0016 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2546+7311A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109804162 | ||||||
| chr6:109804246
|
C | T | 1 | a0001c0001t0003g0244 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2546+7395C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109804246 | ||||||
| chr6:109804392
|
T | A | 3 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0014t0002g0011 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2546+7541T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109804392 | ||||||
| chr6:109804431
|
T | A | 29 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0133others(26): Show | 29 | HG00323.hp2 HG00544.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.2546+7580T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109804431 | ||||||
| chr6:109805190
|
G | A | 2 | a0001c0003t0001g0285a0001c0003t0001g0286 | 2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2546+8339G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109805190 | ||||||
| chr6:109805201
|
A | G | 1 | a0001c0001t0003g0366 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2546+8350A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109805201 | ||||||
| chr6:109805230
|
C | T | 3 | a0002c0002t0004g0355a0002c0002t0004g0356a0002c0002t0004g0357 | 3 | HG01081.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2546+8379C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109805230 | ||||||
| chr6:109805591
|
A | G | 1 | a0002c0009t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2546+8740A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109805591 | ||||||
| chr6:109805628
|
A | G | 27 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(24): Show | 27 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2546+8777A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109805628 | ||||||
| chr6:109805728
|
TA | T | 4 | a0001c0001t0003g0023a0001c0001t0003g0187a0001c0001t0003g0194others(1): Show | 4 | NA18990.hp1 NA19009.hp2 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.2546+8879delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109805728 | |||||
| chr6:109806215
|
G | T | 2 | a0001c0003t0001g0319a0001c0003t0001g0368 | 2 | NA18969.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2546+9364G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806215 | ||||||
| chr6:109806286
|
C | G | 1 | a0003c0005t0001g0325 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2546+9435C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806286 | ||||||
| chr6:109806469
|
G | A | 1 | a0002c0002t0002g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2546+9618G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806469 | ||||||
| chr6:109806482
|
A | AGT | 3 | a0002c0002t0001g0135a0002c0002t0001g0218a0002c0002t0002g0116 | 3 | HG02886.hp1 NA18612.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2546+9645_2546+964 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109806482 | |||||
| chr6:109806516
|
A | G | 2 | a0001c0001t0002g0104a0001c0001t0003g0192 | 2 | NA18977.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2546+9665A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806516 | ||||||
| chr6:109806599
|
G | A | 1 | a0002c0002t0002g0363 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2546+9748G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806599 | ||||||
| chr6:109806666
|
A | G | 1 | a0001c0001t0003g0185 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2546+9815A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806666 | ||||||
| chr6:109806754
|
C | G | 88 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(85): Show | 88 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2546+9903C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806754 | ||||||
| chr6:109806787
|
G | C | 27 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(24): Show | 27 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2546+9936G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806787 | ||||||
| chr6:109807126
|
A | G | 3 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0014t0002g0011 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2546+10275A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807126 | ||||||
| chr6:109807226
|
A | G | 1 | a0002c0009t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2546+10375A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807226 | ||||||
| chr6:109807278
|
C | T | 30 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0023others(27): Show | 31 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(28): Show |
intron_variant | MODIFIER | c.2546+10427C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807278 | ||||||
| chr6:109807293
|
A | G | 1 | a0002c0002t0004g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2546+10442A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807293 | ||||||
| chr6:109807329
|
G | T | 1 | a0004c0006t0001g0307 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2546+10478G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807329 | ||||||
| chr6:109807395
|
C | T | 15 | a0002c0002t0002g0008a0002c0002t0002g0110a0002c0002t0002g0111others(12): Show | 15 | HG02257.hp2 HG02615.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.2546+10544C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807395 | ||||||
| chr6:109807425
|
G | A | 1 | a0001c0003t0001g0021 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2546+10574G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807425 | ||||||
| chr6:109807483
|
G | A | 79 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0014others(76): Show | 79 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.2546+10632G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807483 | ||||||
| chr6:109807528
|
T | C | 43 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(40): Show | 44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2546+10677T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807528 | ||||||
| chr6:109807546
|
