| geneid | 401024 |
|---|---|
| ensemblid | ENSG00000188738.16 |
| hgncid | 21675 |
| symbol | FSIP2 |
| name | fibrous sheath interacting protein 2 |
| refseq_nuc | NM_173651.4 |
| refseq_prot | NP_775922.3 |
| ensembl_nuc | ENST00000424728.6 |
| ensembl_prot | ENSP00000401306.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 185738804 |
| end | 185833290 |
| strand | + |
| ver | v1.2 |
| region | chr2:185738804-185833290 |
| region5000 | chr2:185733804-185838290 |
| regionname0 | FSIP2_chr2_185738804_185833290 |
| regionname5000 | FSIP2_chr2_185733804_185838290 |
| 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 | 0/0 | 6907 | 72 | 6 | 8 | 57 | 1 | 0 | 46 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0002 | 0/0 | 6907 | 49 | 4 | 6 | 37 | 0 | 2 | 28 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003 | 0/0 | 6907 | 44 | 16 | 11 | 9 | 0 | 8 | 5 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0004 | 0/0 | 6907 | 29 | 6 | 6 | 15 | 0 | 2 | 10 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0005 | 0/0 | 6907 | 26 | 2 | 11 | 4 | 1 | 8 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0006 | 0/0 | 6907 | 14 | 13 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0007 | 0/0 | 6907 | 10 | 0 | 4 | 6 | 0 | 0 | 4 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0008 | 0/1 | 6907 | 10 | 0 | 4 | 1 | 1 | 3 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0009 | 0/0 | 6907 | 8 | 0 | 7 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0010 | 0/0 | 6907 | 7 | 0 | 2 | 0 | 1 | 4 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0011 | 0/0 | 6907 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0012 | 0/0 | 6907 | 5 | 0 | 1 | 4 | 0 | 0 | 4 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0013 | 0/0 | 6907 | 5 | 0 | 4 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0014 | 0/0 | 6907 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0015 | 1/0 | 6907 | 5 | 4 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0016 | 0/0 | 6907 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0017 | 0/0 | 6907 | 5 | 0 | 0 | 0 | 3 | 2 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0018 | 0/0 | 6907 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0019 | 0/0 | 6907 | 4 | 0 | 1 | 3 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0020 | 0/0 | 6907 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0021 | 0/0 | 6907 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0022 | 0/0 | 6907 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0023 | 0/0 | 6907 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0024 | 0/0 | 6907 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0025 | 0/0 | 6907 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0026 | 0/0 | 6907 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0027 | 0/0 | 6907 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0028 | 0/0 | 6907 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0029 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0030 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0031 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0032 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0033 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0034 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0035 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0036 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0037 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0038 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0039 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0040 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0041 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0042 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0043 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0044 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0045 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0046 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0047 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0048 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0049 | 0/0 | 4105 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0050 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0051 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0052 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0053 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0054 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0055 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0056 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0057 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0058 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0059 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0060 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0061 | 0/0 | 6907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0062 | 0/0 | 6907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 20724 | 58 | 5 | 8 | 44 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0002 | 0/0 | 20724 | 42 | 3 | 6 | 31 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0003 | 0/0 | 20724 | 33 | 7 | 10 | 9 | 0 | 7 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0004 | 0/0 | 20724 | 26 | 6 | 6 | 12 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0005 | 0/0 | 20724 | 26 | 2 | 11 | 4 | 1 | 8 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0006 | 0/0 | 20724 | 13 | 12 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0007 | 0/0 | 20724 | 10 | 0 | 4 | 6 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0008 | 0/0 | 20724 | 8 | 0 | 0 | 8 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0009 | 0/0 | 20724 | 8 | 0 | 7 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0010 | 0/0 | 20724 | 7 | 0 | 4 | 1 | 1 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0011 | 0/0 | 20724 | 6 | 0 | 2 | 0 | 1 | 3 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0012 | 0/0 | 20724 | 6 | 6 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0013 | 0/0 | 20724 | 5 | 0 | 4 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0014 | 0/0 | 20724 | 5 | 5 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0015 | 1/0 | 20724 | 5 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0016 | 0/0 | 20724 | 5 | 0 | 1 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0017 | 0/0 | 20724 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0018 | 0/0 | 20724 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0019 | 0/0 | 20724 | 5 | 0 | 0 | 0 | 3 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0020 | 0/0 | 20724 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0021 | 0/0 | 20724 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0022 | 0/0 | 20724 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0023 | 0/0 | 20724 | 4 | 0 | 0 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0024 | 0/0 | 20724 | 4 | 0 | 1 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0025 | 0/0 | 20724 | 3 | 3 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0026 | 0/0 | 20724 | 3 | 0 | 0 | 0 | 0 | 3 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0027 | 0/1 | 20724 | 3 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0028 | 0/0 | 20724 | 3 | 3 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0029 | 0/0 | 20724 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0030 | 0/0 | 20724 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0031 | 0/0 | 20724 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0032 | 0/0 | 20724 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0033 | 0/0 | 20724 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0034 | 0/0 | 20724 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0035 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0036 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0037 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0038 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0039 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0040 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0041 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0042 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0043 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0044 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0045 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0046 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0047 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0048 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0049 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0050 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0051 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0052 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0053 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0054 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0055 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0056 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0057 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0058 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0059 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0060 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0061 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0062 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0063 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0064 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0065 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0066 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0067 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0068 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0069 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0070 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0071 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0072 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0073 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0074 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0075 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0076 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0077 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0078 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0079 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0080 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0081 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| c0082 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 156 | 235 | 57 | 54 | 91 | 7 | 25 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| t0002 | 0/1 | 157 | 127 | 25 | 20 | 65 | 3 | 13 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| t0003 | 0/0 | 156 | 7 | 7 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| t0004 | 0/0 | 156 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| 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 | 7 | 0 | 0 | 6 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0002 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0003 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0011 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0043 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 20724 | 58 | 5 | 8 | 44 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0001c0008 | 0/0 | 20724 | 8 | 0 | 0 | 8 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0001c0023 | 0/0 | 20724 | 4 | 0 | 0 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0001c0043 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0001c0051 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0002c0002 | 0/0 | 20724 | 42 | 3 | 6 | 31 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0002c0018 | 0/0 | 20724 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0002c0057 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0002c0062 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0003 | 0/0 | 20724 | 33 | 7 | 10 | 9 | 0 | 7 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0012 | 0/0 | 20724 | 6 | 6 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0066 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0072 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0075 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0076 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0081 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0004c0004 | 0/0 | 20724 | 26 | 6 | 6 | 12 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0004c0031 | 0/0 | 20724 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0004c0041 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0005c0005 | 0/0 | 20724 | 26 | 2 | 11 | 4 | 1 | 8 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0006c0006 | 0/0 | 20724 | 13 | 12 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0006c0069 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0007c0007 | 0/0 | 20724 | 10 | 0 | 4 | 6 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0008c0010 | 0/0 | 20724 | 7 | 0 | 4 | 1 | 1 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0008c0027 | 0/1 | 20724 | 3 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0009c0009 | 0/0 | 20724 | 8 | 0 | 7 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0010c0011 | 0/0 | 20724 | 6 | 0 | 2 | 0 | 1 | 3 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0010c0047 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0011c0017 | 0/0 | 20724 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0012c0016 | 0/0 | 20724 | 5 | 0 | 1 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0013c0013 | 0/0 | 20724 | 5 | 0 | 4 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0014c0014 | 0/0 | 20724 | 5 | 5 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0015c0015 | 1/0 | 20724 | 5 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0016c0022 | 0/0 | 20724 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0016c0038 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0017c0019 | 0/0 | 20724 | 5 | 0 | 0 | 0 | 3 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0018c0021 | 0/0 | 20724 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0019c0024 | 0/0 | 20724 | 4 | 0 | 1 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0020c0020 | 0/0 | 20724 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0021c0026 | 0/0 | 20724 | 3 | 0 | 0 | 0 | 0 | 3 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0022c0025 | 0/0 | 20724 | 3 | 3 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0023c0028 | 0/0 | 20724 | 3 | 3 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0024c0034 | 0/0 | 20724 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0024c0082 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0025c0030 | 0/0 | 20724 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0026c0029 | 0/0 | 20724 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0027c0033 | 0/0 | 20724 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0028c0032 | 0/0 | 20724 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0029c0039 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0030c0044 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0031c0040 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0032c0045 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0033c0035 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0034c0050 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0035c0042 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0036c0049 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0037c0048 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0038c0052 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0039c0046 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0040c0053 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0041c0054 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0042c0077 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0043c0036 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0044c0068 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0045c0067 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0046c0071 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0047c0074 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0048c0073 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0049c0070 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0050c0065 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0051c0064 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0052c0060 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0053c0059 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0054c0058 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0055c0056 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0056c0061 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0057c0055 | 0/0 | 20724 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0058c0063 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0059c0078 | 0/0 | 20724 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0060c0079 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0061c0037 | 0/0 | 20724 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0062c0080 | 0/0 | 20724 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 20880 | 58 | 5 | 8 | 44 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0001c0008t0002 | 0/0 | 20880 | 8 | 0 | 0 | 8 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0001c0023t0002 | 0/0 | 20880 | 4 | 0 | 0 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0001c0043t0002 | 0/0 | 20880 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0001c0051t0002 | 0/0 | 20880 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0002c0002t0001 | 0/0 | 20879 | 42 | 3 | 6 | 31 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0002c0018t0001 | 0/0 | 20879 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0002c0057t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0002c0062t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0003t0001 | 0/0 | 20879 | 33 | 7 | 10 | 9 | 0 | 7 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0012t0001 | 0/0 | 20879 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0012t0003 | 0/0 | 20879 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0066t0001 | 0/0 | 20879 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0072t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0075t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0076t0001 | 0/0 | 20879 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0003c0081t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0004c0004t0001 | 0/0 | 20879 | 19 | 3 | 6 | 8 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0004c0004t0002 | 0/0 | 20880 | 6 | 2 | 0 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0004c0004t0004 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0004c0031t0002 | 0/0 | 20880 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0004c0041t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0005c0005t0001 | 0/0 | 20879 | 26 | 2 | 11 | 4 | 1 | 8 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0006c0006t0001 | 0/0 | 20879 | 12 | 11 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0006c0006t0002 | 0/0 | 20880 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0006c0069t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0007c0007t0001 | 0/0 | 20879 | 10 | 0 | 4 | 6 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0008c0010t0002 | 0/0 | 20880 | 7 | 0 | 4 | 1 | 1 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0008c0027t0002 | 0/1 | 20880 | 3 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0009c0009t0001 | 0/0 | 20879 | 8 | 0 | 7 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0010c0011t0002 | 0/0 | 20880 | 6 | 0 | 2 | 0 | 1 | 3 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0010c0047t0002 | 0/0 | 20880 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0011c0017t0001 | 0/0 | 20879 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0012c0016t0001 | 0/0 | 20879 | 5 | 0 | 1 | 4 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0013c0013t0002 | 0/0 | 20880 | 5 | 0 | 4 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0014c0014t0002 | 0/0 | 20880 | 5 | 5 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0015c0015t0001 | 1/0 | 20879 | 5 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0016c0022t0002 | 0/0 | 20880 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0016c0038t0002 | 0/0 | 20880 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0017c0019t0001 | 0/0 | 20879 | 5 | 0 | 0 | 0 | 3 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0018c0021t0001 | 0/0 | 20879 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0019c0024t0001 | 0/0 | 20879 | 4 | 0 | 1 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0020c0020t0003 | 0/0 | 20879 | 4 | 4 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0021c0026t0002 | 0/0 | 20880 | 3 | 0 | 0 | 0 | 0 | 3 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0022c0025t0001 | 0/0 | 20879 | 3 | 3 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0023c0028t0001 | 0/0 | 20879 | 3 | 3 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0024c0034t0001 | 0/0 | 20879 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0024c0082t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0025c0030t0002 | 0/0 | 20880 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0026c0029t0002 | 0/0 | 20880 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0027c0033t0001 | 0/0 | 20879 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0028c0032t0001 | 0/0 | 20879 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0029c0039t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0030c0044t0002 | 0/0 | 20880 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0031c0040t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0032c0045t0002 | 0/0 | 20880 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0033c0035t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0034c0050t0002 | 0/0 | 20880 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0035c0042t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0036c0049t0002 | 0/0 | 20880 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0037c0048t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0038c0052t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0039c0046t0002 | 0/0 | 20880 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0040c0053t0002 | 0/0 | 20880 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0041c0054t0002 | 0/0 | 20880 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0042c0077t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0043c0036t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0044c0068t0001 | 0/0 | 20879 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0045c0067t0001 | 0/0 | 20879 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0046c0071t0001 | 0/0 | 20879 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0047c0074t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0048c0073t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0049c0070t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0050c0065t0001 | 0/0 | 20879 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0051c0064t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0052c0060t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0053c0059t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0054c0058t0001 | 0/0 | 20879 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0055c0056t0001 | 0/0 | 20879 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0056c0061t0001 | 0/0 | 20879 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0057c0055t0001 | 0/0 | 20879 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0058c0063t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0059c0078t0001 | 0/0 | 20879 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0060c0079t0001 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0061c0037t0001 | 0/0 | 20879 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| a0062c0080t0003 | 0/0 | 20879 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | copy fasta | chr2 | 185733804 | 185838290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0003 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0008t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0008t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0008t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0008t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0023t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0023t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0023t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0043t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0001c0051t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0018t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0018t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0018t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0018t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0057t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0002c0062t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0012t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0012t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0012t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0012t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0012t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0012t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0066t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0072t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0075t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0076t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0003c0081t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0004t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0031t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0031t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0004c0041t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0011 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0005c0005t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0006c0006t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0006c0006t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0006c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0006c0006t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0006c0006t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0006c0006t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0006c0006t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0006c0006t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0006c0006t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0006c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0006c0006t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0006c0069t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0007c0007t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0007c0007t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0007c0007t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0007c0007t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0007c0007t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0007c0007t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0007c0007t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0007c0007t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0007c0007t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0007c0007t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0008c0010t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0008c0010t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0008c0010t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0008c0010t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0008c0010t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0008c0010t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0008c0010t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0008c0027t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0008c0027t0002g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0008c0027t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0009c0009t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0009c0009t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0009c0009t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0009c0009t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0009c0009t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0009c0009t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0010c0011t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0010c0011t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0010c0011t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0010c0011t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0010c0011t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0010c0011t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0010c0047t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0011c0017t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0011c0017t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0011c0017t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0011c0017t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0012c0016t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0012c0016t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0012c0016t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0012c0016t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0012c0016t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0013c0013t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0013c0013t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0013c0013t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0013c0013t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0013c0013t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0014c0014t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0014c0014t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0014c0014t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0014c0014t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0014c0014t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0015c0015t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0015c0015t0001g0043 