A | C | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+10695A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807546 | ||||||
| chr6:109807560
|
C | G | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+10709C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807560 | ||||||
| chr6:109807882
|
T | C | 1 | a0001c0001t0002g0038 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2546+11031T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807882 | ||||||
| chr6:109808024
|
A | G | 1 | a0001c0001t0003g0193 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2546+11173A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808024 | ||||||
| chr6:109808130
|
A | G | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2546+11279A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808130 | ||||||
| chr6:109808310
|
A | G | 1 | a0002c0002t0002g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2546+11459A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808310 | ||||||
| chr6:109808350
|
C | CA | 59 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2546+11523dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109808350 | |||||
| chr6:109808350
|
C | CAA | 7 | a0001c0001t0002g0107a0002c0002t0001g0138a0002c0002t0001g0218others(4): Show | 7 | HG02056.hp1 HG02572.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.2546+11522_2546+11 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109808350 | |||||
| chr6:109808350
|
C | CAAA | 21 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0133others(18): Show | 21 | HG00323.hp2 HG00544.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.2546+11521_2546+11 others(9): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109808350 | |||||
| chr6:109808350
|
CA | C | 71 | a0001c0001t0002g0050a0001c0001t0002g0080a0001c0001t0002g0299others(68): Show | 72 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.2546+11523delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109808350 | |||||
| chr6:109808350
|
CAA | C | 80 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(77): Show | 80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.2546+11522_2546+11 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109808350 | |||||
| chr6:109808374
|
AG | A | 3 | a0002c0002t0001g0143a0002c0002t0001g0144a0002c0002t0001g0148 | 3 | NA18955.hp2 NA18998.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2546+11524delG | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808374 | ||||||
| chr6:109808375
|
G | A | 26 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0133others(23): Show | 26 | HG00323.hp2 HG00544.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.2546+11524G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808375 | ||||||
| chr6:109808544
|
G | A | 16 | a0002c0002t0001g0130a0002c0002t0001g0138a0002c0002t0001g0141others(13): Show | 16 | HG01943.hp1 HG01975.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.2546+11693G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808544 | ||||||
| chr6:109808763
|
T | A | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+11912T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808763 | ||||||
| chr6:109808961
|
A | G | 3 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0014t0002g0011 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2546+12110A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808961 | ||||||
| chr6:109809085
|
T | C | 70 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(67): Show | 71 | HG00639.hp1 HG01081.hp1 HG01175.hp2 others(68): Show |
intron_variant | MODIFIER | c.2546+12234T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109809085 | ||||||
| chr6:109809234
|
C | T | 3 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0014t0002g0011 | 3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2546+12383C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109809234 | ||||||
| chr6:109809328
|
T | C | 43 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(40): Show | 44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2546+12477T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109809328 | ||||||
| chr6:109809898
|
G | A | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+13047G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109809898 | ||||||
| chr6:109809938
|
C | G | 70 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(67): Show | 71 | HG00639.hp1 HG01081.hp1 HG01175.hp2 others(68): Show |
intron_variant | MODIFIER | c.2546+13087C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109809938 | ||||||
| chr6:109810049
|
C | T | 87 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(84): Show | 87 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2546+13198C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810049 | ||||||
| chr6:109810143
|
G | C | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2546+13292G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810143 | ||||||
| chr6:109810147
|
G | A | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+13296G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810147 | ||||||
| chr6:109810272
|
G | A | 1 | a0001c0001t0002g0268 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2546+13421G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810272 | ||||||
| chr6:109810389
|
T | C | 2 | a0001c0003t0001g0319a0001c0003t0001g0368 | 2 | NA18969.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2546+13538T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810389 | ||||||
| chr6:109810469
|
G | A | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+13618G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810469 | ||||||
| chr6:109810592
|
C | G | 10 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(7): Show | 10 | HG02257.hp2 HG02615.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2546+13741C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810592 | ||||||
| chr6:109810785
|
G | A | 70 | a0002c0002t0003g0209a0002c0002t0004g0006a0002c0002t0004g0123others(67): Show | 71 | HG00639.hp1 HG01081.hp1 HG01175.hp2 others(68): Show |