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0015c0015t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0015c0015t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0015c0015t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0016c0022t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0016c0022t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0016c0022t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0016c0022t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0016c0038t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0017c0019t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0017c0019t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0017c0019t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0017c0019t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0018c0021t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0018c0021t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0018c0021t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0019c0024t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0019c0024t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0019c0024t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0019c0024t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0020c0020t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0020c0020t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0020c0020t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0021c0026t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0021c0026t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0022c0025t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0022c0025t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0023c0028t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0023c0028t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0024c0034t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0024c0034t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0024c0082t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0025c0030t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0025c0030t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0026c0029t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0026c0029t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0027c0033t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0027c0033t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0028c0032t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0029c0039t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0030c0044t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0031c0040t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0032c0045t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0033c0035t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0034c0050t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0035c0042t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0036c0049t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0037c0048t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0038c0052t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0039c0046t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0040c0053t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0041c0054t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0042c0077t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0043c0036t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0044c0068t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0045c0067t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0046c0071t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0047c0074t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0048c0073t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0049c0070t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0050c0065t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0051c0064t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0052c0060t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0053c0059t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0054c0058t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0055c0056t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0056c0061t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0057c0055t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0058c0063t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0059c0078t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0060c0079t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0061c0037t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| a0062c0080t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0044 | c0068 | t0001 | g0285 | EUR | GBR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00099 | hp2 | a0010 | c0011 | t0002 | g0106 | EUR | GBR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00280 | hp1 | a0017 | c0019 | t0001 | g0204 | EUR | FIN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00280 | hp2 | a0045 | c0067 | t0001 | g0283 | EUR | FIN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0161 | EUR | FIN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00323 | hp2 | a0017 | c0019 | t0001 | g0202 | EUR | FIN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00423 | hp2 | a0007 | c0007 | t0001 | g0046 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00544 | hp1 | a0004 | c0004 | t0001 | g0071 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00544 | hp2 | a0019 | c0024 | t0001 | g0238 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00558 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00597 | hp2 | a0019 | c0024 | t0001 | g0236 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0246 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00639 | hp2 | a0027 | c0033 | t0001 | g0311 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00642 | hp1 | a0005 | c0005 | t0001 | g0290 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0229 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00733 | hp1 | a0003 | c0066 | t0001 | g0288 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00733 | hp2 | a0055 | c0056 | t0001 | g0041 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00735 | hp1 | a0008 | c0010 | t0002 | g0097 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00735 | hp2 | a0003 | c0003 | t0001 | g0220 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00738 | hp1 | a0004 | c0004 | t0001 | g0067 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00738 | hp2 | a0005 | c0005 | t0001 | g0281 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00741 | hp1 | a0010 | c0011 | t0002 | g0109 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01070 | hp1 | a0008 | c0010 | t0002 | g0096 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01070 | hp2 | a0005 | c0005 | t0001 | g0292 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01071 | hp1 | a0005 | c0005 | t0001 | g0291 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01071 | hp2 | a0008 | c0010 | t0002 | g0088 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0014 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01099 | hp1 | a0006 | c0006 | t0001 | g0274 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01099 | hp2 | a0005 | c0005 | t0001 | g0301 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01106 | hp1 | a0003 | c0003 | t0001 | g0227 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01106 | hp2 | a0010 | c0011 | t0002 | g0105 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0228 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01109 | hp2 | a0013 | c0013 | t0002 | g0121 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01167 | hp1 | a0027 | c0033 | t0001 | g0224 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01167 | hp2 | a0009 | c0009 | t0001 | g0012 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01168 | hp1 | a0004 | c0004 | t0001 | g0074 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01168 | hp2 | a0013 | c0013 | t0002 | g0147 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01169 | hp1 | a0004 | c0004 | t0001 | g0073 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01169 | hp2 | a0009 | c0009 | t0001 | g0293 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01175 | hp1 | a0005 | c0005 | t0001 | g0032 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01175 | hp2 | a0013 | c0013 | t0002 | g0149 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01192 | hp2 | a0050 | c0065 | t0001 | g0287 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01243 | hp1 | a0003 | c0003 | t0001 | g0208 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01243 | hp2 | a0004 | c0004 | t0001 | g0078 | AMR | PUR | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01255 | hp2 | a0054 | c0058 | t0001 | g0261 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0025 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01256 | hp2 | a0004 | c0004 | t0001 | g0082 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0025 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01258 | hp2 | a0039 | c0046 | t0002 | g0176 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01261 | hp1 | a0012 | c0016 | t0001 | g0059 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01261 | hp2 | a0005 | c0005 | t0001 | g0303 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01346 | hp2 | a0007 | c0007 | t0001 | g0051 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01361 | hp2 | a0005 | c0005 | t0001 | g0282 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01496 | hp1 | a0057 | c0055 | t0001 | g0280 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01516 | hp1 | a0005 | c0005 | t0001 | g0032 | EUR | IBS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01516 | hp2 | a0008 | c0010 | t0002 | g0095 | EUR | IBS | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01884 | hp2 | a0004 | c0004 | t0001 | g0066 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01891 | hp1 | a0020 | c0020 | t0003 | g0063 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01891 | hp2 | a0015 | c0015 | t0001 | g0002 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01928 | hp1 | a0009 | c0009 | t0001 | g0299 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01943 | hp1 | a0007 | c0007 | t0001 | g0054 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01952 | hp1 | a0007 | c0007 | t0001 | g0052 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01952 | hp2 | a0005 | c0005 | t0001 | g0300 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01975 | hp1 | a0007 | c0007 | t0001 | g0053 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01975 | hp2 | a0004 | c0004 | t0001 | g0077 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01978 | hp1 | a0005 | c0005 | t0001 | g0011 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01978 | hp2 | a0013 | c0013 | t0002 | g0130 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01981 | hp1 | a0041 | c0054 | t0002 | g0169 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01981 | hp2 | a0009 | c0009 | t0001 | g0012 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02004 | hp2 | a0009 | c0009 | t0001 | g0298 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02015 | hp1 | a0042 | c0077 | t0001 | g0218 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02015 | hp2 | a0005 | c0005 | t0001 | g0296 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02055 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02055 | hp2 | a0049 | c0070 | t0001 | g0271 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02056 | hp2 | a0004 | c0004 | t0001 | g0005 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02071 | hp2 | a0019 | c0024 | t0001 | g0258 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02074 | hp1 | a0005 | c0005 | t0001 | g0304 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02080 | hp2 | a0001 | c0008 | t0002 | g0004 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02083 | hp1 | a0059 | c0078 | t0001 | g0289 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02083 | hp2 | a0001 | c0008 | t0002 | g0146 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0216 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02135 | hp2 | a0003 | c0003 | t0001 | g0230 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02145 | hp1 | a0023 | c0028 | t0001 | g0302 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02145 | hp2 | a0032 | c0045 | t0002 | g0120 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02148 | hp1 | a0009 | c0009 | t0001 | g0294 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02148 | hp2 | a0019 | c0024 | t0001 | g0239 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | CDX | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CDX | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02165 | hp1 | a0004 | c0041 | t0001 | g0083 | EAS | CDX | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | CDX | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02257 | hp2 | a0014 | c0014 | t0002 | g0111 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02258 | hp1 | a0003 | c0081 | t0001 | g0206 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02258 | hp2 | a0015 | c0015 | t0001 | g0064 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02273 | hp2 | a0005 | c0005 | t0001 | g0286 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02280 | hp1 | a0006 | c0006 | t0001 | g0279 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02280 | hp2 | a0043 | c0036 | t0001 | g0194 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02293 | hp1 | a0009 | c0009 | t0001 | g0012 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02300 | hp2 | a0003 | c0003 | t0001 | g0014 | AMR | PEL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02523 | hp1 | a0004 | c0004 | t0001 | g0069 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02523 | hp2 | a0001 | c0008 | t0002 | g0004 | EAS | KHV | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02572 | hp1 | a0006 | c0006 | t0001 | g0273 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02572 | hp2 | a0003 | c0003 | t0001 | g0207 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02602 | hp1 | a0010 | c0011 | t0002 | g0107 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0209 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02615 | hp1 | a0006 | c0006 | t0001 | g0276 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02615 | hp2 | a0014 | c0014 | t0002 | g0103 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02630 | hp1 | a0016 | c0022 | t0002 | g0182 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02630 | hp2 | a0014 | c0014 | t0002 | g0110 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02647 | hp1 | a0062 | c0080 | t0003 | g0038 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02647 | hp2 | a0003 | c0072 | t0001 | g0184 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02698 | hp1 | a0005 | c0005 | t0001 | g0035 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02698 | hp2 | a0021 | c0026 | t0002 | g0087 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02717 | hp1 | a0022 | c0025 | t0001 | g0188 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02717 | hp2 | a0018 | c0021 | t0001 | g0198 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02723 | hp1 | a0060 | c0079 | t0001 | g0191 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02723 | hp2 | a0006 | c0006 | t0001 | g0030 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02735 | hp1 | a0005 | c0005 | t0001 | g0035 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02735 | hp2 | a0036 | c0049 | t0002 | g0122 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02738 | hp1 | a0010 | c0011 | t0002 | g0099 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02738 | hp2 | a0003 | c0076 | t0001 | g0265 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02809 | hp2 | a0020 | c0020 | t0003 | g0062 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02818 | hp1 | a0016 | c0022 | t0002 | g0180 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02818 | hp2 | a0003 | c0012 | t0001 | g0192 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02886 | hp1 | a0006 | c0006 | t0001 | g0031 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02886 | hp2 | a0034 | c0050 | t0002 | g0018 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02895 | hp1 | a0022 | c0025 | t0001 | g0022 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02895 | hp2 | a0003 | c0012 | t0001 | g0193 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02896 | hp1 | a0015 | c0015 | t0001 | g0050 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02896 | hp2 | a0004 | c0004 | t0001 | g0081 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02897 | hp1 | a0022 | c0025 | t0001 | g0022 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02897 | hp2 | a0015 | c0015 | t0001 | g0048 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0269 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02922 | hp2 | a0018 | c0021 | t0001 | g0197 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02965 | hp1 | a0018 | c0021 | t0001 | g0023 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02965 | hp2 | a0020 | c0020 | t0003 | g0013 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02970 | hp1 | a0006 | c0006 | t0001 | g0031 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02970 | hp2 | a0003 | c0012 | t0001 | g0190 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02976 | hp1 | a0006 | c0006 | t0001 | g0270 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02976 | hp2 | a0023 | c0028 | t0001 | g0034 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0205 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03017 | hp2 | a0056 | c0061 | t0001 | g0247 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03041 | hp1 | a0016 | c0038 | t0002 | g0181 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03041 | hp2 | a0026 | c0029 | t0002 | g0170 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03098 | hp1 | a0003 | c0012 | t0003 | g0039 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03098 | hp2 | a0048 | c0073 | t0001 | g0275 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03130 | hp1 | a0025 | c0030 | t0002 | g0116 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0267 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03139 | hp1 | a0033 | c0035 | t0001 | g0042 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03139 | hp2 | a0025 | c0030 | t0002 | g0183 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03195 | hp1 | a0016 | c0022 | t0002 | g0179 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03195 | hp2 | a0023 | c0028 | t0001 | g0034 | AFR | ESN | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03209 | hp2 | a0003 | c0075 | t0001 | g0189 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03225 | hp1 | a0016 | c0022 | t0002 | g0178 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0199 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03239 | hp2 | a0021 | c0026 | t0002 | g0015 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03453 | hp1 | a0037 | c0048 | t0001 | g0186 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03453 | hp2 | a0006 | c0006 | t0001 | g0030 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03486 | hp1 | a0003 | c0012 | t0001 | g0195 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03486 | hp2 | a0004 | c0004 | t0004 | g0075 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03490 | hp1 | a0046 | c0071 | t0001 | g0221 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03490 | hp2 | a0008 | c0027 | t0002 | g0090 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03491 | hp1 | a0061 | c0037 | t0001 | g0001 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03491 | hp2 | a0017 | c0019 | t0001 | g0024 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03492 | hp1 | a0017 | c0019 | t0001 | g0024 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03492 | hp2 | a0008 | c0027 | t0002 | g0093 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03540 | hp1 | a0004 | c0004 | t0001 | g0072 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03540 | hp2 | a0006 | c0006 | t0002 | g0177 | AFR | GWD | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03579 | hp1 | a0006 | c0006 | t0001 | g0277 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03579 | hp2 | a0004 | c0004 | t0002 | g0021 | AFR | MSL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03654 | hp1 | a0013 | c0013 | t0002 | g0140 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03654 | hp2 | a0004 | c0004 | t0001 | g0076 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03688 | hp1 | a0005 | c0005 | t0001 | g0033 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03688 | hp2 | a0010 | c0011 | t0002 | g0117 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03710 | hp1 | a0005 | c0005 | t0001 | g0295 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03710 | hp2 | a0021 | c0026 | t0002 | g0015 | SAS | PJL | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03831 | hp1 | a0005 | c0005 | t0001 | g0033 | SAS | BEB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0233 | SAS | BEB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03942 | hp1 | a0010 | c0047 | t0002 | g0115 | SAS | BEB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0310 | SAS | BEB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG04115 | hp1 | a0005 | c0005 | t0001 | g0284 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG04115 | hp2 | a0004 | c0004 | t0001 | g0065 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0211 | SAS | BEB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG04184 | hp2 | a0030 | c0044 | t0002 | g0153 | SAS | BEB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0210 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG04199 | hp2 | a0008 | c0010 | t0002 | g0091 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG04204 | hp1 | a0005 | c0005 | t0001 | g0307 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0232 | SAS | STU | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18522 | hp1 | a0001 | c0051 | t0002 | g0104 | AFR | YRI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18522 | hp2 | a0020 | c0020 | t0003 | g0013 | AFR | YRI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18612 | hp1 | a0003 | c0003 | t0001 | g0226 | EAS | CHB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | CHB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0222 | EAS | CHB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18747 | hp2 | a0007 | c0007 | t0001 | g0060 | EAS | CHB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18906 | hp1 | a0006 | c0069 | t0001 | g0272 | AFR | YRI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | YRI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18940 | hp1 | a0004 | c0004 | t0001 | g0070 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18944 | hp1 | a0011 | c0017 | t0001 | g0055 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18946 | hp1 | a0007 | c0007 | t0001 | g0045 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18948 | hp1 | a0012 | c0016 | t0001 | g0002 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18949 | hp1 | a0004 | c0031 | t0002 | g0168 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18951 | hp2 | a0007 | c0007 | t0001 | g0049 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18952 | hp1 | a0005 | c0005 | t0001 | g0297 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18953 | hp2 | a0004 | c0004 | t0002 | g0174 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18959 | hp1 | a0001 | c0043 | t0002 | g0127 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18959 | hp2 | a0024 | c0034 | t0001 | g0237 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18961 | hp2 | a0028 | c0032 | t0001 | g0029 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18964 | hp2 | a0007 | c0007 | t0001 | g0061 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18965 | hp2 | a0053 | c0059 | t0001 | g0001 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18967 | hp1 | a0004 | c0004 | t0002 | g0019 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18970 | hp2 | a0004 | c0004 | t0001 | g0068 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18972 | hp2 | a0011 | c0017 | t0001 | g0002 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18979 | hp2 | a0003 | c0003 | t0001 | g0215 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0223 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18981 | hp1 | a0002 | c0018 | t0001 | g0241 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18981 | hp2 | a0001 | c0023 | t0002 | g0136 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18984 | hp2 | a0002 | c0018 | t0001 | g0260 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18986 | hp1 | a0001 | c0008 | t0002 | g0004 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18986 | hp2 | a0012 | c0016 | t0001 | g0057 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18989 | hp1 | a0011 | c0017 | t0001 | g0047 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18989 | hp2 | a0035 | c0042 | t0001 | g0079 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18990 | hp1 | a0011 | c0017 | t0001 | g0044 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18990 | hp2 | a0001 | c0008 | t0002 | g0160 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18991 | hp2 | a0001 | c0008 | t0002 | g0144 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18992 | hp1 | a0004 | c0031 | t0002 | g0167 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18993 | hp1 | a0007 | c0007 | t0001 | g0002 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18993 | hp2 | a0051 | c0064 | t0001 | g0243 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18998 | hp1 | a0001 | c0023 | t0002 | g0017 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18998 | hp2 | a0003 | c0003 | t0001 | g0213 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18999 | hp2 | a0002 | c0018 | t0001 | g0027 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19001 | hp1 | a0008 | c0010 | t0002 | g0128 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19002 | hp1 | a0005 | c0005 | t0001 | g0201 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19002 | hp2 | a0047 | c0074 | t0001 | g0212 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19003 | hp1 | a0001 | c0023 | t0002 | g0138 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19003 | hp2 | a0002 | c0057 | t0001 | g0250 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19004 | hp2 | a0024 | c0082 | t0001 | g0240 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19007 | hp2 | a0052 | c0060 | t0001 | g0006 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19009 | hp2 | a0001 | c0008 | t0002 | g0004 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19030 | hp1 | a0006 | c0006 | t0001 | g0268 | AFR | LWK | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0266 | AFR | LWK | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0203 | AFR | LWK | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | LWK | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19054 | hp2 | a0001 | c0023 | t0002 | g0017 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19056 | hp1 | a0040 | c0053 | t0002 | g0007 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19056 | hp2 | a0002 | c0018 | t0001 | g0027 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19060 | hp1 | a0003 | c0003 | t0001 | g0214 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19065 | hp1 | a0011 | c0017 | t0001 | g0002 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19065 | hp2 | a0031 | c0040 | t0001 | g0005 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19070 | hp1 | a0004 | c0004 | t0001 | g0080 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19070 | hp2 | a0028 | c0032 | t0001 | g0029 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19075 | hp1 | a0004 | c0004 | t0002 | g0173 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19077 | hp2 | a0012 | c0016 | t0001 | g0056 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19079 | hp2 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19080 | hp2 | a0004 | c0004 | t0002 | g0019 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19084 | hp2 | a0002 | c0018 | t0001 | g0242 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19085 | hp2 | a0012 | c0016 | t0001 | g0058 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19088 | hp2 | a0001 | c0008 | t0002 | g0004 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19089 | hp2 | a0024 | c0034 | t0001 | g0037 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19091 | hp2 | a0003 | c0003 | t0001 | g0254 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19240 | hp1 | a0006 | c0006 | t0001 | g0278 | AFR | YRI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA19240 | hp2 | a0014 | c0014 | t0002 | g0102 | AFR | YRI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA20129 | hp1 | a0003 | c0012 | t0003 | g0040 | AFR | ASW | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA20129 | hp2 | a0014 | c0014 | t0002 | g0101 | AFR | ASW | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA20752 | hp1 | a0017 | c0019 | t0001 | g0217 | EUR | TSI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA20752 | hp2 | a0009 | c0009 | t0001 | g0306 | EUR | TSI | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA20905 | hp1 | a0005 | c0005 | t0001 | g0011 | SAS | GIH | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0308 | SAS | GIH | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01123 | hp1 | a0003 | c0003 | t0001 | g0309 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG01123 | hp2 | a0008 | c0010 | t0002 | g0094 | AMR | CLM | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02109 | hp1 | a0026 | c0029 | t0002 | g0100 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02486 | hp1 | a0005 | c0005 | t0001 | g0305 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02486 | hp2 | a0004 | c0004 | t0002 | g0021 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02559 | hp1 | a0002 | c0062 | t0001 | g0231 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0264 | AFR | ACB | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18955 | hp1 | a0058 | c0063 | t0001 | g0006 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA20300 | hp1 | a0038 | c0052 | t0001 | g0187 | AFR | USA | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA20300 | hp2 | a0018 | c0021 | t0001 | g0023 | AFR | USA | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA21309 | hp1 | a0003 | c0003 | t0001 | g0225 | AFR | LWK | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| NA21309 | hp2 | a0029 | c0039 | t0001 | g0196 | AFR | LWK | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| homoSapiens_chm13v2 | hp1 | a0008 | c0027 | t0002 | g0092 | REF | REF | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| homoSapiens_grch38 | hp1 | a0015 | c0015 | t0001 | g0043 | REF | REF | FSIP2_chr2_185733804_185838290 | FSIP2 | chr2 | 185733804 | 185838290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:185745439