intron_variant | MODIFIER | c.2546+13934G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810785 | ||||||
| chr6:109810803
|
G | A | 44 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(41): Show | 45 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(42): Show |
intron_variant | MODIFIER | c.2546+13952G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810803 | ||||||
| chr6:109810821
|
T | G | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0083others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2546+13970T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810821 | ||||||
| chr6:109810898
|
G | C | 1 | a0002c0002t0002g0069 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2546+14047G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810898 | ||||||
| chr6:109811070
|
T | C | 1 | a0002c0002t0004g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2547-14018T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811070 | ||||||
| chr6:109811074
|
G | T | 1 | a0002c0009t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2547-14014G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811074 | ||||||
| chr6:109811106
|
A | G | 2 | a0002c0009t0002g0157a0002c0009t0002g0159 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2547-13982A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811106 | ||||||
| chr6:109811154
|
C | G | 1 | a0001c0001t0003g0022 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2547-13934C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811154 | ||||||
| chr6:109811174
|
G | A | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2547-13914G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811174 | ||||||
| chr6:109811347
|
G | A | 1 | a0002c0009t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2547-13741G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811347 | ||||||
| chr6:109811396
|
A | G | 45 | a0002c0002t0002g0211a0002c0002t0004g0305a0002c0004t0001g0128others(42): Show | 46 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.2547-13692A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811396 | ||||||
| chr6:109811668
|
G | A | 74 | a0001c0003t0001g0003a0001c0003t0001g0014a0001c0003t0001g0021others(71): Show | 74 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.2547-13420G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811668 | ||||||
| chr6:109811792
|
T | G | 1 | a0002c0004t0001g0178 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2547-13296T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811792 | ||||||
| chr6:109812112
|
G | A | 1 | a0002c0014t0002g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2547-12976G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812112 | ||||||
| chr6:109812291
|
A | G | 1 | a0002c0002t0005g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2547-12797A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812291 | ||||||
| chr6:109812364
|
G | C | 1 | a0001c0001t0002g0289 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2547-12724G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812364 | ||||||
| chr6:109812418
|
G | A | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2547-12670G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812418 | ||||||
| chr6:109812501
|
G | A | 196 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.2547-12587G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812501 | ||||||
| chr6:109812539
|
T | C | 1 | a0001c0003t0001g0020 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2547-12549T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812539 | ||||||
| chr6:109812661
|
T | C | 271 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(268): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.2547-12427T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812661 | ||||||
| chr6:109813051
|
C | T | 5 | a0002c0002t0002g0007a0002c0002t0002g0013a0002c0002t0005g0126others(2): Show | 5 | HG02559.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-12037C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813051 | ||||||
| chr6:109813446
|
G | T | 266 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.2547-11642G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813446 | ||||||
| chr6:109813577
|
T | C | 1 | a0001c0001t0002g0038 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2547-11511T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813577 | ||||||
| chr6:109813688
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2547-11400G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813688 | ||||||
| chr6:109813737
|
G | A | 26 | a0002c0002t0004g0006a0002c0002t0004g0123a0002c0002t0004g0186others(23): Show | 26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-11351G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813737 | ||||||
| chr6:109813905
|
C | T | 6 | a0001c0001t0003g0183a0002c0002t0002g0009a0002c0002t0002g0010others(3): Show | 6 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2547-11183C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813905 | ||||||
| chr6:109813906
|
G | A | 26 | a0002c0004t0001g0028a0002c0004t0001g0037a0002c0004t0001g0039others(23): Show | 26 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-11182G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813906 | ||||||
| chr6:109813945
|
G | A | 26 | a0002c0002t0004g0006a0002c0002t0004g0123a0002c0002t0004g0186others(23): Show | 26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-11143G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813945 | ||||||
| chr6:109814178
|
G | A | 5 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-10910G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109814178 | ||||||
| chr6:109814261
|
C | T | 2 | a0002c0002t0002g0117a0002c0002t0002g0118 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2547-10827C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109814261 | ||||||
| chr6:109814304
|
A | G | 7 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(4): Show | 7 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2547-10784A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109814304 | ||||||
| chr6:109814311
|
T | A | 2 | a0002c0002t0002g0012a0002c0009t0002g0158 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2547-10777T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109814311 | ||||||
| chr6:109814313
|
A | AT | 226 | a0001c0001t0002g0029a0001c0001t0002g0198a0001c0001t0002g0279others(223): Show | 228 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.2547-10767dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109814313 | |||||
| chr6:109814447
|
A | AT | 24 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0070others(21): Show | 24 | HG02004.hp1 HG02698.hp1 HG02965.hp2 others(21): Show |
intron_variant | MODIFIER | c.2547-10631dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109814447 | |||||
| chr6:109814447
|
AT | A | 228 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.2547-10631delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109814447 | |||||
| chr6:109814479
|
A | G | 1 | a0002c0002t0004g0356 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2547-10609A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109814479 | ||||||
| chr6:109815210
|
G | C | 1 | a0003c0005t0001g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2547-9878G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815210 | ||||||
| chr6:109815211
|
C | T | 1 | a0003c0005t0001g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2547-9877C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815211 | ||||||
| chr6:109815226
|
A | C | 264 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.2547-9862A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815226 | ||||||
| chr6:109815311
|
C | T | 1 | a0004c0006t0001g0344 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2547-9777C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815311 | ||||||
| chr6:109815377
|
C | T | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2547-9711C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815377 | ||||||
| chr6:109815393
|
C | G | 8 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(5): Show | 8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2547-9695C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815393 | ||||||
| chr6:109815495
|
G | GC | 51 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(48): Show | 52 | HG00438.hp1 HG00558.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.2547-9585dupC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109815495 | |||||
| chr6:109815496
|
C | CT | 175 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0014others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2547-9592_2547-959 others(5): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815496 | ||||||
| chr6:109815668
|
A | G | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2547-9420A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815668 | ||||||
| chr6:109815694
|
C | T | 177 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0014others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.2547-9394C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815694 | ||||||
| chr6:109815803
|
C | CA | 22 | a0002c0004t0001g0037a0002c0004t0001g0051a0002c0004t0001g0053others(19): Show | 22 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.2547-9276dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109815803 | |||||
| chr6:109815803
|
C | CAA | 7 | a0002c0004t0001g0028a0002c0004t0001g0039a0002c0004t0001g0040others(4): Show | 7 | HG02056.hp1 HG02071.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.2547-9277_2547-927 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109815803 | |||||
| chr6:109815935
|
A | G | 5 | a0002c0002t0002g0007a0002c0002t0002g0013a0002c0002t0005g0126others(2): Show | 5 | HG02559.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-9153A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815935 | ||||||
| chr6:109816109
|
G | A | 238 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2547-8979G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816109 | ||||||
| chr6:109816228
|
G | A | 177 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0014others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.2547-8860G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816228 | ||||||
| chr6:109816366
|
G | A | 1 | a0001c0001t0002g0096 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2547-8722G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816366 | ||||||
| chr6:109816513
|
C | T | 9 | a0001c0003t0001g0044a0001c0003t0001g0145a0001c0003t0001g0175others(6): Show | 9 | HG00408.hp2 HG02074.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.2547-8575C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816513 | ||||||
| chr6:109816590
|
A | G | 3 | a0001c0003t0001g0166a0001c0003t0001g0173a0001c0003t0001g0177 | 3 | HG00741.hp1 HG01978.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2547-8498A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816590 | ||||||
| chr6:109816673
|
A | G | 1 | a0002c0002t0004g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2547-8415A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816673 | ||||||
| chr6:109816778
|
G | A | 26 | a0002c0002t0004g0006a0002c0002t0004g0123a0002c0002t0004g0186others(23): Show | 26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-8310G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816778 | ||||||
| chr6:109816905
|
C | G | 1 | a0002c0014t0002g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2547-8183C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816905 | ||||||
| chr6:109816918
|
A | G | 8 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(5): Show | 8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2547-8170A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816918 | ||||||
| chr6:109816962
|
C | T | 2 | a0002c0004t0001g0231a0002c0004t0001g0232 | 2 | HG01361.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2547-8126C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816962 | ||||||
| chr6:109817063
|