|
C | G | 1 | a0024 | 3 | NA18959.hp2 NA19004.hp2 NA19089.hp2 |
missense_variant | MODERATE | c.488C>G | p.Ala163Gly | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/23 | 579/20879 | 488/20724 | 163/6907 | chr2 | 185745439 | ||
| chr2:185746763
|
C | T | 1 | a0023 | 3 | HG02145.hp1 HG02976.hp2 HG03195.hp2 |
missense_variant | MODERATE | c.712C>T | p.Arg238Trp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 6/23 | 803/20879 | 712/20724 | 238/6907 | chr2 | 185746763 | ||
| chr2:185753767
|
A | G | 2 | a0020a0062 | 5 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
missense_variant | MODERATE | c.916A>G | p.Met306Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/23 | 1007/20879 | 916/20724 | 306/6907 | chr2 | 185753767 | ||
| chr2:185753824
|
G | A | 1 | a0061 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.973G>A | p.Gly325Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/23 | 1064/20879 | 973/20724 | 325/6907 | chr2 | 185753824 | ||
| chr2:185761994
|
A | C | 1 | a0060 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1217A>C | p.Asn406Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/23 | 1308/20879 | 1217/20724 | 406/6907 | chr2 | 185761994 | ||
| chr2:185761994
|
A | T | 1 | a0029 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1217A>T | p.Asn406Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/23 | 1308/20879 | 1217/20724 | 406/6907 | chr2 | 185761994 | ||
| chr2:185763216
|
T | C | 34 | a0002a0003a0005others(31): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.1274T>C | p.Ile425Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/23 | 1365/20879 | 1274/20724 | 425/6907 | chr2 | 185763216 | ||
| chr2:185789591
|
A | T | 3 | a0007a0011a0012 | 20 | HG00423.hp2 HG01261.hp1 HG01346.hp2 others(17): Show |
missense_variant | MODERATE | c.2455A>T | p.Ile819Phe | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 2546/20879 | 2455/20724 | 819/6907 | chr2 | 185789591 | ||
| chr2:185789748
|
A | G | 1 | a0059 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.2612A>G | p.Asn871Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 2703/20879 | 2612/20724 | 871/6907 | chr2 | 185789748 | ||
| chr2:185789789
|
A | G | 1 | a0042 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.2653A>G | p.Asn885Asp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 2744/20879 | 2653/20724 | 885/6907 | chr2 | 185789789 | ||
| chr2:185789865
|
A | G | 34 | a0002a0003a0005others(31): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.2729A>G | p.Asn910Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 2820/20879 | 2729/20724 | 910/6907 | chr2 | 185789865 | ||
| chr2:185790140
|
G | C | 13 | a0002a0019a0024others(10): Show | 67 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(64): Show |
missense_variant | MODERATE | c.3004G>C | p.Asp1002His | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 3095/20879 | 3004/20724 | 1002/6907 | chr2 | 185790140 | ||
| chr2:185790396
|
C | T | 1 | a0051 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.3260C>T | p.Ser1087Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 3351/20879 | 3260/20724 | 1087/6907 | chr2 | 185790396 | ||
| chr2:185790509
|
C | T | 1 | a0058 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.3373C>T | p.Pro1125Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 3464/20879 | 3373/20724 | 1125/6907 | chr2 | 185790509 | ||
| chr2:185790849
|
T | C | 1 | a0030 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.3713T>C | p.Val1238Ala | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 3804/20879 | 3713/20724 | 1238/6907 | chr2 | 185790849 | ||
| chr2:185790930
|
G | A | 1 | a0021 | 3 | HG02698.hp2 HG03239.hp2 HG03710.hp2 |
missense_variant | MODERATE | c.3794G>A | p.Arg1265His | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 3885/20879 | 3794/20724 | 1265/6907 | chr2 | 185790930 | ||
| chr2:185790999
|
G | A | 57 | a0001a0002a0003others(54): Show | 344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
missense_variant | MODERATE | c.3863G>A | p.Arg1288Gln | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 3954/20879 | 3863/20724 | 1288/6907 | chr2 | 185790999 | ||
| chr2:185791173
|
C | T | 1 | a0016 | 5 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
missense_variant | MODERATE | c.4037C>T | p.Thr1346Met | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 4128/20879 | 4037/20724 | 1346/6907 | chr2 | 185791173 | ||
| chr2:185791278
|
G | A | 1 | a0031 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.4142G>A | p.Arg1381His | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 4233/20879 | 4142/20724 | 1381/6907 | chr2 | 185791278 | ||
| chr2:185792126
|
G | A | 1 | a0057 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.4990G>A | p.Asp1664Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5081/20879 | 4990/20724 | 1664/6907 | chr2 | 185792126 | ||
| chr2:185792162
|
A | T | 3 | a0016a0018a0029 | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
missense_variant | MODERATE | c.5026A>T | p.Thr1676Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5117/20879 | 5026/20724 | 1676/6907 | chr2 | 185792162 | ||
| chr2:185792229
|
T | C | 34 | a0002a0003a0005others(31): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.5093T>C | p.Met1698Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5184/20879 | 5093/20724 | 1698/6907 | chr2 | 185792229 | ||
| chr2:185792230
|
G | A | 1 | a0024 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.5094G>A | p.Met1698Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5185/20879 | 5094/20724 | 1698/6907 | chr2 | 185792230 | ||
| chr2:185792307
|
A | G | 1 | a0040 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.5171A>G | p.Asp1724Gly | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5262/20879 | 5171/20724 | 1724/6907 | chr2 | 185792307 | ||
| chr2:185792384
|
A | T | 1 | a0043 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.5248A>T | p.Thr1750Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5339/20879 | 5248/20724 | 1750/6907 | chr2 | 185792384 | ||
| chr2:185792658
|
T | C | 1 | a0026 | 2 | HG02109.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.5522T>C | p.Ile1841Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5613/20879 | 5522/20724 | 1841/6907 | chr2 | 185792658 | ||
| chr2:185792966
|
G | C | 1 | a0032 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.5830G>C | p.Val1944Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5921/20879 | 5830/20724 | 1944/6907 | chr2 | 185792966 | ||
| chr2:185793026
|
G | A | 1 | a0028 | 2 | NA18961.hp2 NA19070.hp2 |
missense_variant | MODERATE | c.5890G>A | p.Ala1964Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5981/20879 | 5890/20724 | 1964/6907 | chr2 | 185793026 | ||
| chr2:185793329
|
G | A | 33 | a0002a0003a0005others(30): Show | 189 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
missense_variant | MODERATE | c.6193G>A | p.Asp2065Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 6284/20879 | 6193/20724 | 2065/6907 | chr2 | 185793329 | ||
| chr2:185793330
|
A | G | 1 | a0060 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.6194A>G | p.Asp2065Gly | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 6285/20879 | 6194/20724 | 2065/6907 | chr2 | 185793330 | ||
| chr2:185793362
|
C | A | 1 | a0050 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.6226C>A | p.Leu2076Met | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 6317/20879 | 6226/20724 | 2076/6907 | chr2 | 185793362 | ||
| chr2:185793711
|
C | T | 34 | a0002a0003a0005others(31): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.6575C>T | p.Thr2192Met | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 6666/20879 | 6575/20724 | 2192/6907 | chr2 | 185793711 | ||
| chr2:185793838
|
G | T | 34 | a0002a0003a0005others(31): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.6702G>T | p.Glu2234Asp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 6793/20879 | 6702/20724 | 2234/6907 | chr2 | 185793838 | ||
| chr2:185794059
|
A | T | 3 | a0016a0018a0029 | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
missense_variant | MODERATE | c.6923A>T | p.Asp2308Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7014/20879 | 6923/20724 | 2308/6907 | chr2 | 185794059 | ||
| chr2:185794125
|
T | C | 1 | a0039 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.6989T>C | p.Phe2330Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7080/20879 | 6989/20724 | 2330/6907 | chr2 | 185794125 | ||
| chr2:185794457
|
C | A | 1 | a0010 | 7 | HG00099.hp2 HG00741.hp1 HG01106.hp2 others(4): Show |
missense_variant | MODERATE | c.7321C>A | p.Gln2441Lys | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7412/20879 | 7321/20724 | 2441/6907 | chr2 | 185794457 | ||
| chr2:185794632
|
G | T | 34 | a0002a0003a0005others(31): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.7496G>T | p.Arg2499Met | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7587/20879 | 7496/20724 | 2499/6907 | chr2 | 185794632 | ||
| chr2:185795244
|
A | G | 1 | a0038 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.8108A>G | p.Lys2703Arg | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 8199/20879 | 8108/20724 | 2703/6907 | chr2 | 185795244 | ||
| chr2:185795285
|
A | G | 1 | a0014 | 5 | HG02257.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.8149A>G | p.Met2717Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 8240/20879 | 8149/20724 | 2717/6907 | chr2 | 185795285 | ||
| chr2:185795834
|
A | G | 1 | a0045 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.8698A>G | p.Lys2900Glu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 8789/20879 | 8698/20724 | 2900/6907 | chr2 | 185795834 | ||
| chr2:185796014
|
T | C | 3 | a0016a0018a0029 | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
missense_variant | MODERATE | c.8878T>C | p.Phe2960Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 8969/20879 | 8878/20724 | 2960/6907 | chr2 | 185796014 | ||
| chr2:185796038
|
A | G | 1 | a0011 | 5 | NA18944.hp1 NA18972.hp2 NA18989.hp1 others(2): Show |
missense_variant | MODERATE | c.8902A>G | p.Ser2968Gly | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 8993/20879 | 8902/20724 | 2968/6907 | chr2 | 185796038 | ||
| chr2:185796296
|
G | A | 1 | a0037 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.9160G>A | p.Glu3054Lys | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9251/20879 | 9160/20724 | 3054/6907 | chr2 | 185796296 | ||
| chr2:185796449
|
G | C | 2 | a0006a0049 | 15 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
missense_variant | MODERATE | c.9313G>C | p.Glu3105Gln | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9404/20879 | 9313/20724 | 3105/6907 | chr2 | 185796449 | ||
| chr2:185796672
|
A | G | 1 | a0050 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.9536A>G | p.Asn3179Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9627/20879 | 9536/20724 | 3179/6907 | chr2 | 185796672 | ||
| chr2:185796840
|
G | A | 2 | a0013a0036 | 6 | HG01109.hp2 HG01168.hp2 HG01175.hp2 others(3): Show |
missense_variant | MODERATE | c.9704G>A | p.Cys3235Tyr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9795/20879 | 9704/20724 | 3235/6907 | chr2 | 185796840 | ||
| chr2:185800098
|
G | A | 1 | a0009 | 8 | HG01167.hp2 HG01169.hp2 HG01928.hp1 others(5): Show |
missense_variant | MODERATE | c.10792G>A | p.Gly3598Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 10883/20879 | 10792/20724 | 3598/6907 | chr2 | 185800098 | ||
| chr2:185800171
|
A | G | 1 | a0037 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.10865A>G | p.Asp3622Gly | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 10956/20879 | 10865/20724 | 3622/6907 | chr2 | 185800171 | ||
| chr2:185800236
|
C | A | 34 | a0002a0003a0005others(31): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.10930C>A | p.Leu3644Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11021/20879 | 10930/20724 | 3644/6907 | chr2 | 185800236 | ||
| chr2:185800371
|
A | G | 2 | a0022a0033 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.11065A>G | p.Thr3689Ala | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11156/20879 | 11065/20724 | 3689/6907 | chr2 | 185800371 | ||
| chr2:185800464
|
G | C | 3 | a0016a0018a0029 | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
missense_variant | MODERATE | c.11158G>C | p.Gly3720Arg | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11249/20879 | 11158/20724 | 3720/6907 | chr2 | 185800464 | ||
| chr2:185800525
|
C | A | 1 | a0046 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.11219C>A | p.Thr3740Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11310/20879 | 11219/20724 | 3740/6907 | chr2 | 185800525 | ||
| chr2:185800705
|
G | A | 34 | a0002a0003a0005others(31): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.11399G>A | p.Gly3800Glu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11490/20879 | 11399/20724 | 3800/6907 | chr2 | 185800705 | ||
| chr2:185800903
|
T | C | 1 | a0035 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.11597T>C | p.Leu3866Pro | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11688/20879 | 11597/20724 | 3866/6907 | chr2 | 185800903 | ||
| chr2:185801097
|
A | G | 34 | a0002a0003a0005others(31): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.11791A>G | p.Asn3931Asp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 11882/20879 | 11791/20724 | 3931/6907 | chr2 | 185801097 | ||
| chr2:185801616
|
T | A | 1 | a0025 | 2 | HG03130.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.12310T>A | p.Ser4104Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 12401/20879 | 12310/20724 | 4104/6907 | chr2 | 185801616 | ||
| chr2:185801624
|
C | G | 1 | a0049 | 1 | HG02055.hp2 | stop_gained | HIGH | c.12318C>G | p.Tyr4106* | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 12409/20879 | 12318/20724 | 4106/6907 | chr2 | 185801624 | ||
| chr2:185802394
|
T | C | 34 | a0002a0003a0005others(31): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.13088T>C | p.Phe4363Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 13179/20879 | 13088/20724 | 4363/6907 | chr2 | 185802394 | ||
| chr2:185802633
|
A | C | 7 | a0004a0020a0022others(4): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
missense_variant | MODERATE | c.13327A>C | p.Ile4443Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 13418/20879 | 13327/20724 | 4443/6907 | chr2 | 185802633 | ||
| chr2:185802924
|
A | G | 1 | a0048 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.13618A>G | p.Ile4540Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 13709/20879 | 13618/20724 | 4540/6907 | chr2 | 185802924 | ||
| chr2:185803293
|
C | T | 1 | a0018 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.13987C>T | p.His4663Tyr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14078/20879 | 13987/20724 | 4663/6907 | chr2 | 185803293 | ||
| chr2:185803357
|
T | C | 1 | a0035 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.14051T>C | p.Leu4684Pro | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14142/20879 | 14051/20724 | 4684/6907 | chr2 | 185803357 | ||
| chr2:185803399
|
T | C | 1 | a0057 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.14093T>C | p.Val4698Ala | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14184/20879 | 14093/20724 | 4698/6907 | chr2 | 185803399 | ||
| chr2:185803494
|
A | C | 2 | a0016a0018 | 9 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
missense_variant | MODERATE | c.14188A>C | p.Ile4730Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14279/20879 | 14188/20724 | 4730/6907 | chr2 | 185803494 | ||
| chr2:185803987
|
A | T | 1 | a0017 | 5 | HG00280.hp1 HG00323.hp2 HG03491.hp2 others(2): Show |
missense_variant | MODERATE | c.14681A>T | p.Lys4894Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14772/20879 | 14681/20724 | 4894/6907 | chr2 | 185803987 | ||
| chr2:185804208
|
A | G | 17 | a0001a0008a0010others(14): Show | 115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
missense_variant | MODERATE | c.14902A>G | p.Met4968Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14993/20879 | 14902/20724 | 4968/6907 | chr2 | 185804208 | ||
| chr2:185804321
|
T | A | 1 | a0022 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.15015T>A | p.Asp5005Glu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15106/20879 | 15015/20724 | 5005/6907 | chr2 | 185804321 | ||
| chr2:185804469
|
A | G | 1 | a0047 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.15163A>G | p.Arg5055Gly | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15254/20879 | 15163/20724 | 5055/6907 | chr2 | 185804469 | ||
| chr2:185804545
|
C | A | 1 | a0036 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.15239C>A | p.Ser5080Tyr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15330/20879 | 15239/20724 | 5080/6907 | chr2 | 185804545 | ||
| chr2:185804598
|
A | G | 1 | a0056 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.15292A>G | p.Ile5098Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15383/20879 | 15292/20724 | 5098/6907 | chr2 | 185804598 | ||
| chr2:185804813
|
G | T | 2 | a0052a0058 | 2 | NA18955.hp1 NA19007.hp2 |
missense_variant | MODERATE | c.15507G>T | p.Glu5169Asp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15598/20879 | 15507/20724 | 5169/6907 | chr2 | 185804813 | ||
| chr2:185805177
|
C | T | 1 | a0053 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.15871C>T | p.Leu5291Phe | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15962/20879 | 15871/20724 | 5291/6907 | chr2 | 185805177 | ||
| chr2:185805377
|
A | C | 58 | a0001a0002a0003others(55): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
missense_variant | MODERATE | c.16071A>C | p.Glu5357Asp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 16162/20879 | 16071/20724 | 5357/6907 | chr2 | 185805377 | ||
| chr2:185805652
|
C | T | 1 | a0012 | 5 | HG01261.hp1 NA18948.hp1 NA18986.hp2 others(2): Show |
missense_variant | MODERATE | c.16346C>T | p.Thr5449Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 16437/20879 | 16346/20724 | 5449/6907 | chr2 | 185805652 | ||
| chr2:185806053
|
T | A | 30 | a0002a0003a0005others(27): Show | 179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
missense_variant | MODERATE | c.16747T>A | p.Tyr5583Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 16838/20879 | 16747/20724 | 5583/6907 | chr2 | 185806053 | ||
| chr2:185806252
|
T | C | 51 | a0001a0002a0003others(48): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
missense_variant | MODERATE | c.16946T>C | p.Ile5649Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17037/20879 | 16946/20724 | 5649/6907 | chr2 | 185806252 | ||
| chr2:185806387
|
C | T | 4 | a0016a0018a0029others(1): Show | 11 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(8): Show |
missense_variant | MODERATE | c.17081C>T | p.Ser5694Phe | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17172/20879 | 17081/20724 | 5694/6907 | chr2 | 185806387 | ||
| chr2:185806504
|
A | T | 1 | a0029 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.17198A>T | p.Lys5733Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17289/20879 | 17198/20724 | 5733/6907 | chr2 | 185806504 | ||
| chr2:185806630
|
G | A | 34 | a0002a0003a0005others(31): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.17324G>A | p.Arg5775Gln | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17415/20879 | 17324/20724 | 5775/6907 | chr2 | 185806630 | ||
| chr2:185807004
|
C | A | 1 | a0035 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.17698C>A | p.Pro5900Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17789/20879 | 17698/20724 | 5900/6907 | chr2 | 185807004 | ||
| chr2:185807185
|
G | A | 34 | a0002a0003a0005others(31): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
missense_variant | MODERATE | c.17879G>A | p.Arg5960His | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17970/20879 | 17879/20724 | 5960/6907 | chr2 | 185807185 | ||
| chr2:185807596
|
G | T | 1 | a0034 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.18290G>T | p.Gly6097Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 18381/20879 | 18290/20724 | 6097/6907 | chr2 | 185807596 | ||
| chr2:185807800
|
T | A | 8 | a0005a0009a0023others(5): Show | 42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
missense_variant | MODERATE | c.18494T>A | p.Leu6165Gln | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 18585/20879 | 18494/20724 | 6165/6907 | chr2 | 185807800 | ||
| chr2:185808588
|
A | C | 1 | a0027 | 2 | HG00639.hp2 HG01167.hp1 |
missense_variant | MODERATE | c.19282A>C | p.Asn6428His | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 19373/20879 | 19282/20724 | 6428/6907 | chr2 | 185808588 | ||
| chr2:185808891
|
C | A | 2 | a0019a0024 | 7 | HG00544.hp2 HG00597.hp2 HG02071.hp2 others(4): Show |
missense_variant | MODERATE | c.19585C>A | p.Pro6529Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 19676/20879 | 19585/20724 | 6529/6907 | chr2 | 185808891 | ||
| chr2:185808901
|
T | C | 1 | a0020 | 4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.19595T>C | p.Ile6532Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 19686/20879 | 19595/20724 | 6532/6907 | chr2 | 185808901 | ||
| chr2:185809103
|
G | C | 1 | a0054 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.19797G>C | p.Lys6599Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 19888/20879 | 19797/20724 | 6599/6907 | chr2 | 185809103 | ||
| chr2:185813906
|
C | T | 2 | a0008a0021 | 13 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
missense_variant | MODERATE | c.20189C>T | p.Thr6730Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/23 | 20280/20879 | 20189/20724 | 6730/6907 | chr2 | 185813906 | ||
| chr2:185833149
|
A | G | 58 | a0001a0002a0003others(55): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
missense_variant | MODERATE | c.20647A>G | p.Thr6883Ala | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 23/23 | 20738/20879 | 20647/20724 | 6883/6907 | chr2 | 185833149 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:185739456
|
G | C | 1 | a0033c0035 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.210G>C | p.Thr70Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/23 | 301/20879 | 210/20724 | 70/6907 | chr2 | 185739456 | ||
| chr2:185743162
|
G | C | 1 | a0043c0036 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.255G>C | p.Leu85Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/23 | 346/20879 | 255/20724 | 85/6907 | chr2 | 185743162 | ||
| chr2:185743184
|
T | C | 1 | a0020c0020 | 4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
synonymous_variant | LOW | c.277T>C | p.Leu93Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/23 | 368/20879 | 277/20724 | 93/6907 | chr2 | 185743184 | ||
| chr2:185746768
|
A | G | 1 | a0003c0081 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.717A>G | p.Glu239Glu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 6/23 | 808/20879 | 717/20724 | 239/6907 | chr2 | 185746768 | ||
| chr2:185761040
|
G | A | 4 | a0016c0022a0016c0038a0018c0021others(1): Show | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
synonymous_variant | LOW | c.1131G>A | p.Thr377Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/23 | 1222/20879 | 1131/20724 | 377/6907 | chr2 | 185761040 | ||
| chr2:185761043
|
A | G | 46 | a0002c0002a0002c0018a0002c0057others(43): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
synonymous_variant | LOW | c.1134A>G | p.Lys378Lys | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/23 | 1225/20879 | 1134/20724 | 378/6907 | chr2 | 185761043 | ||
| chr2:185788819
|
G | A | 8 | a0004c0004a0004c0041a0020c0020others(5): Show | 38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
synonymous_variant | LOW | c.1683G>A | p.Thr561Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 1774/20879 | 1683/20724 | 561/6907 | chr2 | 185788819 | ||
| chr2:185789227
|
A | G | 1 | a0061c0037 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.2091A>G | p.Lys697Lys | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 2182/20879 | 2091/20724 | 697/6907 | chr2 | 185789227 | ||
| chr2:185789273
|
C | A | 1 | a0001c0043 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.2137C>A | p.Arg713Arg | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 2228/20879 | 2137/20724 | 713/6907 | chr2 | 185789273 | ||
| chr2:185791930
|
C | T | 55 | a0002c0002a0002c0018a0002c0057others(52): Show | 230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
synonymous_variant | LOW | c.4794C>T | p.Asn1598Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 4885/20879 | 4794/20724 | 1598/6907 | chr2 | 185791930 | ||
| chr2:185792113
|
T | C | 8 | a0003c0066a0005c0005a0009c0009others(5): Show | 42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
synonymous_variant | LOW | c.4977T>C | p.Asn1659Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5068/20879 | 4977/20724 | 1659/6907 | chr2 | 185792113 | ||
| chr2:185792362
|
C | A | 46 | a0002c0002a0002c0018a0002c0057others(43): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
synonymous_variant | LOW | c.5226C>A | p.Ser1742Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 5317/20879 | 5226/20724 | 1742/6907 | chr2 | 185792362 | ||
| chr2:185794186
|
A | G | 1 | a0003c0076 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.7050A>G | p.Thr2350Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7141/20879 | 7050/20724 | 2350/6907 | chr2 | 185794186 | ||
| chr2:185794387
|
T | A | 1 | a0016c0038 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.7251T>A | p.Ser2417Ser | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7342/20879 | 7251/20724 | 2417/6907 | chr2 | 185794387 | ||
| chr2:185794502
|
T | C | 1 | a0001c0008 | 8 | HG02080.hp2 HG02083.hp2 HG02523.hp2 others(5): Show |
synonymous_variant | LOW | c.7366T>C | p.Leu2456Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7457/20879 | 7366/20724 | 2456/6907 | chr2 | 185794502 | ||
| chr2:185794675
|
C | T | 1 | a0002c0062 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.7539C>T | p.Asn2513Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 7630/20879 | 7539/20724 | 2513/6907 | chr2 | 185794675 | ||
| chr2:185796152
|
T | C | 1 | a0004c0041 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.9016T>C | p.Leu3006Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9107/20879 | 9016/20724 | 3006/6907 | chr2 | 185796152 | ||
| chr2:185796346
|
G | C | 1 | a0035c0042 | 1 | NA18989.hp2 | synonymous_variant | LOW | c.9210G>C | p.Arg3070Arg | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9301/20879 | 9210/20724 | 3070/6907 | chr2 | 185796346 | ||
| chr2:185796946
|
A | G | 46 | a0002c0002a0002c0018a0002c0057others(43): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
synonymous_variant | LOW | c.9810A>G | p.Leu3270Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 9901/20879 | 9810/20724 | 3270/6907 | chr2 | 185796946 | ||
| chr2:185797189
|
G | A | 1 | a0060c0079 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.10053G>A | p.Glu3351Glu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 10144/20879 | 10053/20724 | 3351/6907 | chr2 | 185797189 | ||
| chr2:185797348
|
G | A | 2 | a0020c0020a0062c0080 | 5 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
synonymous_variant | LOW | c.10212G>A | p.Arg3404Arg | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 10303/20879 | 10212/20724 | 3404/6907 | chr2 | 185797348 | ||
| chr2:185797369
|
A | G | 2 | a0003c0012a0003c0075 | 7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
synonymous_variant | LOW | c.10233A>G | p.Gln3411Gln | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/23 | 10324/20879 | 10233/20724 | 3411/6907 | chr2 | 185797369 | ||
| chr2:185799746
|
T | C | 46 | a0002c0002a0002c0018a0002c0057others(43): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
synonymous_variant | LOW | c.10440T>C | p.Tyr3480Tyr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 10531/20879 | 10440/20724 | 3480/6907 | chr2 | 185799746 | ||
| chr2:185801525
|
C | T | 1 | a0001c0023 | 4 | NA18981.hp2 NA18998.hp1 NA19003.hp1 others(1): Show |
synonymous_variant | LOW | c.12219C>T | p.Ala4073Ala | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 12310/20879 | 12219/20724 | 4073/6907 | chr2 | 185801525 | ||
| chr2:185801687
|
A | C | 1 | a0023c0028 | 3 | HG02145.hp1 HG02976.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.12381A>C | p.Leu4127Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 12472/20879 | 12381/20724 | 4127/6907 | chr2 | 185801687 | ||
| chr2:185801708
|
T | C | 2 | a0003c0072a0048c0073 | 2 | HG02647.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.12402T>C | p.Tyr4134Tyr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 12493/20879 | 12402/20724 | 4134/6907 | chr2 | 185801708 | ||
| chr2:185801786
|