T | C | 2 | a0002c0004t0001g0231a0002c0004t0001g0232 | 2 | HG01361.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2547-8025T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817063 | ||||||
| chr6:109817567
|
G | A | 150 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0014others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.2547-7521G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817567 | ||||||
| chr6:109817568
|
TA | T | 115 | a0001c0001t0002g0198a0001c0001t0002g0279a0001c0003t0001g0003others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.2547-7505delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109817568 | |||||
| chr6:109817569
|
A | T | 39 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(36): Show | 40 | HG00639.hp1 HG01255.hp2 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.2547-7519A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817569 | ||||||
| chr6:109817570
|
A | T | 1 | a0001c0003t0001g0266 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2547-7518A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817570 | ||||||
| chr6:109817675
|
C | T | 1 | a0002c0002t0002g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2547-7413C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817675 | ||||||
| chr6:109817786
|
G | T | 1 | a0001c0001t0002g0239 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2547-7302G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817786 | ||||||
| chr6:109817816
|
AG | A | 7 | a0001c0001t0002g0124a0001c0001t0002g0221a0001c0001t0002g0223others(4): Show | 7 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2547-7269delG | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109817816 | |||||
| chr6:109817854
|
G | A | 15 | a0002c0002t0002g0008a0002c0002t0002g0110a0002c0002t0002g0111others(12): Show | 15 | HG02257.hp2 HG02615.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.2547-7234G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817854 | ||||||
| chr6:109818202
|
CT | C | 14 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(11): Show | 14 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2547-6871delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109818202 | |||||
| chr6:109818264
|
G | A | 6 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0364others(3): Show | 6 | HG02615.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2547-6824G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818264 | ||||||
| chr6:109818452
|
G | A | 1 | a0002c0002t0004g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2547-6636G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818452 | ||||||
| chr6:109818480
|
A | C | 177 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0014others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.2547-6608A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818480 | ||||||
| chr6:109818493
|
C | T | 31 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0023others(28): Show | 32 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(29): Show |
intron_variant | MODIFIER | c.2547-6595C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818493 | ||||||
| chr6:109818496
|
G | A | 9 | a0002c0002t0004g0006a0002c0002t0004g0197a0002c0002t0004g0200others(6): Show | 9 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2547-6592G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818496 | ||||||
| chr6:109818649
|
T | C | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0083others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-6439T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818649 | ||||||
| chr6:109818723
|
C | T | 5 | a0002c0002t0002g0007a0002c0002t0002g0013a0002c0002t0005g0126others(2): Show | 5 | HG02559.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-6365C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818723 | ||||||
| chr6:109818773
|
G | C | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2547-6315G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818773 | ||||||
| chr6:109818872
|
A | C | 6 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(3): Show | 6 | NA18947.hp2 NA18949.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.2547-6216A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818872 | ||||||
| chr6:109819032
|
T | C | 2 | a0001c0003t0001g0170a0001c0003t0001g0172 | 2 | HG01081.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2547-6056T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819032 | ||||||
| chr6:109819043
|
C | A | 5 | a0002c0004t0001g0037a0002c0004t0001g0072a0002c0004t0001g0089others(2): Show | 5 | HG00099.hp1 HG02602.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-6045C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819043 | ||||||
| chr6:109819201
|
A | G | 32 | a0001c0001t0002g0104a0001c0001t0003g0001a0001c0001t0003g0022others(29): Show | 33 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(30): Show |
intron_variant | MODIFIER | c.2547-5887A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819201 | ||||||
| chr6:109819291
|
G | A | 2 | a0001c0001t0002g0267a0001c0001t0002g0268 | 2 | HG01071.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2547-5797G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819291 | ||||||
| chr6:109819634
|
A | G | 1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2547-5454A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819634 | ||||||
| chr6:109819823
|
T | G | 1 | a0004c0008t0002g0315 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2547-5265T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819823 | ||||||
| chr6:109819988
|
C | G | 11 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(8): Show | 11 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2547-5100C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819988 | ||||||
| chr6:109820027
|
G | C | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0083others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-5061G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820027 | ||||||
| chr6:109820038
|