A | G | 1 | a0006c0069 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.12480A>G | p.Thr4160Thr | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 12571/20879 | 12480/20724 | 4160/6907 | chr2 | 185801786 | ||
| chr2:185803196
|
T | G | 1 | a0003c0075 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.13890T>G | p.Val4630Val | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 13981/20879 | 13890/20724 | 4630/6907 | chr2 | 185803196 | ||
| chr2:185804189
|
T | G | 1 | a0010c0047 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.14883T>G | p.Leu4961Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 14974/20879 | 14883/20724 | 4961/6907 | chr2 | 185804189 | ||
| chr2:185804585
|
A | G | 1 | a0001c0051 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.15279A>G | p.Arg5093Arg | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15370/20879 | 15279/20724 | 5093/6907 | chr2 | 185804585 | ||
| chr2:185804999
|
C | A | 1 | a0018c0021 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.15693C>A | p.Ile5231Ile | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 15784/20879 | 15693/20724 | 5231/6907 | chr2 | 185804999 | ||
| chr2:185806529
|
T | C | 1 | a0008c0027 | 3 | HG03490.hp2 HG03492.hp2 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.17223T>C | p.Asn5741Asn | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 17314/20879 | 17223/20724 | 5741/6907 | chr2 | 185806529 | ||
| chr2:185808170
|
A | G | 23 | a0001c0001a0001c0008a0001c0023others(20): Show | 115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
synonymous_variant | LOW | c.18864A>G | p.Leu6288Leu | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 18955/20879 | 18864/20724 | 6288/6907 | chr2 | 185808170 | ||
| chr2:185808479
|
T | G | 1 | a0002c0057 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.19173T>G | p.Ala6391Ala | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 19264/20879 | 19173/20724 | 6391/6907 | chr2 | 185808479 | ||
| chr2:185808758
|
C | T | 1 | a0029c0039 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.19452C>T | p.Asp6484Asp | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/23 | 19543/20879 | 19452/20724 | 6484/6907 | chr2 | 185808758 | ||
| chr2:185814030
|
G | A | 1 | a0002c0018 | 5 | NA18981.hp1 NA18984.hp2 NA18999.hp2 others(2): Show |
synonymous_variant | LOW | c.20313G>A | p.Lys6771Lys | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/23 | 20404/20879 | 20313/20724 | 6771/6907 | chr2 | 185814030 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:185738855
|
C | A | 1 | a0004c0004t0004 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-40C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 1/23 | 40 | chr2 | 185738855 | |||||
| chr2:185738878
|
A | AG | 26 | a0001c0001t0002a0001c0008t0002a0001c0023t0002others(23): Show | 127 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(124): Show |
5_prime_UTR_variant | MODIFIER | c.-12dupG | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 1/23 | 11 | INFO_REALIGN_3_PRIME | chr2 | 185738878 | ||||
| chr2:185738891
|
G | A | 3 | a0003c0012t0003a0020c0020t0003a0062c0080t0003 | 7 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-4G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 1/23 | 4 | chr2 | 185738891 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:185739096
|
C | T | 1 | a0027c0033t0001g0311 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99+103C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 1/22 | chr2 | 185739096 | ||||||
| chr2:185739132
|
G | A | 1 | a0024c0034t0001g0037 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.99+139G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 1/22 | chr2 | 185739132 | ||||||
| chr2:185739232
|
G | C | 3 | a0003c0012t0003g0039a0003c0012t0003g0040a0062c0080t0003g0038 | 3 | HG02647.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.100-114G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 1/22 | chr2 | 185739232 | ||||||
| chr2:185739537
|
G | A | 1 | a0055c0056t0001g0041 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.225+66G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185739537 | ||||||
| chr2:185739644
|
C | T | 2 | a0003c0012t0003g0039a0003c0012t0003g0040 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.225+173C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185739644 | ||||||
| chr2:185739764
|
A | T | 262 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(259): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.225+293A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185739764 | ||||||
| chr2:185740123
|
T | C | 110 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(107): Show | 127 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.225+652T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740123 | ||||||
| chr2:185740230
|
G | A | 12 | a0001c0001t0002g0089a0008c0010t0002g0088a0008c0010t0002g0091others(9): Show | 13 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.225+759G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740230 | ||||||
| chr2:185740237
|
C | A | 1 | a0003c0072t0001g0184 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.225+766C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740237 | ||||||
| chr2:185740372
|
C | A | 1 | a0002c0002t0001g0185 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.225+901C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740372 | ||||||
| chr2:185740380
|
C | T | 137 | a0002c0002t0001g0001a0002c0002t0001g0009a0002c0002t0001g0010others(134): Show | 162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.225+909C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740380 | ||||||
| chr2:185740406
|
G | A | 110 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(107): Show | 126 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.225+935G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740406 | ||||||
| chr2:185740680
|
C | T | 1 | a0025c0030t0002g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.225+1209C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740680 | ||||||
| chr2:185740803
|
A | C | 3 | a0003c0003t0001g0308a0003c0003t0001g0309a0003c0003t0001g0310 | 3 | HG01123.hp1 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.225+1332A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740803 | ||||||
| chr2:185740953
|
G | GA | 105 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(102): Show | 121 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.225+1489dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr2 | 185740953 | |||||
| chr2:185740983
|
A | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.225+1512A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185740983 | ||||||
| chr2:185741157
|
C | G | 2 | a0002c0002t0001g0036a0055c0056t0001g0041 | 3 | HG00733.hp2 HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.225+1686C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741157 | ||||||
| chr2:185741198
|
G | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.225+1727G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741198 | ||||||
| chr2:185741284
|
A | AT | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.225+1813_225+1814i others(3): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741284 | ||||||
| chr2:185741291
|
T | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.225+1820T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741291 | ||||||
| chr2:185741299
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.225+1828T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741299 | ||||||
| chr2:185741399
|
G | T | 1 | a0039c0046t0002g0176 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.226-1734G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741399 | ||||||
| chr2:185741688
|
T | C | 1 | a0003c0003t0001g0199 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.226-1445T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741688 | ||||||
| chr2:185741700
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.226-1433G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741700 | ||||||
| chr2:185741707
|
G | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.226-1426G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741707 | ||||||
| chr2:185741762
|
A | G | 1 | a0001c0001t0002g0020 | 2 | NA19004.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.226-1371A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185741762 | ||||||
| chr2:185742063
|
C | G | 1 | a0001c0001t0002g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.226-1070C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185742063 | ||||||
| chr2:185742153
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.226-980C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185742153 | ||||||
| chr2:185742474
|
A | G | 9 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(6): Show | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-659A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185742474 | ||||||
| chr2:185742768
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.226-365T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185742768 | ||||||
| chr2:185742791
|
ATG | A | 9 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(6): Show | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-341_226-340del others(2): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185742791 | ||||||
| chr2:185742792
|
T | A | 154 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(151): Show | 180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.226-341T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185742792 | ||||||
| chr2:185743053
|
A | G | 1 | a0003c0012t0001g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.226-80A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 2/22 | chr2 | 185743053 | ||||||
| chr2:185743612
|
G | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.387+318G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185743612 | ||||||
| chr2:185743654
|
T | C | 1 | a0002c0002t0001g0200 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.387+360T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185743654 | ||||||
| chr2:185743796
|
C | T | 22 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(19): Show | 25 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.387+502C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185743796 | ||||||
| chr2:185743811
|
G | A | 1 | a0004c0004t0001g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.388-511G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185743811 | ||||||
| chr2:185743818
|
G | T | 2 | a0005c0005t0001g0035a0005c0005t0001g0307 | 3 | HG02698.hp1 HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.388-504G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185743818 | ||||||
| chr2:185743987
|
T | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.388-335T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185743987 | ||||||
| chr2:185744022
|
G | A | 1 | a0005c0005t0001g0201 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.388-300G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 3/22 | chr2 | 185744022 | ||||||
| chr2:185744528
|
A | G | 1 | a0004c0041t0001g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.477+117A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185744528 | ||||||
| chr2:185744705
|
C | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.477+294C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185744705 | ||||||
| chr2:185744773
|
C | A | 1 | a0010c0011t0002g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.477+362C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185744773 | ||||||
| chr2:185744868
|
T | C | 3 | a0022c0025t0001g0022a0022c0025t0001g0188a0033c0035t0001g0042 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+457T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185744868 | ||||||
| chr2:185744900
|
A | T | 1 | a0015c0015t0001g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.477+489A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185744900 | ||||||
| chr2:185744963
|
GGTGTGTG others(10): Show |
G | 34 | a0003c0066t0001g0288a0005c0005t0001g0011a0005c0005t0001g0032others(31): Show | 42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.478-452_478-436del others(17): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 185744963 | |||||
| chr2:185744978
|
GGT | G | 161 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(158): Show | 186 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.478-432_478-431del others(2): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 185744978 | |||||
| chr2:185745052
|
A | G | 1 | a0057c0055t0001g0280 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.478-377A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185745052 | ||||||
| chr2:185745139
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.478-290T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185745139 | ||||||
| chr2:185745263
|
A | G | 1 | a0004c0004t0001g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.478-166A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185745263 | ||||||
| chr2:185745306
|
A | C | 19 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0269others(16): Show | 21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.478-123A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185745306 | ||||||
| chr2:185745350
|
A | G | 2 | a0001c0001t0002g0018a0034c0050t0002g0018 | 2 | HG01081.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.478-79A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 4/22 | chr2 | 185745350 | ||||||
| chr2:185745617
|
T | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.617+49T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185745617 | ||||||
| chr2:185745661
|
G | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.617+93G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185745661 | ||||||
| chr2:185745785
|
A | G | 1 | a0001c0001t0002g0172 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.617+217A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185745785 | ||||||
| chr2:185745848
|
T | C | 3 | a0003c0012t0001g0190a0003c0012t0001g0195a0003c0075t0001g0189 | 3 | HG02970.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.617+280T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185745848 | ||||||
| chr2:185745858
|
G | A | 195 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(192): Show | 228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.617+290G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185745858 | ||||||
| chr2:185745985
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.617+417A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185745985 | ||||||
| chr2:185746100
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.617+532A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185746100 | ||||||
| chr2:185746284
|
G | T | 4 | a0006c0006t0001g0276a0006c0006t0001g0277a0006c0006t0001g0278others(1): Show | 4 | HG02280.hp1 HG02615.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-385G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185746284 | ||||||
| chr2:185746288
|
GT | G | 162 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(159): Show | 189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.618-370delT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 185746288 | |||||
| chr2:185746539
|
A | C | 1 | a0009c0009t0001g0306 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.618-130A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 5/22 | chr2 | 185746539 | ||||||
| chr2:185746839
|
C | A | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.759+29C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 6/22 | chr2 | 185746839 | ||||||
| chr2:185747001
|
C | T | 9 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(6): Show | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.759+191C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 6/22 | chr2 | 185747001 | ||||||
| chr2:185747107
|
A | G | 102 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(99): Show | 117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.760-206A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 6/22 | chr2 | 185747107 | ||||||
| chr2:185747211
|
G | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-102G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 6/22 | chr2 | 185747211 | ||||||
| chr2:185747434
|
C | G | 55 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(52): Show | 68 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.870+11C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747434 | ||||||
| chr2:185747467
|
G | T | 1 | a0005c0005t0001g0305 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.870+44G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747467 | ||||||
| chr2:185747668
|
T | C | 1 | a0004c0004t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.870+245T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747668 | ||||||
| chr2:185747707
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.870+284T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747707 | ||||||
| chr2:185747731
|
A | C | 1 | a0005c0005t0001g0304 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.870+308A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747731 | ||||||
| chr2:185747785
|
T | C | 19 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0269others(16): Show | 21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.870+362T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747785 | ||||||
| chr2:185747875
|
A | G | 1 | a0026c0029t0002g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.870+452A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185747875 | ||||||
| chr2:185748210
|
G | A | 3 | a0003c0012t0001g0190a0003c0012t0001g0195a0003c0075t0001g0189 | 3 | HG02970.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.870+787G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185748210 | ||||||
| chr2:185748729
|
G | A | 1 | a0026c0029t0002g0100 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.870+1306G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185748729 | ||||||
| chr2:185748824
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.870+1401T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185748824 | ||||||
| chr2:185748844
|
T | C | 5 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+1421T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185748844 | ||||||
| chr2:185748862
|
A | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.870+1439A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185748862 | ||||||
| chr2:185748905
|
T | C | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.870+1482T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185748905 | ||||||
| chr2:185749020
|
C | T | 1 | a0003c0003t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.870+1597C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185749020 | ||||||
| chr2:185749156
|
G | A | 99 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(96): Show | 114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.870+1733G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185749156 | ||||||
| chr2:185749205
|
TG | T | 10 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(7): Show | 11 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.870+1784delG | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185749205 | |||||
| chr2:185749335
|
T | C | 34 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(31): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.870+1912T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185749335 | ||||||
| chr2:185749356
|
C | T | 62 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(59): Show | 76 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.870+1933C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185749356 | ||||||
| chr2:185749734
|
G | T | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.870+2311G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185749734 | ||||||
| chr2:185749793
|
G | A | 3 | a0020c0020t0003g0013a0020c0020t0003g0062a0020c0020t0003g0063 | 4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2370G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185749793 | ||||||
| chr2:185750155
|
G | T | 7 | a0003c0012t0001g0190a0003c0012t0001g0192a0003c0012t0001g0193others(4): Show | 7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.870+2732G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185750155 | ||||||
| chr2:185750227
|
G | A | 93 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(90): Show | 109 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.870+2804G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185750227 | ||||||
| chr2:185750519
|
C | A | 1 | a0017c0019t0001g0202 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.870+3096C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185750519 | ||||||
| chr2:185750603
|
G | GT | 270 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(267): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.871-3107dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185750603 | |||||
| chr2:185750646
|
T | C | 1 | a0003c0003t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.871-3076T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185750646 | ||||||
| chr2:185750936
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.871-2786A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185750936 | ||||||
| chr2:185751194
|
G | C | 30 | a0003c0066t0001g0288a0005c0005t0001g0011a0005c0005t0001g0032others(27): Show | 37 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.871-2528G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751194 | ||||||
| chr2:185751217
|
G | A | 1 | a0002c0062t0001g0231 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.871-2505G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751217 | ||||||
| chr2:185751423
|
T | C | 2 | a0002c0002t0001g0036a0055c0056t0001g0041 | 3 | HG00733.hp2 HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.871-2299T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751423 | ||||||
| chr2:185751439
|
C | T | 3 | a0018c0021t0001g0023a0018c0021t0001g0197a0018c0021t0001g0198 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-2283C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751439 | ||||||
| chr2:185751461
|
C | CTCTG | 5 | a0003c0012t0001g0190a0003c0012t0001g0192a0003c0012t0003g0039others(2): Show | 5 | HG02818.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-2260_871-2259i others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | |||||
| chr2:185751461
|
C | CTCTGTGT others(3): Show |
1 | a0001c0001t0002g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.871-2260_871-2259i others(12): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | |||||
| chr2:185751461
|
C | CTG | 34 | a0001c0001t0002g0016a0002c0002t0001g0026a0003c0003t0001g0205others(31): Show | 38 | HG00423.hp2 HG01346.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.871-2224_871-2223d others(4): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | |||||
| chr2:185751461
|
C | CTGTG | 81 | a0002c0002t0001g0001a0002c0002t0001g0009a0002c0002t0001g0010others(78): Show | 97 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.871-2226_871-2223d others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | |||||
| chr2:185751461
|
C | CTGTGTG | 42 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0118others(39): Show | 47 | HG00423.hp1 HG01071.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.871-2228_871-2223d others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | |||||
| chr2:185751461
|
C | CTGTGTGT others(1): Show |
42 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0020others(39): Show | 50 | HG00099.hp2 HG00597.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.871-2230_871-2223d others(10): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | |||||
| chr2:185751461
|
C | CTGTGTGT others(3): Show |
39 | a0001c0001t0002g0098a0001c0001t0002g0112a0001c0001t0002g0113others(36): Show | 43 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.871-2232_871-2223d others(12): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | |||||
| chr2:185751461
|
C | CTGTGTGT others(5): Show |
7 | a0001c0001t0002g0165a0003c0003t0001g0264a0003c0072t0001g0184others(4): Show | 7 | HG02559.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-2234_871-2223d others(14): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | |||||
| chr2:185751461
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0002g0166 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.871-2238_871-2223d others(18): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | |||||
| chr2:185751461
|
CTG | C | 24 | a0003c0003t0001g0203a0004c0004t0001g0005a0004c0004t0001g0065others(21): Show | 28 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.871-2224_871-2223d others(4): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751461 | |||||
| chr2:185751486
|
T | TGTGTGCG others(1): Show |
29 | a0003c0066t0001g0288a0005c0005t0001g0011a0005c0005t0001g0032others(26): Show | 36 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.871-2231_871-2230i others(10): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751486 | |||||
| chr2:185751486
|
T | TGTGTGTG others(3): Show |
3 | a0005c0005t0001g0300a0023c0028t0001g0034a0023c0028t0001g0302 | 4 | HG01952.hp2 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2229_871-2228i others(12): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751486 | |||||
| chr2:185751524
|
T | C | 2 | a0010c0011t0002g0105a0010c0011t0002g0106 | 2 | HG00099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.871-2198T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751524 | ||||||
| chr2:185751644
|
A | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.871-2078A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751644 | ||||||
| chr2:185751712
|
G | A | 1 | a0004c0004t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.871-2010G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751712 | ||||||
| chr2:185751768
|
CTTTAA | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.871-1949_871-1945d others(7): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751768 | |||||
| chr2:185751849
|
T | C | 3 | a0018c0021t0001g0023a0018c0021t0001g0197a0018c0021t0001g0198 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-1873T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751849 | ||||||
| chr2:185751858
|
A | AT | 93 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(90): Show | 109 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.871-1857dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185751858 | |||||
| chr2:185751937
|
A | T | 13 | a0001c0001t0002g0008a0001c0001t0002g0020a0001c0001t0002g0135others(10): Show | 17 | HG02273.hp1 NA18939.hp2 NA18949.hp1 others(14): Show |
intron_variant | MODIFIER | c.871-1785A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751937 | ||||||
| chr2:185751979
|
TGTA | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.871-1742_871-1740d others(5): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185751979 | ||||||
| chr2:185752067
|
A | AT | 66 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(63): Show | 80 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.871-1646dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185752067 | |||||
| chr2:185752166
|
T | C | 5 | a0003c0003t0001g0025a0003c0003t0001g0199a0003c0003t0001g0205others(2): Show | 6 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.871-1556T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185752166 | ||||||
| chr2:185752200
|
G | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.871-1522G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185752200 | ||||||
| chr2:185752399
|
T | G | 1 | a0012c0016t0001g0059 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.871-1323T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185752399 | ||||||
| chr2:185752639
|
T | C | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.871-1083T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185752639 | ||||||
| chr2:185753072
|
C | T | 1 | a0002c0002t0001g0259 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.871-650C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753072 | ||||||
| chr2:185753108
|
C | A | 32 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(29): Show | 38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.871-614C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753108 | ||||||
| chr2:185753280
|
T | G | 153 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(150): Show | 179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.871-442T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753280 | ||||||
| chr2:185753346
|
A | T | 1 | a0001c0001t0002g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.871-376A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753346 | ||||||
| chr2:185753360
|
G | C | 1 | a0011c0017t0001g0044 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.871-362G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753360 | ||||||
| chr2:185753497
|
C | A | 1 | a0004c0004t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.871-225C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753497 | ||||||
| chr2:185753526
|
A | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.871-196A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753526 | ||||||
| chr2:185753599
|
C | A | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871-123C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | chr2 | 185753599 | ||||||
| chr2:185753643
|
T | TGTCACA | 3 | a0014c0014t0002g0101a0014c0014t0002g0102a0014c0014t0002g0103 | 3 | HG02615.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.871-78_871-73dupGT others(4): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 185753643 | |||||
| chr2:185753929
|
A | G | 1 | a0002c0002t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.991+87A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185753929 | ||||||