G | A | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2547-5050G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820038 | ||||||
| chr6:109820086
|
G | A | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2547-5002G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820086 | ||||||
| chr6:109820096
|
G | A | 2 | a0002c0009t0002g0157a0002c0009t0002g0159 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2547-4992G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820096 | ||||||
| chr6:109820135
|
A | C | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2547-4953A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820135 | ||||||
| chr6:109820231
|
A | G | 2 | a0001c0003t0001g0319a0001c0003t0001g0368 | 2 | NA18969.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2547-4857A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820231 | ||||||
| chr6:109820287
|
A | T | 1 | a0002c0014t0002g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2547-4801A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820287 | ||||||
| chr6:109820409
|
C | T | 1 | a0004c0008t0002g0310 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2547-4679C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820409 | ||||||
| chr6:109820488
|
G | C | 215 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0023others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.2547-4600G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820488 | ||||||
| chr6:109820501
|
T | A | 1 | a0002c0002t0001g0136 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2547-4587T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820501 | ||||||
| chr6:109820506
|
G | A | 5 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0083others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-4582G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820506 | ||||||
| chr6:109820644
|
G | A | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2547-4444G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820644 | ||||||
| chr6:109820711
|
A | G | 2 | a0002c0002t0002g0115a0002c0002t0002g0116 | 2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2547-4377A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820711 | ||||||
| chr6:109820834
|
C | A | 1 | a0001c0001t0002g0241 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2547-4254C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820834 | ||||||
| chr6:109820908
|
G | A | 26 | a0002c0004t0001g0028a0002c0004t0001g0037a0002c0004t0001g0039others(23): Show | 26 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-4180G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820908 | ||||||
| chr6:109821077
|
A | C | 1 | a0001c0001t0002g0227 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2547-4011A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821077 | ||||||
| chr6:109821092
|
C | T | 2 | a0002c0004t0001g0128a0002c0004t0001g0129 | 2 | HG01255.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2547-3996C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821092 | ||||||
| chr6:109821112
|
C | T | 1 | a0001c0001t0002g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2547-3976C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821112 | ||||||
| chr6:109821362
|
A | C | 1 | a0001c0001t0003g0167 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2547-3726A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821362 | ||||||
| chr6:109821417
|
C | T | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2547-3671C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821417 | ||||||
| chr6:109821480
|
G | C | 1 | a0001c0001t0002g0088 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2547-3608G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821480 | ||||||
| chr6:109821507
|
A | G | 5 | a0001c0003t0001g0004a0001c0003t0001g0035a0001c0003t0001g0269others(2): Show | 5 | NA18943.hp2 NA18956.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-3581A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821507 | ||||||
| chr6:109821629
|
G | A | 206 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.2547-3459G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821629 | ||||||
| chr6:109821766
|
C | T | 1 | a0001c0001t0003g0193 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2547-3322C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821766 | ||||||
| chr6:109821769
|
A | G | 196 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.2547-3319A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821769 | ||||||
| chr6:109821784
|
G | A | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2547-3304G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821784 | ||||||
| chr6:109821901
|
T | C | 1 | a0002c0002t0004g0208 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2547-3187T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821901 | ||||||
| chr6:109822021
|
T | C | 5 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-3067T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822021 | ||||||
| chr6:109822211
|
A | G | 26 | a0001c0001t0002g0104a0001c0001t0003g0001a0001c0001t0003g0022others(23): Show | 27 | HG00438.hp1 HG00558.hp2 NA18939.hp1 others(24): Show |
intron_variant | MODIFIER | c.2547-2877A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822211 | ||||||
| chr6:109822364
|
TA | T | 179 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0014others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.2547-2718delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822364 | |||||
| chr6:109822755
|
GT | G | 5 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-2331delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822755 | |||||
| chr6:109822763
|
G | A | 265 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.2547-2325G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822763 | ||||||
| chr6:109822783
|
GTATGTAT others(3): Show |
G | 10 | a0001c0003t0001g0060a0002c0002t0001g0141a0002c0002t0001g0142others(7): Show | 10 | HG02071.hp1 HG02135.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.2547-2301_2547-229 others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | |||||