| chr2:185753980
|
T | C | 1 | a0001c0001t0002g0016 | 2 | NA18953.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.991+138T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185753980 | ||||||
| chr2:185754163
|
G | A | 1 | a0005c0005t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.991+321G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185754163 | ||||||
| chr2:185754166
|
C | A | 1 | a0005c0005t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.991+324C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185754166 | ||||||
| chr2:185754632
|
T | C | 1 | a0004c0004t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.991+790T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185754632 | ||||||
| chr2:185755061
|
C | T | 9 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(6): Show | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.992-1131C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755061 | ||||||
| chr2:185755152
|
C | G | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.992-1040C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755152 | ||||||
| chr2:185755486
|
G | T | 1 | a0021c0026t0002g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.992-706G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755486 | ||||||
| chr2:185755524
|
A | G | 2 | a0004c0004t0001g0081a0004c0004t0002g0021 | 3 | HG02486.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.992-668A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755524 | ||||||
| chr2:185755765
|
A | G | 2 | a0026c0029t0002g0100a0026c0029t0002g0170 | 2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.992-427A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755765 | ||||||
| chr2:185755890
|
A | G | 1 | a0004c0004t0001g0080 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.992-302A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755890 | ||||||
| chr2:185755967
|
A | T | 1 | a0004c0004t0002g0021 | 2 | HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.992-225A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185755967 | ||||||
| chr2:185756062
|
T | C | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.992-130T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 8/22 | chr2 | 185756062 | ||||||
| chr2:185756340
|
T | A | 10 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(7): Show | 11 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1078+62T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756340 | ||||||
| chr2:185756366
|
G | T | 1 | a0035c0042t0001g0079 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1078+88G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756366 | ||||||
| chr2:185756559
|
T | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1078+281T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756559 | ||||||
| chr2:185756585
|
T | G | 102 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(99): Show | 117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1078+307T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756585 | ||||||
| chr2:185756684
|
A | G | 1 | a0001c0008t0002g0160 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1078+406A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756684 | ||||||
| chr2:185756732
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1078+454T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756732 | ||||||
| chr2:185756837
|
G | A | 65 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(62): Show | 79 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1078+559G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756837 | ||||||
| chr2:185756911
|
T | C | 2 | a0023c0028t0001g0034a0023c0028t0001g0302 | 3 | HG02145.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1078+633T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756911 | ||||||
| chr2:185756995
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1078+717T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185756995 | ||||||
| chr2:185757172
|
C | A | 3 | a0018c0021t0001g0023a0018c0021t0001g0197a0018c0021t0001g0198 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078+894C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185757172 | ||||||
| chr2:185757256
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1078+978C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185757256 | ||||||
| chr2:185757366
|
TA | T | 3 | a0018c0021t0001g0023a0018c0021t0001g0197a0018c0021t0001g0198 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078+1091delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185757366 | |||||
| chr2:185757526
|
A | G | 1 | a0043c0036t0001g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1078+1248A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185757526 | ||||||
| chr2:185757616
|
A | T | 3 | a0022c0025t0001g0022a0022c0025t0001g0188a0033c0035t0001g0042 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078+1338A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185757616 | ||||||
| chr2:185757673
|
G | T | 1 | a0001c0001t0002g0098 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1078+1395G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185757673 | ||||||
| chr2:185757676
|
CCATA | C | 153 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(150): Show | 179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1078+1401_1078+140 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185757676 | |||||
| chr2:185757746
|
T | C | 1 | a0001c0008t0002g0160 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1078+1468T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185757746 | ||||||
| chr2:185758066
|
T | G | 1 | a0010c0011t0002g0107 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1078+1788T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758066 | ||||||
| chr2:185758092
|
T | C | 10 | a0001c0001t0002g0108a0001c0001t0002g0112a0001c0001t0002g0113others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1078+1814T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758092 | ||||||
| chr2:185758156
|
C | T | 1 | a0005c0005t0001g0303 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1078+1878C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758156 | ||||||
| chr2:185758159
|
G | A | 2 | a0013c0013t0002g0121a0036c0049t0002g0122 | 2 | HG01109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1078+1881G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758159 | ||||||
| chr2:185758603
|
T | C | 154 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(151): Show | 182 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1078+2325T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758603 | ||||||
| chr2:185758661
|
T | C | 112 | a0002c0002t0001g0219a0002c0002t0001g0234a0002c0002t0001g0263others(109): Show | 126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1079-2327T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758661 | ||||||
| chr2:185758682
|
T | G | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1079-2306T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758682 | ||||||
| chr2:185758798
|
T | A | 45 | a0002c0002t0001g0001a0002c0002t0001g0009a0002c0002t0001g0010others(42): Show | 57 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1079-2190T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758798 | ||||||
| chr2:185758893
|
G | A | 65 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(62): Show | 79 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1079-2095G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185758893 | ||||||
| chr2:185759016
|
G | T | 1 | a0004c0004t0002g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1079-1972G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185759016 | ||||||
| chr2:185759416
|
ATAT | A | 14 | a0001c0001t0002g0008a0001c0001t0002g0020a0001c0001t0002g0135others(11): Show | 18 | HG02273.hp1 HG03486.hp1 NA18939.hp2 others(15): Show |
intron_variant | MODIFIER | c.1079-1566_1079-156 others(7): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185759416 | |||||
| chr2:185759497
|
T | C | 34 | a0003c0066t0001g0288a0005c0005t0001g0011a0005c0005t0001g0032others(31): Show | 42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1079-1491T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185759497 | ||||||
| chr2:185759600
|
ATAT | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1079-1382_1079-138 others(7): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185759600 | |||||
| chr2:185759801
|
G | C | 1 | a0004c0004t0001g0068 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1079-1187G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185759801 | ||||||
| chr2:185760011
|
CA | C | 146 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(143): Show | 172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1079-976delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760011 | ||||||
| chr2:185760100
|
A | G | 1 | a0009c0009t0001g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1079-888A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760100 | ||||||
| chr2:185760101
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1079-887A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760101 | ||||||
| chr2:185760188
|
TTCTC | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1079-794_1079-791d others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185760188 | |||||
| chr2:185760329
|
T | A | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1079-659T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760329 | ||||||
| chr2:185760408
|
G | GA | 101 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1079-571dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185760408 | |||||
| chr2:185760591
|
T | C | 1 | a0001c0001t0002g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1079-397T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760591 | ||||||
| chr2:185760715
|
C | T | 1 | a0024c0034t0001g0037 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1079-273C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760715 | ||||||
| chr2:185760770
|
T | C | 32 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(29): Show | 38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1079-218T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | chr2 | 185760770 | ||||||
| chr2:185760918
|
TTTGA | T | 101 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1079-66_1079-63del others(4): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185760918 | |||||
| chr2:185760943
|
TA | T | 126 | a0001c0023t0002g0138a0002c0002t0001g0001a0002c0002t0001g0006others(123): Show | 145 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1079-31delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185760943 | |||||
| chr2:185760943
|
TAA | T | 35 | a0003c0066t0001g0288a0005c0005t0001g0011a0005c0005t0001g0032others(32): Show | 43 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1079-32_1079-31del others(2): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 185760943 | |||||
| chr2:185761153
|
C | G | 32 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(29): Show | 38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1194+50C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/22 | chr2 | 185761153 | ||||||
| chr2:185761298
|
A | G | 3 | a0003c0003t0001g0227a0003c0003t0001g0228a0003c0003t0001g0229 | 3 | HG00642.hp2 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1194+195A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/22 | chr2 | 185761298 | ||||||
| chr2:185761425
|
T | C | 1 | a0062c0080t0003g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1194+322T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/22 | chr2 | 185761425 | ||||||
| chr2:185761562
|
T | A | 34 | a0003c0066t0001g0288a0005c0005t0001g0011a0005c0005t0001g0032others(31): Show | 42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1195-410T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/22 | chr2 | 185761562 | ||||||
| chr2:185761827
|
T | C | 2 | a0003c0012t0003g0039a0003c0012t0003g0040 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1195-145T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 10/22 | chr2 | 185761827 | ||||||
| chr2:185762024
|
A | T | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | splice_region_variant&intron_variant | LOW | c.1240+7A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762024 | ||||||
| chr2:185762206
|
G | T | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1240+189G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762206 | ||||||
| chr2:185762289
|
G | C | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1240+272G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762289 | ||||||
| chr2:185762313
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1240+296A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762313 | ||||||
| chr2:185762371
|
A | T | 1 | a0008c0010t0002g0095 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1240+354A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762371 | ||||||
| chr2:185762372
|
C | A | 1 | a0008c0010t0002g0095 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1240+355C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762372 | ||||||
| chr2:185762469
|
T | C | 32 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(29): Show | 38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1240+452T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762469 | ||||||
| chr2:185762514
|
T | G | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1240+497T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762514 | ||||||
| chr2:185762597
|
T | G | 1 | a0038c0052t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1240+580T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762597 | ||||||
| chr2:185762643
|
A | G | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1241-540A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762643 | ||||||
| chr2:185762809
|
C | A | 93 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(90): Show | 109 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1241-374C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762809 | ||||||
| chr2:185762884
|
T | C | 10 | a0004c0004t0001g0005a0004c0004t0001g0068a0004c0004t0001g0069others(7): Show | 12 | HG00544.hp1 HG00558.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1241-299T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185762884 | ||||||
| chr2:185763163
|
G | A | 1 | a0013c0013t0002g0140 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1241-20G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 11/22 | chr2 | 185763163 | ||||||
| chr2:185763310
|
C | T | 1 | a0001c0001t0002g0158 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1347+21C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185763310 | ||||||
| chr2:185763476
|
G | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1347+187G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185763476 | ||||||
| chr2:185763745
|
G | A | 1 | a0003c0081t0001g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1347+456G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185763745 | ||||||
| chr2:185763778
|
G | T | 296 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(293): Show | 344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1347+489G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185763778 | ||||||
| chr2:185763974
|
T | C | 1 | a0005c0005t0001g0201 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1348-528T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185763974 | ||||||
| chr2:185764024
|
T | A | 3 | a0001c0051t0002g0104a0019c0024t0001g0236a0026c0029t0002g0170 | 3 | HG00597.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1348-478T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185764024 | ||||||
| chr2:185764090
|
TA | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1348-404delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr2 | 185764090 | |||||
| chr2:185764104
|
T | C | 3 | a0018c0021t0001g0023a0018c0021t0001g0197a0018c0021t0001g0198 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-398T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185764104 | ||||||
| chr2:185764112
|
A | T | 1 | a0002c0002t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1348-390A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185764112 | ||||||
| chr2:185764464
|
T | G | 101 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1348-38T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 12/22 | chr2 | 185764464 | ||||||
| chr2:185764595
|
T | A | 1 | a0013c0013t0002g0130 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1411+30T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764595 | ||||||
| chr2:185764604
|
C | A | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1411+39C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764604 | ||||||
| chr2:185764622
|
G | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+57G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764622 | ||||||
| chr2:185764655
|
T | C | 7 | a0019c0024t0001g0236a0019c0024t0001g0238a0019c0024t0001g0239others(4): Show | 7 | HG00544.hp2 HG00597.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411+90T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764655 | ||||||
| chr2:185764701
|
T | A | 4 | a0002c0018t0001g0027a0002c0018t0001g0241a0002c0018t0001g0242others(1): Show | 5 | NA18981.hp1 NA18984.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411+136T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764701 | ||||||
| chr2:185764822
|
A | G | 2 | a0003c0012t0003g0039a0003c0012t0003g0040 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1411+257A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764822 | ||||||
| chr2:185764846
|
A | G | 1 | a0002c0002t0001g0257 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1411+281A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764846 | ||||||
| chr2:185764948
|
C | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+383C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185764948 | ||||||
| chr2:185765074
|
G | A | 1 | a0003c0003t0001g0199 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1411+509G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765074 | ||||||
| chr2:185765130
|
C | T | 2 | a0008c0010t0002g0096a0008c0010t0002g0097 | 2 | HG00735.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.1411+565C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765130 | ||||||
| chr2:185765142
|
G | A | 4 | a0003c0012t0001g0192a0003c0012t0001g0193a0003c0012t0003g0039others(1): Show | 4 | HG02818.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+577G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765142 | ||||||
| chr2:185765195
|
A | T | 3 | a0001c0001t0002g0007a0001c0001t0002g0129a0040c0053t0002g0007 | 4 | HG02071.hp1 NA18967.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+630A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765195 | ||||||
| chr2:185765501
|
A | G | 1 | a0003c0003t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1411+936A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765501 | ||||||
| chr2:185765647
|
G | A | 10 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(7): Show | 11 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1411+1082G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765647 | ||||||
| chr2:185765660
|
G | A | 1 | a0004c0004t0001g0068 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1411+1095G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765660 | ||||||
| chr2:185765676
|
T | C | 34 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(31): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1411+1111T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765676 | ||||||
| chr2:185765711
|
T | C | 1 | a0037c0048t0001g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1411+1146T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765711 | ||||||
| chr2:185765734
|
C | A | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1411+1169C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765734 | ||||||
| chr2:185765741
|
G | A | 1 | a0006c0006t0002g0177 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1411+1176G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765741 | ||||||
| chr2:185765752
|
G | A | 99 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(96): Show | 114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1411+1187G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765752 | ||||||
| chr2:185765798
|
T | A | 3 | a0020c0020t0003g0013a0020c0020t0003g0062a0020c0020t0003g0063 | 4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+1233T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765798 | ||||||
| chr2:185765827
|
C | T | 3 | a0003c0003t0001g0308a0003c0003t0001g0309a0003c0003t0001g0310 | 3 | HG01123.hp1 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1411+1262C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765827 | ||||||
| chr2:185765928
|
T | C | 1 | a0045c0067t0001g0283 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1411+1363T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185765928 | ||||||
| chr2:185766391
|
T | C | 7 | a0003c0012t0001g0190a0003c0012t0001g0192a0003c0012t0001g0193others(4): Show | 7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411+1826T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766391 | ||||||
| chr2:185766399
|
A | G | 1 | a0012c0016t0001g0058 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1411+1834A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766399 | ||||||
| chr2:185766406
|
G | T | 133 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(130): Show | 154 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1411+1841G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766406 | ||||||
| chr2:185766436
|
A | T | 54 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(51): Show | 67 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1411+1871A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766436 | ||||||
| chr2:185766498
|
G | T | 3 | a0022c0025t0001g0022a0022c0025t0001g0188a0033c0035t0001g0042 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+1933G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766498 | ||||||
| chr2:185766503
|
T | C | 1 | a0004c0004t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1411+1938T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766503 | ||||||
| chr2:185766519
|
A | T | 1 | a0003c0003t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1411+1954A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766519 | ||||||
| chr2:185766587
|
T | G | 1 | a0003c0003t0001g0210 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1411+2022T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766587 | ||||||
| chr2:185766630
|
A | C | 34 | a0003c0066t0001g0288a0005c0005t0001g0011a0005c0005t0001g0032others(31): Show | 42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1411+2065A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766630 | ||||||
| chr2:185766700
|
A | G | 3 | a0010c0011t0002g0099a0010c0011t0002g0117a0010c0047t0002g0115 | 3 | HG02738.hp1 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1411+2135A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766700 | ||||||
| chr2:185766734
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1411+2169T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766734 | ||||||
| chr2:185766760
|
C | T | 146 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(143): Show | 172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1411+2195C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766760 | ||||||
| chr2:185766832
|
G | A | 1 | a0003c0076t0001g0265 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1411+2267G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766832 | ||||||
| chr2:185766834
|
C | T | 1 | a0062c0080t0003g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1411+2269C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766834 | ||||||
| chr2:185766851
|
A | G | 3 | a0003c0003t0001g0308a0003c0003t0001g0309a0003c0003t0001g0310 | 3 | HG01123.hp1 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1411+2286A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766851 | ||||||
| chr2:185766862
|
C | T | 164 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(161): Show | 191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1411+2297C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766862 | ||||||
| chr2:185766864
|
C | T | 1 | a0062c0080t0003g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1411+2299C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766864 | ||||||
| chr2:185766881
|
T | C | 1 | a0062c0080t0003g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1411+2316T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185766881 | ||||||
| chr2:185767044
|
C | G | 1 | a0025c0030t0002g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1411+2479C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767044 | ||||||
| chr2:185767062
|
G | A | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1411+2497G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767062 | ||||||
| chr2:185767099
|
A | G | 3 | a0003c0012t0001g0190a0003c0012t0001g0195a0003c0075t0001g0189 | 3 | HG02970.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1411+2534A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767099 | ||||||
| chr2:185767110
|
T | C | 3 | a0022c0025t0001g0022a0022c0025t0001g0188a0033c0035t0001g0042 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+2545T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767110 | ||||||
| chr2:185767130
|
G | A | 5 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1411+2565G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767130 | ||||||
| chr2:185767198
|
C | T | 4 | a0018c0021t0001g0023a0018c0021t0001g0197a0018c0021t0001g0198others(1): Show | 6 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411+2633C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767198 | ||||||
| chr2:185767201
|
G | C | 3 | a0020c0020t0003g0013a0020c0020t0003g0062a0020c0020t0003g0063 | 4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+2636G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767201 | ||||||
| chr2:185767218
|
A | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+2653A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767218 | ||||||
| chr2:185767331
|
T | A | 3 | a0020c0020t0003g0013a0020c0020t0003g0062a0020c0020t0003g0063 | 4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+2766T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767331 | ||||||
| chr2:185767369
|
A | C | 1 | a0003c0012t0001g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1411+2804A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767369 | ||||||
| chr2:185767430
|
C | T | 9 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(6): Show | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1411+2865C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767430 | ||||||
| chr2:185767513
|
T | C | 3 | a0003c0012t0001g0190a0003c0012t0001g0195a0003c0075t0001g0189 | 3 | HG02970.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1411+2948T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767513 | ||||||
| chr2:185767528
|
T | A | 19 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0269others(16): Show | 21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1411+2963T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767528 | ||||||
| chr2:185767540
|
T | C | 1 | a0003c0003t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1411+2975T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767540 | ||||||
| chr2:185767647
|
T | A | 2 | a0001c0001t0002g0119a0032c0045t0002g0120 | 2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1411+3082T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767647 | ||||||
| chr2:185767793
|
T | G | 1 | a0004c0004t0001g0081 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1411+3228T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767793 | ||||||
| chr2:185767914
|
G | A | 1 | a0005c0005t0001g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1411+3349G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185767914 | ||||||
| chr2:185768121
|
T | A | 1 | a0051c0064t0001g0243 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1411+3556T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768121 | ||||||
| chr2:185768349
|
A | G | 2 | a0001c0043t0002g0127a0008c0010t0002g0128 | 2 | NA18959.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1411+3784A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768349 | ||||||
| chr2:185768528
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+3963A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768528 | ||||||
| chr2:185768665
|
C | T | 1 | a0009c0009t0001g0298 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1411+4100C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768665 | ||||||
| chr2:185768798
|
A | G | 162 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(159): Show | 189 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1411+4233A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768798 | ||||||
| chr2:185768892
|
T | C | 1 | a0003c0012t0001g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1411+4327T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768892 | ||||||
| chr2:185768941
|
T | C | 27 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(24): Show | 31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1411+4376T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768941 | ||||||
| chr2:185768990
|
T | C | 197 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(194): Show | 230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1411+4425T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185768990 | ||||||
| chr2:185769102
|
C | T | 4 | a0001c0001t0002g0157a0018c0021t0001g0023a0018c0021t0001g0197others(1): Show | 5 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1411+4537C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185769102 | ||||||
| chr2:185769292
|
C | T | 1 | a0020c0020t0003g0063 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1411+4727C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185769292 | ||||||
| chr2:185769824
|
G | A | 1 | a0004c0004t0001g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1411+5259G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185769824 | ||||||
| chr2:185769844
|
T | G | 1 | a0001c0001t0002g0141 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1411+5279T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185769844 | ||||||
| chr2:185769970
|
T | G | 1 | a0001c0001t0002g0135 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1411+5405T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185769970 | ||||||
| chr2:185770122
|
G | C | 101 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1411+5557G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770122 | ||||||
| chr2:185770122
|
G | T | 1 | a0046c0071t0001g0221 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1411+5557G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770122 | ||||||
| chr2:185770126
|
G | A | 1 | a0046c0071t0001g0221 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1411+5561G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770126 | ||||||
| chr2:185770200
|
A | G | 19 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0269others(16): Show | 21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1411+5635A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770200 | ||||||
| chr2:185770241
|
G | C | 1 | a0003c0003t0001g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1411+5676G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770241 | ||||||
| chr2:185770360
|
T | C | 1 | a0003c0003t0001g0308 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1411+5795T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770360 | ||||||
| chr2:185770388
|
G | A | 1 | a0033c0035t0001g0042 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1411+5823G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770388 | ||||||
| chr2:185770821
|
T | C | 1 | a0016c0022t0002g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1411+6256T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185770821 | ||||||
| chr2:185771002
|
C | T | 9 | a0006c0006t0001g0031a0006c0006t0001g0273a0006c0006t0001g0274others(6): Show | 10 | HG01099.hp1 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1411+6437C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771002 | ||||||
| chr2:185771033
|
C | G | 1 | a0005c0005t0001g0297 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1411+6468C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771033 | ||||||
| chr2:185771142
|
T | A | 1 | a0003c0075t0001g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1411+6577T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771142 | ||||||
| chr2:185771184
|
G | A | 7 | a0003c0012t0001g0190a0003c0012t0001g0192a0003c0012t0001g0193others(4): Show | 7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411+6619G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771184 | ||||||
| chr2:185771324
|
G | A | 7 | a0003c0012t0001g0190a0003c0012t0001g0192a0003c0012t0001g0193others(4): Show | 7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411+6759G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771324 | ||||||
| chr2:185771350
|
G | T | 34 | a0003c0066t0001g0288a0005c0005t0001g0011a0005c0005t0001g0032others(31): Show | 42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1411+6785G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771350 | ||||||
| chr2:185771356
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+6791A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771356 | ||||||
| chr2:185771606
|
A | G | 1 | a0016c0022t0002g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1411+7041A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771606 | ||||||
| chr2:185771607
|
A | G | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1411+7042A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771607 | ||||||
| chr2:185771615
|
C | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+7050C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185771615 | ||||||
| chr2:185772124
|
C | T | 4 | a0020c0020t0003g0013a0020c0020t0003g0062a0020c0020t0003g0063others(1): Show | 5 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411+7559C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772124 | ||||||
| chr2:185772145
|
T | A | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1411+7580T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772145 | ||||||
| chr2:185772431
|
G | A | 2 | a0003c0003t0001g0014a0047c0074t0001g0212 | 3 | HG01081.hp2 HG02300.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1411+7866G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772431 | ||||||
| chr2:185772568
|
A | G | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1411+8003A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772568 | ||||||
| chr2:185772584
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1411+8019C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772584 | ||||||
| chr2:185772589
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+8024C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772589 | ||||||
| chr2:185772757
|
T | C | 102 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(99): Show | 117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1411+8192T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772757 | ||||||
| chr2:185772759
|
A | G | 102 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(99): Show | 117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1411+8194A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772759 | ||||||
| chr2:185772775
|
G | A | 3 | a0022c0025t0001g0022a0022c0025t0001g0188a0033c0035t0001g0042 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+8210G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772775 | ||||||
| chr2:185772788
|
T | A | 1 | a0037c0048t0001g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1411+8223T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772788 | ||||||
| chr2:185772804
|
T | TCCTCC | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1411+8250_1411+825 others(9): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185772804 | |||||
| chr2:185772843
|
C | T | 1 | a0002c0002t0001g0256 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1411+8278C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772843 | ||||||
| chr2:185772983
|
C | T | 3 | a0020c0020t0003g0013a0020c0020t0003g0062a0020c0020t0003g0063 | 4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+8418C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185772983 | ||||||
| chr2:185773106
|
T | C | 1 | a0002c0002t0001g0036 | 2 | HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1411+8541T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773106 | ||||||
| chr2:185773153
|
C | T | 2 | a0025c0030t0002g0116a0025c0030t0002g0183 | 2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1411+8588C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773153 | ||||||
| chr2:185773207
|
G | A | 1 | a0027c0033t0001g0311 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1411+8642G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773207 | ||||||
| chr2:185773283
|
T | C | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1411+8718T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773283 | ||||||
| chr2:185773324
|
A | G | 2 | a0003c0072t0001g0184a0048c0073t0001g0275 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1411+8759A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773324 | ||||||
| chr2:185773327
|
C | G | 1 | a0003c0003t0001g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1411+8762C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773327 | ||||||
| chr2:185773333
|
T | C | 2 | a0003c0072t0001g0184a0048c0073t0001g0275 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1411+8768T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773333 | ||||||
| chr2:185773712
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-8993C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773712 | ||||||
| chr2:185773747
|
T | C | 2 | a0022c0025t0001g0022a0022c0025t0001g0188 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1412-8958T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773747 | ||||||
| chr2:185773835
|
G | A | 9 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(6): Show | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412-8870G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773835 | ||||||
| chr2:185773939
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-8766A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185773939 | ||||||
| chr2:185774434
|
C | T | 7 | a0003c0012t0001g0190a0003c0012t0001g0192a0003c0012t0001g0193others(4): Show | 7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412-8271C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774434 | ||||||
| chr2:185774503
|
C | CTAAT | 102 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(99): Show | 117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1412-8200_1412-819 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185774503 | |||||
| chr2:185774512
|
T | C | 102 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(99): Show | 117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1412-8193T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774512 | ||||||
| chr2:185774581
|
ATT | A | 160 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(157): Show | 186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1412-8113_1412-811 others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185774581 | |||||
| chr2:185774648
|
G | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-8057G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774648 | ||||||
| chr2:185774690
|
C | A | 1 | a0003c0003t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1412-8015C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774690 | ||||||
| chr2:185774730
|
C | G | 2 | a0005c0005t0001g0201a0005c0005t0001g0296 | 2 | HG02015.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1412-7975C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774730 | ||||||
| chr2:185774768
|
T | C | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | NA18961.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1412-7937T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774768 | ||||||
| chr2:185774822
|
A | T | 3 | a0004c0004t0002g0019a0004c0004t0002g0173a0004c0004t0002g0174 | 4 | NA18953.hp2 NA18967.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-7883A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774822 | ||||||
| chr2:185774828
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-7877A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774828 | ||||||
| chr2:185774847
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-7858C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774847 | ||||||
| chr2:185774872
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-7833A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774872 | ||||||
| chr2:185774879
|
A | G | 32 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(29): Show | 38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1412-7826A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774879 | ||||||
| chr2:185774916
|
A | C | 102 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(99): Show | 117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1412-7789A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774916 | ||||||
| chr2:185774955
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-7750T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185774955 | ||||||
| chr2:185775008
|
T | A | 1 | a0016c0022t0002g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1412-7697T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775008 | ||||||
| chr2:185775026
|
A | G | 32 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(29): Show | 38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1412-7679A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775026 | ||||||
| chr2:185775031
|
G | A | 1 | a0002c0002t0001g0257 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1412-7674G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775031 | ||||||
| chr2:185775040
|
A | C | 102 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(99): Show | 117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1412-7665A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775040 | ||||||
| chr2:185775080
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-7625C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775080 | ||||||
| chr2:185775210
|
C | T | 2 | a0001c0001t0002g0155a0060c0079t0001g0191 | 2 | HG02300.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1412-7495C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775210 | ||||||
| chr2:185775211
|
G | A | 7 | a0003c0012t0001g0190a0003c0012t0001g0192a0003c0012t0001g0193others(4): Show | 7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412-7494G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775211 | ||||||
| chr2:185775232
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1412-7473C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775232 | ||||||
| chr2:185775327
|
T | G | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1412-7378T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775327 | ||||||
| chr2:185775503
|
G | A | 162 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(159): Show | 189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1412-7202G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775503 | ||||||
| chr2:185775548
|
A | G | 1 | a0003c0012t0001g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1412-7157A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775548 | ||||||
| chr2:185775647
|
G | C | 3 | a0001c0001t0002g0135a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | NA19082.hp2 NA19085.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1412-7058G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775647 | ||||||
| chr2:185775656
|
TTTTG | T | 3 | a0020c0020t0003g0013a0020c0020t0003g0062a0020c0020t0003g0063 | 4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-7037_1412-703 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185775656 | |||||
| chr2:185775682
|
T | G | 1 | a0038c0052t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1412-7023T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775682 | ||||||
| chr2:185775813
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-6892A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775813 | ||||||
| chr2:185775873
|
A | C | 2 | a0001c0001t0002g0118a0001c0001t0002g0126 | 2 | HG00423.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1412-6832A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775873 | ||||||
| chr2:185775883
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-6822T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775883 | ||||||
| chr2:185775943
|
G | A | 1 | a0044c0068t0001g0285 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1412-6762G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775943 | ||||||
| chr2:185775984
|
A | G | 3 | a0018c0021t0001g0023a0018c0021t0001g0197a0018c0021t0001g0198 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-6721A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185775984 | ||||||
| chr2:185776008
|
G | A | 2 | a0001c0001t0002g0142a0001c0001t0002g0156 | 2 | NA18945.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1412-6697G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776008 | ||||||
| chr2:185776024
|
C | T | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1412-6681C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776024 | ||||||
| chr2:185776041
|
G | A | 1 | a0057c0055t0001g0280 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1412-6664G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776041 | ||||||
| chr2:185776050
|
G | A | 19 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0269others(16): Show | 21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1412-6655G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776050 | ||||||
| chr2:185776109
|
A | G | 1 | a0005c0005t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1412-6596A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776109 | ||||||
| chr2:185776203
|
A | G | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1412-6502A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776203 | ||||||
| chr2:185776212
|
G | T | 1 | a0038c0052t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1412-6493G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776212 | ||||||
| chr2:185776269
|
C | G | 1 | a0005c0005t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1412-6436C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776269 | ||||||
| chr2:185776298
|
AAATTAT | A | 3 | a0003c0012t0001g0190a0003c0012t0001g0195a0003c0075t0001g0189 | 3 | HG02970.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1412-6403_1412-639 others(10): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185776298 | |||||
| chr2:185776309
|
A | T | 19 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0269others(16): Show | 21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1412-6396A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776309 | ||||||
| chr2:185776401
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-6304C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776401 | ||||||
| chr2:185776449
|
C | T | 1 | a0005c0005t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1412-6256C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776449 | ||||||
| chr2:185776467
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-6238C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776467 | ||||||
| chr2:185776485
|
A | T | 25 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(22): Show | 29 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1412-6220A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776485 | ||||||
| chr2:185776542
|
A | G | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1412-6163A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776542 | ||||||
| chr2:185776694
|
A | G | 1 | a0001c0001t0002g0163 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1412-6011A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776694 | ||||||
| chr2:185776746
|
T | C | 7 | a0003c0012t0001g0190a0003c0012t0001g0192a0003c0012t0001g0193others(4): Show | 7 | HG02818.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412-5959T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776746 | ||||||
| chr2:185776801
|
C | T | 1 | a0002c0002t0001g0257 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1412-5904C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776801 | ||||||
| chr2:185776805
|
G | C | 2 | a0007c0007t0001g0045a0007c0007t0001g0046 | 2 | HG00423.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1412-5900G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185776805 | ||||||
| chr2:185777009
|
C | G | 1 | a0003c0003t0001g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1412-5696C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777009 | ||||||
| chr2:185777393
|
G | GT | 11 | a0003c0012t0001g0192a0003c0012t0001g0193a0003c0012t0003g0040others(8): Show | 11 | HG00544.hp1 HG01261.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-5294dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185777393 | |||||
| chr2:185777393
|
GT | G | 143 | a0001c0001t0002g0018a0001c0001t0002g0129a0001c0001t0002g0134others(140): Show | 168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1412-5294delT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185777393 | |||||
| chr2:185777393
|
GTT | G | 79 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0016others(76): Show | 87 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1412-5295_1412-529 others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185777393 | |||||
| chr2:185777393
|
GTTT | G | 22 | a0001c0001t0002g0003a0001c0001t0002g0089a0001c0001t0002g0108others(19): Show | 30 | HG00323.hp1 HG01255.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1412-5296_1412-529 others(7): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185777393 | |||||
| chr2:185777420
|
C | A | 2 | a0003c0012t0001g0190a0003c0075t0001g0189 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1412-5285C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777420 | ||||||
| chr2:185777439
|
G | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-5266G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777439 | ||||||
| chr2:185777625
|
T | G | 2 | a0001c0001t0002g0123a0001c0001t0002g0143 | 2 | NA18941.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1412-5080T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777625 | ||||||
| chr2:185777637
|
A | G | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1412-5068A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777637 | ||||||
| chr2:185777711
|
C | T | 1 | a0003c0003t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1412-4994C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777711 | ||||||
| chr2:185777826
|
T | C | 3 | a0022c0025t0001g0022a0022c0025t0001g0188a0033c0035t0001g0042 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-4879T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777826 | ||||||
| chr2:185777837
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-4868A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777837 | ||||||
| chr2:185777848
|
C | A | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1412-4857C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777848 | ||||||
| chr2:185777862
|
C | A | 1 | a0002c0002t0001g0244 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1412-4843C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185777862 | ||||||
| chr2:185778089
|
G | T | 195 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(192): Show | 228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1412-4616G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185778089 | ||||||
| chr2:185778546
|
T | G | 1 | a0005c0005t0001g0032 | 2 | HG01175.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1412-4159T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185778546 | ||||||
| chr2:185778912
|
G | C | 34 | a0003c0066t0001g0288a0005c0005t0001g0011a0005c0005t0001g0032others(31): Show | 42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1412-3793G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185778912 | ||||||
| chr2:185778950
|
A | G | 1 | a0001c0008t0002g0146 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1412-3755A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185778950 | ||||||
| chr2:185779061
|
T | C | 1 | a0001c0001t0002g0089 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1412-3644T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779061 | ||||||
| chr2:185779075
|
G | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-3630G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779075 | ||||||
| chr2:185779077
|
T | G | 1 | a0003c0012t0001g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1412-3628T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779077 | ||||||
| chr2:185779300
|
G | GT | 159 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(156): Show | 186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1412-3395dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185779300 | |||||
| chr2:185779541
|
T | C | 110 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(107): Show | 126 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1412-3164T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779541 | ||||||
| chr2:185779549
|
T | C | 112 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(109): Show | 130 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1412-3156T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779549 | ||||||
| chr2:185779666
|
G | T | 32 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(29): Show | 38 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1412-3039G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779666 | ||||||
| chr2:185779668
|
TTTC | T | 3 | a0010c0011t0002g0099a0010c0011t0002g0117a0010c0047t0002g0115 | 3 | HG02738.hp1 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1412-3034_1412-303 others(7): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185779668 | |||||
| chr2:185779677
|
ATT | A | 3 | a0016c0022t0002g0180a0016c0022t0002g0182a0016c0038t0002g0181 | 3 | HG02630.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1412-3027_1412-302 others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779677 | ||||||
| chr2:185779824
|
C | T | 1 | a0002c0002t0001g0256 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1412-2881C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185779824 | ||||||
| chr2:185780039
|
C | T | 1 | a0005c0005t0001g0307 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1412-2666C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780039 | ||||||
| chr2:185780072
|
C | CA | 16 | a0002c0002t0001g0006a0002c0002t0001g0026a0002c0002t0001g0084others(13): Show | 18 | HG01192.hp1 HG01361.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1412-2619dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185780072 | |||||
| chr2:185780072
|
C | CAA | 7 | a0010c0011t0002g0099a0010c0011t0002g0105a0010c0011t0002g0106others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412-2620_1412-261 others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185780072 | |||||
| chr2:185780082
|
A | T | 2 | a0001c0001t0002g0145a0001c0001t0002g0158 | 2 | NA18966.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1412-2623A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780082 | ||||||
| chr2:185780164
|
C | T | 1 | a0006c0006t0001g0274 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1412-2541C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780164 | ||||||
| chr2:185780253
|
A | T | 1 | a0054c0058t0001g0261 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1412-2452A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780253 | ||||||
| chr2:185780256
|
T | C | 6 | a0003c0003t0001g0213a0003c0003t0001g0214a0003c0003t0001g0215others(3): Show | 6 | HG02135.hp2 NA18747.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412-2449T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780256 | ||||||
| chr2:185780407
|
T | C | 2 | a0005c0005t0001g0286a0005c0005t0001g0300 | 2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1412-2298T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780407 | ||||||
| chr2:185780567
|
C | CT | 27 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(24): Show | 31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1412-2136dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185780567 | |||||
| chr2:185780570
|
C | T | 27 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(24): Show | 31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1412-2135C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780570 | ||||||
| chr2:185780574
|
A | T | 27 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(24): Show | 31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1412-2131A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780574 | ||||||
| chr2:185780723
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-1982A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185780723 | ||||||
| chr2:185780987
|
T | TATC | 4 | a0005c0005t0001g0303a0005c0005t0001g0305a0023c0028t0001g0034others(1): Show | 5 | HG01261.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412-1717_1412-171 others(7): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185780987 | |||||
| chr2:185781044
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-1661T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781044 | ||||||
| chr2:185781058
|
G | T | 25 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(22): Show | 29 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1412-1647G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781058 | ||||||
| chr2:185781059
|
A | AT | 150 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(147): Show | 176 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1412-1633dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185781059 | |||||
| chr2:185781126
|
GACTT | G | 195 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(192): Show | 228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1412-1572_1412-156 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185781126 | |||||
| chr2:185781434
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-1271T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781434 | ||||||
| chr2:185781441
|
G | A | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1412-1264G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781441 | ||||||
| chr2:185781443
|
G | T | 2 | a0002c0002t0001g0252a0002c0002t0001g0253 | 2 | NA19054.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1412-1262G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781443 | ||||||
| chr2:185781465
|
C | T | 195 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(192): Show | 228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1412-1240C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781465 | ||||||
| chr2:185781527
|
G | A | 1 | a0004c0004t0002g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1412-1178G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781527 | ||||||
| chr2:185781843
|
C | CT | 159 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(156): Show | 185 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1412-850dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185781843 | |||||