| chr6:109822783
|
GTATGTAT others(5): Show |
G | 21 | a0001c0003t0001g0024a0002c0002t0001g0132a0002c0002t0001g0133others(18): Show | 21 | HG00323.hp2 HG00544.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.2547-2301_2547-229 others(16): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | |||||
| chr6:109822783
|
GTATGTAT others(7): Show |
G | 31 | a0001c0003t0001g0170a0001c0003t0001g0172a0001c0003t0001g0173others(28): Show | 32 | HG00639.hp1 HG00741.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2547-2301_2547-228 others(18): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | |||||
| chr6:109822783
|
GTATGTAT others(9): Show |
G | 97 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0014others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.2547-2301_2547-228 others(20): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | |||||
| chr6:109822783
|
GTATGTAT others(11): Show |
G | 6 | a0001c0003t0001g0284a0002c0002t0002g0007a0002c0002t0002g0211others(3): Show | 6 | HG02109.hp1 HG02809.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2547-2301_2547-228 others(22): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | |||||
| chr6:109822783
|
GTATGTAT others(13): Show |
G | 5 | a0001c0001t0002g0279a0002c0002t0002g0013a0002c0002t0002g0084others(2): Show | 5 | HG02559.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-2301_2547-228 others(24): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | |||||
| chr6:109822783
|
GTATGTAT others(15): Show |
G | 15 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(12): Show | 15 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2547-2301_2547-228 others(26): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | |||||
| chr6:109822783
|
GTATGTAT others(21): Show |
G | 14 | a0002c0004t0001g0256a0003c0005t0001g0332a0003c0005t0001g0333others(11): Show | 14 | HG02155.hp2 NA18940.hp2 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.2547-2301_2547-227 others(32): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | |||||
| chr6:109822785
|
A | G | 3 | a0001c0003t0001g0252a0002c0002t0001g0130a0002c0002t0001g0135 | 3 | HG01943.hp1 NA18612.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.2547-2303A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822785 | ||||||
| chr6:109822786
|
TGTATATA others(6): Show |
T | 1 | a0002c0002t0001g0135 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2547-2301_2547-228 others(17): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822786 | ||||||
| chr6:109822787
|
G | GTA | 30 | a0001c0001t0002g0032a0001c0001t0002g0075a0001c0001t0002g0080others(27): Show | 31 | HG00741.hp2 HG01943.hp2 HG01993.hp2 others(28): Show |
intron_variant | MODIFIER | c.2547-2261_2547-226 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | |||||
| chr6:109822787
|
G | GTATA | 10 | a0001c0001t0002g0088a0001c0001t0002g0108a0001c0001t0002g0234others(7): Show | 10 | HG02738.hp2 HG03130.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.2547-2263_2547-226 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | |||||
| chr6:109822787
|
G | GTATATA | 6 | a0001c0001t0002g0074a0001c0001t0002g0094a0001c0001t0002g0098others(3): Show | 6 | HG00558.hp2 HG02300.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.2547-2265_2547-226 others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | |||||
| chr6:109822787
|
G | GTATATAT others(5): Show |
1 | a0002c0009t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2547-2271_2547-226 others(16): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | |||||
| chr6:109822787
|
GTA | G | 49 | a0001c0001t0002g0018a0001c0001t0002g0038a0001c0001t0002g0042others(46): Show | 49 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.2547-2261_2547-226 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | |||||
| chr6:109822787
|
GTATA | G | 27 | a0001c0001t0002g0122a0001c0001t0002g0214a0001c0001t0002g0235others(24): Show | 27 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.2547-2263_2547-226 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | |||||
| chr6:109822787
|
GTATATA | G | 6 | a0001c0001t0002g0030a0002c0002t0002g0119a0002c0002t0004g0186others(3): Show | 6 | HG01106.hp2 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2547-2265_2547-226 others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | |||||
| chr6:109822787
|
GTATATAT others(3): Show |
G | 1 | a0002c0002t0001g0130 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2547-2269_2547-226 others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | |||||
| chr6:109822787
|
GTATATAT others(9): Show |
G | 1 | a0001c0003t0001g0252 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2547-2275_2547-226 others(20): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | |||||
| chr6:109822789
|
A | G | 1 | a0005c0019t0006g0016 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2547-2299A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822789 | ||||||
| chr6:109822791
|
A | G | 2 | a0002c0002t0004g0204a0002c0002t0004g0357 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2547-2297A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822791 | ||||||
| chr6:109822793
|
A | G | 5 | a0002c0002t0001g0152a0002c0002t0004g0123a0002c0002t0004g0202others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-2295A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822793 | ||||||
| chr6:109822795
|
A | G | 26 | a0001c0003t0001g0060a0002c0002t0001g0141a0002c0002t0001g0142others(23): Show | 26 | HG01081.hp1 HG01243.hp2 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-2293A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822795 | ||||||
| chr6:109822797
|
A | G | 25 | a0001c0003t0001g0024a0002c0002t0001g0132a0002c0002t0001g0133others(22): Show | 25 | HG00323.hp2 HG00544.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.2547-2291A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822797 | ||||||
| chr6:109822799
|
A | G | 31 | a0001c0003t0001g0170a0001c0003t0001g0172a0001c0003t0001g0173others(28): Show | 32 | HG00639.hp1 HG00741.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2547-2289A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822799 | ||||||