| chr2:185781900
|
C | T | 1 | a0001c0001t0002g0124 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1412-805C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781900 | ||||||
| chr2:185781912
|
A | G | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1412-793A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781912 | ||||||
| chr2:185781959
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-746T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781959 | ||||||
| chr2:185781963
|
C | G | 8 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(5): Show | 9 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-742C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185781963 | ||||||
| chr2:185782004
|
C | A | 1 | a0004c0004t0001g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1412-701C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185782004 | ||||||
| chr2:185782076
|
T | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1412-629T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185782076 | ||||||
| chr2:185782202
|
A | G | 9 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(6): Show | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412-503A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185782202 | ||||||
| chr2:185782218
|
A | T | 2 | a0005c0005t0001g0033a0005c0005t0001g0295 | 3 | HG03688.hp1 HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1412-487A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185782218 | ||||||
| chr2:185782294
|
TTCAGGTA | T | 153 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(150): Show | 179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1412-410_1412-404d others(9): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185782294 | ||||||
| chr2:185782431
|
C | T | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1412-274C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | chr2 | 185782431 | ||||||
| chr2:185782543
|
T | TA | 34 | a0003c0066t0001g0288a0005c0005t0001g0011a0005c0005t0001g0032others(31): Show | 42 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1412-161dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 185782543 | |||||
| chr2:185782845
|
G | A | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1469+83G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185782845 | ||||||
| chr2:185782941
|
T | C | 2 | a0001c0001t0002g0123a0001c0001t0002g0143 | 2 | NA18941.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1469+179T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185782941 | ||||||
| chr2:185783174
|
C | A | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1469+412C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185783174 | ||||||
| chr2:185783742
|
G | C | 5 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469+980G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185783742 | ||||||
| chr2:185783913
|
A | G | 1 | a0004c0004t0001g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1469+1151A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185783913 | ||||||
| chr2:185783942
|
C | G | 3 | a0020c0020t0003g0013a0020c0020t0003g0062a0020c0020t0003g0063 | 4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469+1180C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185783942 | ||||||
| chr2:185784069
|
T | C | 1 | a0050c0065t0001g0287 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1469+1307T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185784069 | ||||||
| chr2:185784125
|
T | A | 1 | a0013c0013t0002g0147 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1469+1363T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185784125 | ||||||
| chr2:185784168
|
T | C | 1 | a0013c0013t0002g0147 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1469+1406T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185784168 | ||||||
| chr2:185784191
|
G | C | 1 | a0013c0013t0002g0147 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1469+1429G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185784191 | ||||||
| chr2:185784247
|
G | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1469+1485G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185784247 | ||||||
| chr2:185784606
|
A | C | 1 | a0003c0003t0001g0308 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1470-1646A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185784606 | ||||||
| chr2:185785210
|
T | C | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1470-1042T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185785210 | ||||||
| chr2:185785261
|
T | G | 1 | a0006c0069t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1470-991T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185785261 | ||||||
| chr2:185785569
|
A | ATATT | 103 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(100): Show | 118 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1470-677_1470-674d others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr2 | 185785569 | |||||
| chr2:185785653
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1470-599C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185785653 | ||||||
| chr2:185785685
|
T | C | 162 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(159): Show | 189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1470-567T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185785685 | ||||||
| chr2:185785736
|
C | CTT | 3 | a0022c0025t0001g0022a0022c0025t0001g0188a0033c0035t0001g0042 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1470-515_1470-514d others(4): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr2 | 185785736 | |||||
| chr2:185785938
|
T | C | 1 | a0062c0080t0003g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1470-314T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185785938 | ||||||
| chr2:185786171
|
T | A | 3 | a0018c0021t0001g0023a0018c0021t0001g0197a0018c0021t0001g0198 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1470-81T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 14/22 | chr2 | 185786171 | ||||||
| chr2:185786425
|
C | T | 3 | a0022c0025t0001g0022a0022c0025t0001g0188a0033c0035t0001g0042 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506+137C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786425 | ||||||
| chr2:185786510
|
C | T | 54 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(51): Show | 67 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1506+222C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786510 | ||||||
| chr2:185786543
|
A | G | 9 | a0016c0022t0002g0178a0016c0022t0002g0179a0016c0022t0002g0180others(6): Show | 10 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1506+255A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786543 | ||||||
| chr2:185786654
|
G | A | 102 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(99): Show | 117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1506+366G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786654 | ||||||
| chr2:185786660
|
T | C | 25 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(22): Show | 29 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1506+372T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786660 | ||||||
| chr2:185786784
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1506+496C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786784 | ||||||
| chr2:185786834
|
C | T | 1 | a0006c0006t0001g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1506+546C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786834 | ||||||
| chr2:185786891
|
T | C | 1 | a0019c0024t0001g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1506+603T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786891 | ||||||
| chr2:185786915
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1506+627C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786915 | ||||||
| chr2:185786926
|
A | C | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1506+638A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786926 | ||||||
| chr2:185786937
|
A | G | 1 | a0003c0003t0001g0014 | 2 | HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1506+649A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786937 | ||||||
| chr2:185786958
|
T | A | 4 | a0003c0012t0001g0192a0003c0012t0001g0193a0003c0012t0003g0039others(1): Show | 4 | HG02818.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506+670T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786958 | ||||||
| chr2:185786982
|
C | T | 4 | a0003c0012t0001g0192a0003c0012t0001g0193a0003c0012t0003g0039others(1): Show | 4 | HG02818.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506+694C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185786982 | ||||||
| chr2:185787032
|
G | A | 146 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(143): Show | 172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1506+744G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787032 | ||||||
| chr2:185787173
|
G | C | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1506+885G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787173 | ||||||
| chr2:185787183
|
T | A | 2 | a0002c0002t0001g0245a0002c0002t0001g0246 | 2 | HG00639.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1506+895T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787183 | ||||||
| chr2:185787199
|
A | G | 1 | a0006c0069t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1506+911A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787199 | ||||||
| chr2:185787232
|
T | TAAG | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1506+946_1506+948d others(5): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr2 | 185787232 | |||||
| chr2:185787242
|
A | G | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1506+954A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787242 | ||||||
| chr2:185787644
|
G | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1507-999G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787644 | ||||||
| chr2:185787849
|
C | T | 19 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0269others(16): Show | 21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1507-794C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787849 | ||||||
| chr2:185787884
|
T | G | 2 | a0007c0007t0001g0045a0007c0007t0001g0046 | 2 | HG00423.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1507-759T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787884 | ||||||
| chr2:185787982
|
T | C | 1 | a0003c0003t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1507-661T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185787982 | ||||||
| chr2:185788089
|
A | G | 3 | a0001c0001t0002g0133a0001c0001t0002g0155a0001c0001t0002g0159 | 3 | HG01496.hp2 HG02300.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1507-554A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788089 | ||||||
| chr2:185788091
|
A | G | 10 | a0004c0004t0001g0005a0004c0004t0001g0068a0004c0004t0001g0069others(7): Show | 12 | HG00544.hp1 HG00558.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1507-552A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788091 | ||||||
| chr2:185788119
|
G | T | 1 | a0002c0002t0001g0251 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1507-524G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788119 | ||||||
| chr2:185788164
|
C | G | 1 | a0002c0002t0001g0026 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1507-479C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788164 | ||||||
| chr2:185788220
|
A | C | 1 | a0002c0057t0001g0250 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1507-423A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788220 | ||||||
| chr2:185788300
|
T | C | 1 | a0001c0001t0002g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1507-343T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788300 | ||||||
| chr2:185788631
|
C | T | 4 | a0019c0024t0001g0238a0024c0034t0001g0037a0024c0034t0001g0237others(1): Show | 4 | HG00544.hp2 NA18959.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1507-12C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 15/22 | chr2 | 185788631 | ||||||
| chr2:185797735
|
C | A | 1 | a0001c0001t0002g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.10390+209C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185797735 | ||||||
| chr2:185797759
|
G | T | 1 | a0003c0003t0001g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.10390+233G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185797759 | ||||||
| chr2:185797917
|
C | G | 1 | a0002c0002t0001g0233 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.10390+391C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185797917 | ||||||
| chr2:185798039
|
A | G | 3 | a0022c0025t0001g0022a0022c0025t0001g0188a0033c0035t0001g0042 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.10390+513A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798039 | ||||||
| chr2:185798049
|
G | A | 1 | a0005c0005t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.10390+523G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798049 | ||||||
| chr2:185798068
|
T | C | 1 | a0012c0016t0001g0056 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.10390+542T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798068 | ||||||
| chr2:185798109
|
G | C | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.10390+583G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798109 | ||||||
| chr2:185798216
|
C | G | 1 | a0005c0005t0001g0296 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.10390+690C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798216 | ||||||
| chr2:185798228
|
C | A | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.10390+702C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798228 | ||||||
| chr2:185798271
|
A | C | 100 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.10390+745A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798271 | ||||||
| chr2:185798406
|
CAT | C | 3 | a0006c0006t0001g0277a0006c0006t0001g0278a0006c0006t0001g0279 | 3 | HG02280.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10390+881_10390+88 others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798406 | ||||||
| chr2:185798428
|
C | T | 1 | a0003c0003t0001g0215 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.10390+902C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798428 | ||||||
| chr2:185798670
|
G | A | 34 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(31): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.10391-1027G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798670 | ||||||
| chr2:185798810
|
T | A | 3 | a0022c0025t0001g0022a0022c0025t0001g0188a0033c0035t0001g0042 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.10391-887T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798810 | ||||||
| chr2:185798813
|
A | G | 4 | a0006c0006t0001g0030a0006c0006t0001g0268a0006c0006t0001g0270others(1): Show | 5 | HG02055.hp2 HG02723.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.10391-884A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185798813 | ||||||
| chr2:185799052
|
C | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.10391-645C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185799052 | ||||||
| chr2:185799563
|
C | A | 14 | a0006c0006t0001g0030a0006c0006t0001g0031a0006c0006t0001g0268others(11): Show | 16 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.10391-134C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 16/22 | chr2 | 185799563 | ||||||
| chr2:185809178
|
A | T | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.19827+45A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185809178 | ||||||
| chr2:185809492
|
C | T | 34 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(31): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.19827+359C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185809492 | ||||||
| chr2:185809500
|
A | G | 1 | a0008c0010t0002g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19827+367A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185809500 | ||||||
| chr2:185809696
|
A | G | 1 | a0011c0017t0001g0055 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.19827+563A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185809696 | ||||||
| chr2:185809705
|
G | T | 1 | a0001c0001t0002g0132 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.19827+572G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185809705 | ||||||
| chr2:185809759
|
A | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.19827+626A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185809759 | ||||||
| chr2:185810002
|
C | A | 1 | a0003c0012t0001g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.19827+869C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810002 | ||||||
| chr2:185810018
|
G | A | 4 | a0003c0003t0001g0216a0003c0003t0001g0223a0003c0003t0001g0226others(1): Show | 4 | HG02132.hp1 NA18612.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.19827+885G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810018 | ||||||
| chr2:185810244
|
A | G | 34 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(31): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.19827+1111A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810244 | ||||||
| chr2:185810469
|
G | T | 1 | a0002c0002t0001g0262 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.19827+1336G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810469 | ||||||
| chr2:185810506
|
A | C | 1 | a0003c0003t0001g0223 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.19827+1373A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810506 | ||||||
| chr2:185810537
|
CT | C | 123 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(120): Show | 144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.19827+1430delT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185810537 | |||||
| chr2:185810537
|
CTT | C | 9 | a0001c0001t0002g0148a0004c0004t0001g0073a0004c0004t0001g0074others(6): Show | 10 | HG01168.hp1 HG01169.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.19827+1429_19827+1 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185810537 | |||||
| chr2:185810537
|
CTTTTTTT | C | 5 | a0002c0002t0001g0026a0002c0062t0001g0231a0006c0006t0001g0277others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.19827+1424_19827+1 others(13): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185810537 | |||||
| chr2:185810537
|
CTTTTTTT others(1): Show |
C | 136 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(133): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.19827+1423_19827+1 others(14): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185810537 | |||||
| chr2:185810537
|
CTTTTTTT others(3): Show |
C | 1 | a0011c0017t0001g0047 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.19827+1421_19827+1 others(16): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185810537 | |||||
| chr2:185810563
|
T | A | 1 | a0003c0003t0001g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.19827+1430T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810563 | ||||||
| chr2:185810578
|
C | T | 101 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.19827+1445C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810578 | ||||||
| chr2:185810594
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.19827+1461C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810594 | ||||||
| chr2:185810623
|
A | G | 1 | a0004c0004t0001g0070 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.19827+1490A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810623 | ||||||
| chr2:185810723
|
C | CCT | 34 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(31): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.19827+1593_19827+1 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185810723 | |||||
| chr2:185810774
|
T | C | 1 | a0010c0047t0002g0115 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.19827+1641T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810774 | ||||||
| chr2:185810847
|
T | G | 1 | a0005c0005t0001g0304 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.19827+1714T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185810847 | ||||||
| chr2:185811100
|
TATTCTCA others(5): Show |
T | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19827+1969_19827+1 others(18): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185811100 | |||||
| chr2:185811144
|
T | G | 1 | a0002c0002t0001g0244 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.19827+2011T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811144 | ||||||
| chr2:185811175
|
T | C | 2 | a0014c0014t0002g0101a0014c0014t0002g0102 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.19827+2042T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811175 | ||||||
| chr2:185811351
|
C | T | 6 | a0009c0009t0001g0012a0009c0009t0001g0293a0009c0009t0001g0294others(3): Show | 8 | HG01167.hp2 HG01169.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.19828-2194C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811351 | ||||||
| chr2:185811468
|
C | CA | 16 | a0001c0001t0002g0018a0001c0001t0002g0155a0002c0002t0001g0245others(13): Show | 17 | HG00741.hp2 HG01081.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.19828-2060dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185811468 | |||||
| chr2:185811496
|
C | T | 1 | a0009c0009t0001g0298 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.19828-2049C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811496 | ||||||
| chr2:185811519
|
GTTGT | G | 4 | a0002c0002t0001g0028a0002c0002t0001g0251a0002c0002t0001g0259others(1): Show | 6 | NA18951.hp1 NA18961.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.19828-2003_19828-2 others(10): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185811519 | |||||
| chr2:185811523
|
T | G | 1 | a0003c0003t0001g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.19828-2022T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811523 | ||||||
| chr2:185811611
|
G | A | 1 | a0009c0009t0001g0293 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.19828-1934G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811611 | ||||||
| chr2:185811679
|
C | T | 13 | a0006c0006t0001g0030a0006c0006t0001g0031a0006c0006t0001g0268others(10): Show | 15 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.19828-1866C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811679 | ||||||
| chr2:185811990
|
G | A | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.19828-1555G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811990 | ||||||
| chr2:185811995
|
A | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.19828-1550A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185811995 | ||||||
| chr2:185812010
|
G | A | 1 | a0009c0009t0001g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.19828-1535G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812010 | ||||||
| chr2:185812054
|
T | C | 1 | a0001c0001t0002g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.19828-1491T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812054 | ||||||
| chr2:185812118
|
C | T | 5 | a0005c0005t0001g0035a0005c0005t0001g0290a0005c0005t0001g0291others(2): Show | 6 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.19828-1427C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812118 | ||||||
| chr2:185812286
|
C | T | 1 | a0002c0002t0001g0263 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.19828-1259C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812286 | ||||||
| chr2:185812297
|
A | T | 1 | a0008c0010t0002g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19828-1248A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812297 | ||||||
| chr2:185812339
|
G | A | 2 | a0002c0002t0001g0245a0002c0002t0001g0246 | 2 | HG00639.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.19828-1206G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812339 | ||||||
| chr2:185812386
|
C | T | 4 | a0003c0012t0001g0192a0003c0012t0001g0193a0003c0012t0003g0039others(1): Show | 4 | HG02818.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.19828-1159C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812386 | ||||||
| chr2:185812564
|
C | T | 1 | a0059c0078t0001g0289 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.19828-981C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812564 | ||||||
| chr2:185812749
|
T | A | 1 | a0006c0006t0001g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19828-796T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812749 | ||||||
| chr2:185812849
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.19828-696C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812849 | ||||||
| chr2:185812928
|
T | G | 1 | a0008c0010t0002g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19828-617T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185812928 | ||||||
| chr2:185813500
|
G | T | 1 | a0001c0001t0002g0157 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.19828-45G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | chr2 | 185813500 | ||||||
| chr2:185813514
|
A | AT | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.19828-27dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 185813514 | |||||
| chr2:185814150
|
A | G | 22 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0067others(19): Show | 25 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.20325+108A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814150 | ||||||
| chr2:185814160
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20325+118T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814160 | ||||||
| chr2:185814244
|
C | T | 19 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0269others(16): Show | 21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.20325+202C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814244 | ||||||
| chr2:185814317
|
A | G | 27 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(24): Show | 31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.20325+275A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814317 | ||||||
| chr2:185814627
|
T | C | 1 | a0001c0001t0002g0159 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.20325+585T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814627 | ||||||
| chr2:185814795
|
A | C | 1 | a0007c0007t0001g0054 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.20326-576A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814795 | ||||||
| chr2:185814983
|
G | A | 100 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.20326-388G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185814983 | ||||||
| chr2:185815120
|
T | C | 1 | a0005c0005t0001g0301 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.20326-251T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185815120 | ||||||
| chr2:185815215
|
C | G | 34 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(31): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.20326-156C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185815215 | ||||||
| chr2:185815298
|
C | CA | 4 | a0003c0012t0001g0192a0003c0012t0001g0193a0003c0012t0003g0039others(1): Show | 4 | HG02818.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.20326-67dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr2 | 185815298 | |||||
| chr2:185815314
|
G | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20326-57G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 18/22 | chr2 | 185815314 | ||||||
| chr2:185815702
|
A | C | 162 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(159): Show | 189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.20426+231A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185815702 | ||||||
| chr2:185815702
|
A | T | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20426+231A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185815702 | ||||||
| chr2:185815934
|
A | G | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.20426+463A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185815934 | ||||||
| chr2:185816171
|
A | G | 3 | a0022c0025t0001g0022a0022c0025t0001g0188a0033c0035t0001g0042 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.20426+700A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816171 | ||||||
| chr2:185816200
|
ATT | A | 162 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(159): Show | 189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.20426+740_20426+74 others(6): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816200 | |||||
| chr2:185816234
|
A | AT | 30 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(27): Show | 35 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.20426+773dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816234 | |||||
| chr2:185816560
|
G | T | 3 | a0006c0006t0001g0030a0006c0006t0001g0270a0049c0070t0001g0271 | 4 | HG02055.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.20426+1089G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816560 | ||||||
| chr2:185816585
|
C | T | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20426+1114C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816585 | ||||||
| chr2:185816596
|
G | T | 1 | a0002c0002t0001g0263 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.20426+1125G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816596 | ||||||
| chr2:185816614
|
G | T | 2 | a0003c0003t0001g0267a0003c0003t0001g0269 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.20426+1143G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816614 | ||||||
| chr2:185816663
|
C | A | 1 | a0002c0002t0001g0009 | 3 | NA18949.hp2 NA18964.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.20426+1192C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816663 | ||||||
| chr2:185816724
|
C | T | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20426+1253C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185816724 | ||||||
| chr2:185816855
|