| chr6:109822801
|
A | G | 97 | a0001c0003t0001g0003a0001c0003t0001g0004a0001c0003t0001g0014others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.2547-2287A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822801 | ||||||
| chr6:109822803
|
A | G | 6 | a0001c0003t0001g0284a0002c0002t0002g0007a0002c0002t0002g0211others(3): Show | 6 | HG02109.hp1 HG02809.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2547-2285A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822803 | ||||||
| chr6:109822805
|
A | G | 5 | a0001c0001t0002g0279a0002c0002t0002g0013a0002c0002t0002g0084others(2): Show | 5 | HG02559.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-2283A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822805 | ||||||
| chr6:109822807
|
A | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2547-2281A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822807 | ||||||
| chr6:109822813
|
A | G | 14 | a0002c0004t0001g0256a0003c0005t0001g0332a0003c0005t0001g0333others(11): Show | 14 | HG02155.hp2 NA18940.hp2 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.2547-2275A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822813 | ||||||
| chr6:109822829
|
C | T | 1 | a0001c0001t0003g0023 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2547-2259C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822829 | ||||||
| chr6:109822885
|
G | A | 1 | a0003c0005t0001g0343 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2547-2203G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822885 | ||||||
| chr6:109822912
|
G | GTA | 36 | a0001c0001t0002g0351a0001c0001t0002g0353a0001c0001t0003g0001others(33): Show | 38 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(35): Show |
intron_variant | MODIFIER | c.2547-2165_2547-216 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822912 | |||||
| chr6:109822925
|
C | T | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2547-2163C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822925 | ||||||
| chr6:109822931
|
ATC | A | 5 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-2154_2547-215 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822931 | |||||
| chr6:109823024
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2547-2064C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823024 | ||||||
| chr6:109823226
|
G | A | 26 | a0002c0004t0001g0028a0002c0004t0001g0037a0002c0004t0001g0039others(23): Show | 26 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-1862G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823226 | ||||||
| chr6:109823291
|
A | G | 1 | a0003c0005t0001g0250 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2547-1797A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823291 | ||||||
| chr6:109823459
|
G | A | 2 | a0002c0002t0002g0012a0002c0009t0002g0158 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2547-1629G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823459 | ||||||
| chr6:109823605
|
C | T | 31 | a0001c0001t0003g0001a0001c0001t0003g0022a0001c0001t0003g0023others(28): Show | 32 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(29): Show |
intron_variant | MODIFIER | c.2547-1483C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823605 | ||||||
| chr6:109823707
|
C | G | 1 | a0005c0019t0006g0016 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2547-1381C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823707 | ||||||
| chr6:109823816
|
T | A | 1 | a0001c0001t0002g0361 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2547-1272T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823816 | ||||||
| chr6:109823821
|
G | A | 26 | a0002c0004t0001g0028a0002c0004t0001g0037a0002c0004t0001g0039others(23): Show | 26 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-1267G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823821 | ||||||
| chr6:109823857
|
G | A | 2 | a0002c0009t0002g0157a0002c0009t0002g0159 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2547-1231G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823857 | ||||||
| chr6:109823919
|
C | G | 4 | a0002c0002t0002g0007a0002c0002t0002g0013a0002c0002t0005g0126others(1): Show | 4 | HG02559.hp1 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2547-1169C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823919 | ||||||
| chr6:109823984
|
G | A | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2547-1104G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823984 | ||||||
| chr6:109824097
|
CA | C | 5 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0029others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-989delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109824097 | |||||
| chr6:109824110
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2547-978G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824110 | ||||||
| chr6:109824170
|
G | A | 39 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0174others(36): Show | 40 | HG00639.hp1 HG01255.hp2 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.2547-918G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824170 | ||||||
| chr6:109824307
|
G | A | 1 | a0003c0005t0001g0312 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2547-781G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824307 | ||||||
| chr6:109824580
|
G | A | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2547-508G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824580 | ||||||
| chr6:109824587
|
C | T | 1 | a0001c0003t0001g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2547-501C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824587 | ||||||
| chr6:109824699
|
A | G | 1 | a0002c0014t0002g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2547-389A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824699 | ||||||
| chr6:109824817
|
C | T | 1 | a0001c0003t0001g0087 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2547-271C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824817 |