C | CAG | 7 | a0016c0022t0002g0179a0016c0022t0002g0180a0016c0022t0002g0182others(4): Show | 8 | HG01891.hp1 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.20426+1408_20426+1 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816855 | |||||
| chr2:185816855
|
CAG | C | 248 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(245): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.20426+1408_20426+1 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816855 | |||||
| chr2:185816855
|
CAGAGAG | C | 6 | a0013c0013t0002g0130a0018c0021t0001g0023a0018c0021t0001g0197others(3): Show | 7 | HG01978.hp2 HG02717.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.20426+1404_20426+1 others(12): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816855 | |||||
| chr2:185816902
|
AAG | A | 3 | a0020c0020t0003g0013a0020c0020t0003g0062a0020c0020t0003g0063 | 4 | HG01891.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.20426+1439_20426+1 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816902 | |||||
| chr2:185816976
|
AAAG | A | 153 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(150): Show | 179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.20426+1508_20426+1 others(9): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185816976 | |||||
| chr2:185817007
|
GA | G | 92 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(89): Show | 108 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.20426+1537delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817007 | ||||||
| chr2:185817209
|
C | A | 1 | a0001c0023t0002g0136 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.20426+1738C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817209 | ||||||
| chr2:185817246
|
G | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20426+1775G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817246 | ||||||
| chr2:185817563
|
G | C | 146 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(143): Show | 172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.20426+2092G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817563 | ||||||
| chr2:185817825
|
A | G | 1 | a0017c0019t0001g0202 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.20426+2354A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817825 | ||||||
| chr2:185817851
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20426+2380C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817851 | ||||||
| chr2:185817966
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20426+2495C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817966 | ||||||
| chr2:185817975
|
T | G | 1 | a0004c0004t0004g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.20426+2504T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185817975 | ||||||
| chr2:185818049
|
A | C | 1 | a0005c0005t0001g0304 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.20426+2578A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818049 | ||||||
| chr2:185818108
|
T | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20426+2637T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818108 | ||||||
| chr2:185818143
|
A | G | 2 | a0003c0003t0001g0267a0003c0003t0001g0269 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.20426+2672A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818143 | ||||||
| chr2:185818268
|
G | A | 1 | a0003c0003t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.20426+2797G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818268 | ||||||
| chr2:185818315
|
A | G | 3 | a0018c0021t0001g0023a0018c0021t0001g0197a0018c0021t0001g0198 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.20426+2844A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818315 | ||||||
| chr2:185818702
|
A | T | 1 | a0043c0036t0001g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.20426+3231A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818702 | ||||||
| chr2:185818744
|
G | A | 55 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(52): Show | 68 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.20426+3273G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818744 | ||||||
| chr2:185818770
|
A | G | 3 | a0018c0021t0001g0023a0018c0021t0001g0197a0018c0021t0001g0198 | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.20426+3299A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818770 | ||||||
| chr2:185818796
|
G | C | 4 | a0003c0003t0001g0225a0003c0003t0001g0227a0003c0003t0001g0228others(1): Show | 4 | HG00642.hp2 HG01106.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.20426+3325G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185818796 | ||||||
| chr2:185819088
|
A | T | 4 | a0007c0007t0001g0051a0007c0007t0001g0052a0007c0007t0001g0053others(1): Show | 4 | HG01346.hp2 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.20426+3617A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185819088 | ||||||
| chr2:185819393
|
T | C | 100 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.20426+3922T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185819393 | ||||||
| chr2:185819466
|
G | C | 1 | a0003c0003t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.20426+3995G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185819466 | ||||||
| chr2:185819481
|
G | A | 27 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(24): Show | 31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.20426+4010G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185819481 | ||||||
| chr2:185819624
|
TG | T | 100 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.20426+4154delG | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185819624 | ||||||
| chr2:185819640
|
A | C | 1 | a0001c0051t0002g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.20426+4169A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185819640 | ||||||
| chr2:185819641
|
A | AT | 5 | a0006c0006t0001g0031a0006c0006t0001g0273a0006c0006t0001g0274others(2): Show | 6 | HG01099.hp1 HG02572.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.20426+4177dupT | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185819641 | |||||
| chr2:185819838
|
GTATGA | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20426+4371_20426+4 others(11): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185819838 | |||||
| chr2:185820316
|
G | T | 1 | a0003c0003t0001g0310 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.20427-4118G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820316 | ||||||
| chr2:185820345
|
C | T | 1 | a0003c0003t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.20427-4089C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820345 | ||||||
| chr2:185820463
|
CCTAT | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20427-3962_20427-3 others(10): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185820463 | |||||
| chr2:185820485
|
A | G | 1 | a0038c0052t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.20427-3949A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820485 | ||||||
| chr2:185820599
|
T | C | 3 | a0010c0011t0002g0099a0010c0011t0002g0117a0010c0047t0002g0115 | 3 | HG02738.hp1 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.20427-3835T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820599 | ||||||
| chr2:185820834
|
A | C | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.20427-3600A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820834 | ||||||
| chr2:185820939
|
A | T | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20427-3495A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820939 | ||||||
| chr2:185820967
|
A | G | 1 | a0004c0004t0001g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.20427-3467A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185820967 | ||||||
| chr2:185821009
|
TA | T | 41 | a0001c0001t0002g0108a0001c0001t0002g0113a0001c0001t0002g0114others(38): Show | 47 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.20427-3396delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | |||||
| chr2:185821009
|
TAA | T | 15 | a0001c0001t0002g0089a0001c0001t0002g0124a0001c0001t0002g0135others(12): Show | 15 | HG01106.hp2 HG01175.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.20427-3397_20427-3 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | |||||
| chr2:185821009
|
TAAA | T | 72 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(69): Show | 86 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.20427-3398_20427-3 others(9): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | |||||
| chr2:185821009
|
TAAAA | T | 8 | a0001c0001t0002g0154a0001c0001t0002g0156a0001c0001t0002g0159others(5): Show | 9 | HG01070.hp1 HG02257.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.20427-3399_20427-3 others(10): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | |||||
| chr2:185821009
|
TAAAAA | T | 8 | a0002c0002t0001g0006a0002c0002t0001g0084a0002c0002t0001g0085others(5): Show | 8 | HG01361.hp1 HG02109.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.20427-3400_20427-3 others(11): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | |||||
| chr2:185821009
|
TAAAAAA | T | 22 | a0002c0002t0001g0009a0002c0002t0001g0026a0002c0057t0001g0250others(19): Show | 26 | HG00639.hp2 HG00735.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.20427-3401_20427-3 others(12): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | |||||
| chr2:185821009
|
TAAAAAAA | T | 65 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0028others(62): Show | 78 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.20427-3402_20427-3 others(13): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | |||||
| chr2:185821009
|
TAAAAAAA others(1): Show |
T | 34 | a0002c0002t0001g0249a0003c0012t0001g0190a0003c0075t0001g0189others(31): Show | 41 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.20427-3403_20427-3 others(14): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | |||||
| chr2:185821009
|
TAAAAAAA others(2): Show |
T | 20 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0269others(17): Show | 21 | HG01070.hp2 HG02083.hp1 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.20427-3404_20427-3 others(15): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | |||||
| chr2:185821009
|
TAAAAAAA others(3): Show |
T | 13 | a0006c0006t0001g0030a0006c0006t0001g0031a0006c0006t0001g0268others(10): Show | 15 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.20427-3405_20427-3 others(16): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | |||||
| chr2:185821009
|
TAAAAAAA others(4): Show |
T | 1 | a0006c0006t0001g0270 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.20427-3406_20427-3 others(17): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821009 | |||||
| chr2:185821023
|
A | G | 25 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0067others(22): Show | 29 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.20427-3411A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821023 | ||||||
| chr2:185821024
|
A | G | 2 | a0004c0004t0001g0066a0004c0004t0001g0077 | 2 | HG01884.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.20427-3410A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821024 | ||||||
| chr2:185821057
|
C | T | 27 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(24): Show | 31 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.20427-3377C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821057 | ||||||
| chr2:185821082
|
A | AAAGAG | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20427-3348_20427-3 others(11): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821082 | |||||
| chr2:185821256
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20427-3178C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821256 | ||||||
| chr2:185821313
|
C | T | 2 | a0008c0027t0002g0090a0008c0027t0002g0093 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.20427-3121C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821313 | ||||||
| chr2:185821380
|
C | T | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20427-3054C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821380 | ||||||
| chr2:185821408
|
C | T | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20427-3026C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821408 | ||||||
| chr2:185821500
|
C | G | 2 | a0017c0019t0001g0024a0017c0019t0001g0217 | 3 | HG03491.hp2 HG03492.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.20427-2934C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821500 | ||||||
| chr2:185821522
|
C | T | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.20427-2912C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821522 | ||||||
| chr2:185821601
|
G | A | 1 | a0002c0018t0001g0241 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.20427-2833G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821601 | ||||||
| chr2:185821925
|
C | CA | 7 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0008t0002g0144others(4): Show | 7 | HG03540.hp1 HG04199.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.20427-2491dupA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821925 | |||||
| chr2:185821925
|
CA | C | 98 | a0001c0001t0002g0154a0001c0001t0002g0156a0003c0003t0001g0014others(95): Show | 112 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.20427-2491delA | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821925 | |||||
| chr2:185821925
|
CAA | C | 63 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(60): Show | 76 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.20427-2492_20427-2 others(8): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 185821925 | |||||
| chr2:185821933
|
A | C | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20427-2501A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821933 | ||||||
| chr2:185821941
|
A | C | 1 | a0002c0002t0001g0185 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.20427-2493A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821941 | ||||||
| chr2:185821976
|
T | C | 1 | a0004c0004t0001g0073 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.20427-2458T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821976 | ||||||
| chr2:185821986
|
G | T | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20427-2448G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185821986 | ||||||
| chr2:185822004
|
G | C | 1 | a0005c0005t0001g0301 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.20427-2430G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822004 | ||||||
| chr2:185822033
|
A | G | 1 | a0005c0005t0001g0296 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.20427-2401A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822033 | ||||||
| chr2:185822191
|
C | T | 1 | a0002c0002t0001g0233 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.20427-2243C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822191 | ||||||
| chr2:185822293
|
A | C | 2 | a0001c0001t0002g0018a0034c0050t0002g0018 | 2 | HG01081.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.20427-2141A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822293 | ||||||
| chr2:185822313
|
C | A | 1 | a0003c0003t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.20427-2121C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822313 | ||||||
| chr2:185822605
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.20427-1829G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822605 | ||||||
| chr2:185822663
|
C | A | 17 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0269others(14): Show | 19 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.20427-1771C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822663 | ||||||
| chr2:185822753
|
C | A | 1 | a0001c0001t0002g0112 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.20427-1681C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822753 | ||||||
| chr2:185822885
|
C | T | 1 | a0003c0003t0001g0199 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.20427-1549C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822885 | ||||||
| chr2:185822989
|
T | A | 1 | a0002c0002t0001g0252 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.20427-1445T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185822989 | ||||||
| chr2:185823120
|
G | T | 3 | a0003c0012t0001g0193a0003c0012t0003g0039a0003c0012t0003g0040 | 3 | HG02895.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.20427-1314G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185823120 | ||||||
| chr2:185823280
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20427-1154T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185823280 | ||||||
| chr2:185823500
|
C | T | 1 | a0002c0002t0001g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.20427-934C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185823500 | ||||||
| chr2:185823989
|
C | A | 1 | a0006c0006t0001g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.20427-445C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185823989 | ||||||
| chr2:185824158
|
G | A | 1 | a0003c0003t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.20427-276G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185824158 | ||||||
| chr2:185824217
|
A | G | 34 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0066others(31): Show | 40 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.20427-217A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185824217 | ||||||
| chr2:185824240
|
G | A | 100 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.20427-194G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185824240 | ||||||
| chr2:185824255
|
A | G | 1 | a0002c0002t0001g0248 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.20427-179A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185824255 | ||||||
| chr2:185824416
|
C | G | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20427-18C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 19/22 | chr2 | 185824416 | ||||||
| chr2:185824832
|
T | C | 153 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(150): Show | 179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.20473+352T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185824832 | ||||||
| chr2:185825016
|
G | A | 19 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0269others(16): Show | 21 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.20473+536G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185825016 | ||||||
| chr2:185825260
|
T | G | 93 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(90): Show | 109 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.20473+780T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185825260 | ||||||
| chr2:185825467
|
A | G | 1 | a0007c0007t0001g0060 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.20473+987A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185825467 | ||||||
| chr2:185825468
|
T | C | 38 | a0003c0003t0001g0014a0003c0003t0001g0025a0003c0003t0001g0199others(35): Show | 41 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.20473+988T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185825468 | ||||||
| chr2:185826007
|
A | T | 1 | a0006c0006t0001g0273 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.20473+1527A>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826007 | ||||||
| chr2:185826096
|
T | C | 1 | a0001c0001t0002g0163 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.20473+1616T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826096 | ||||||
| chr2:185826110
|
G | A | 1 | a0022c0025t0001g0022 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.20473+1630G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826110 | ||||||
| chr2:185826255
|
A | G | 1 | a0003c0012t0001g0190 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.20473+1775A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826255 | ||||||
| chr2:185826293
|
C | G | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20473+1813C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826293 | ||||||
| chr2:185826321
|
T | C | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20474-1835T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826321 | ||||||
| chr2:185826540
|
G | C | 4 | a0001c0001t0002g0089a0001c0001t0002g0152a0001c0001t0002g0171others(1): Show | 4 | HG00438.hp1 NA18959.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.20474-1616G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826540 | ||||||
| chr2:185826624
|
T | A | 163 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(160): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.20474-1532T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826624 | ||||||
| chr2:185826967
|
GGGCACCA others(3): Show |
G | 1 | a0001c0001t0002g0150 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.20474-1188_20474-1 others(16): Show |
FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185826967 | ||||||
| chr2:185827032
|
G | A | 100 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.20474-1124G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185827032 | ||||||
| chr2:185827275
|
C | G | 1 | a0036c0049t0002g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.20474-881C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185827275 | ||||||
| chr2:185827316
|
G | A | 100 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.20474-840G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185827316 | ||||||
| chr2:185827354
|
T | A | 1 | a0004c0004t0001g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.20474-802T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185827354 | ||||||
| chr2:185827922
|
C | T | 14 | a0006c0006t0001g0030a0006c0006t0001g0031a0006c0006t0001g0268others(11): Show | 16 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.20474-234C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185827922 | ||||||
| chr2:185828144
|
T | A | 1 | a0029c0039t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20474-12T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 20/22 | chr2 | 185828144 | ||||||
| chr2:185828403
|
T | C | 1 | a0001c0001t0002g0151 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.20517+204T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185828403 | ||||||
| chr2:185828863
|
A | G | 93 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(90): Show | 109 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.20517+664A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185828863 | ||||||
| chr2:185828881
|
G | A | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.20517+682G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185828881 | ||||||
| chr2:185828976
|
G | T | 1 | a0003c0003t0001g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.20517+777G>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185828976 | ||||||
| chr2:185829125
|
T | G | 1 | a0042c0077t0001g0218 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.20517+926T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185829125 | ||||||
| chr2:185829317
|
T | C | 94 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(91): Show | 110 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.20517+1118T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185829317 | ||||||
| chr2:185829394
|
A | G | 1 | a0001c0043t0002g0127 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.20517+1195A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185829394 | ||||||
| chr2:185829480
|
T | C | 2 | a0003c0003t0001g0205a0003c0003t0001g0209 | 2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.20517+1281T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185829480 | ||||||
| chr2:185829531
|
G | A | 35 | a0003c0003t0001g0014a0003c0003t0001g0025a0003c0003t0001g0199others(32): Show | 38 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.20517+1332G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185829531 | ||||||
| chr2:185829963
|
A | C | 98 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(95): Show | 113 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.20517+1764A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185829963 | ||||||
| chr2:185830095
|
A | G | 166 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(163): Show | 193 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.20518-1718A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830095 | ||||||
| chr2:185830154
|
C | A | 1 | a0004c0004t0004g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.20518-1659C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830154 | ||||||
| chr2:185830256
|
A | G | 1 | a0002c0002t0001g0009 | 3 | NA18949.hp2 NA18964.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.20518-1557A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830256 | ||||||
| chr2:185830276
|
A | G | 25 | a0005c0005t0001g0011a0005c0005t0001g0032a0005c0005t0001g0033others(22): Show | 30 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.20518-1537A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830276 | ||||||
| chr2:185830323
|
T | C | 1 | a0042c0077t0001g0218 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.20518-1490T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830323 | ||||||
| chr2:185830408
|
T | G | 1 | a0060c0079t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20518-1405T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830408 | ||||||
| chr2:185830508
|
T | C | 20 | a0003c0003t0001g0014a0003c0003t0001g0210a0003c0003t0001g0213others(17): Show | 21 | HG00639.hp2 HG00735.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.20518-1305T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830508 | ||||||
| chr2:185830669
|
A | G | 156 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(153): Show | 182 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.20518-1144A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830669 | ||||||
| chr2:185830675
|
G | A | 31 | a0003c0072t0001g0184a0004c0004t0001g0005a0004c0004t0001g0065others(28): Show | 37 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.20518-1138G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830675 | ||||||
| chr2:185830687
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.20518-1126A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185830687 | ||||||
| chr2:185831217
|
C | A | 1 | a0002c0002t0001g0257 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.20518-596C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185831217 | ||||||
| chr2:185831389
|
A | C | 3 | a0006c0006t0001g0277a0006c0006t0001g0278a0006c0006t0001g0279 | 3 | HG02280.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.20518-424A>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185831389 | ||||||
| chr2:185831531
|
C | G | 297 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(294): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.20518-282C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185831531 | ||||||
| chr2:185831642
|
C | G | 197 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(194): Show | 230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.20518-171C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185831642 | ||||||
| chr2:185831761
|
A | G | 1 | a0009c0009t0001g0294 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.20518-52A>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 21/22 | chr2 | 185831761 | ||||||
| chr2:185831979
|
C | G | 2 | a0005c0005t0001g0291a0005c0005t0001g0292 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.20587+97C>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185831979 | ||||||
| chr2:185832032
|
C | T | 197 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(194): Show | 230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.20587+150C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832032 | ||||||
| chr2:185832123
|
C | T | 18 | a0004c0004t0001g0005a0004c0004t0001g0065a0004c0004t0001g0067others(15): Show | 21 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.20587+241C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832123 | ||||||
| chr2:185832132
|
T | C | 1 | a0023c0028t0001g0302 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.20587+250T>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832132 | ||||||
| chr2:185832244
|
G | A | 1 | a0013c0013t0002g0147 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.20587+362G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832244 | ||||||
| chr2:185832370
|
G | C | 2 | a0001c0001t0002g0118a0001c0001t0002g0126 | 2 | HG00423.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.20587+488G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832370 | ||||||
| chr2:185832656
|
G | A | 3 | a0022c0025t0001g0022a0022c0025t0001g0188a0033c0035t0001g0042 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.20588-434G>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832656 | ||||||
| chr2:185832667
|
G | C | 197 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0009others(194): Show | 230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.20588-423G>C | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832667 | ||||||
| chr2:185832672
|
T | A | 3 | a0006c0006t0001g0277a0006c0006t0001g0278a0006c0006t0001g0279 | 3 | HG02280.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.20588-418T>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832672 | ||||||
| chr2:185832768
|
T | G | 23 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0269others(20): Show | 25 | HG01099.hp1 HG02055.hp2 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.20588-322T>G | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832768 | ||||||
| chr2:185832961
|
C | A | 6 | a0013c0013t0002g0121a0013c0013t0002g0130a0013c0013t0002g0140others(3): Show | 6 | HG01109.hp2 HG01168.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.20588-129C>A | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832961 | ||||||
| chr2:185832983
|
C | T | 9 | a0006c0006t0001g0031a0006c0006t0001g0273a0006c0006t0001g0274others(6): Show | 10 | HG01099.hp1 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.20588-107C>T | FSIP2 | ENSG00000188738.16 | transcript | ENST00000424728.6 | protein_coding | 22/22 | chr2 | 185832983 |