Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6709 |
|---|---|
| ensemblid | ENSG00000197694.19 |
| hgncid | 11273 |
| symbol | SPTAN1 |
| name | spectrin alpha, non-erythrocytic 1 |
| refseq_nuc | NM_001130438.3 |
| refseq_prot | NP_001123910.1 |
| ensembl_nuc | ENST00000372739.7 |
| ensembl_prot | ENSP00000361824.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 128552587 |
| end | 128633662 |
| strand | + |
| ver | v1.2 |
| region | chr9:128552587-128633662 |
| region5000 | chr9:128547587-128638662 |
| regionname0 | SPTAN1_chr9_128552587_128633662 |
| regionname5000 | SPTAN1_chr9_128547587_128638662 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2477 | 294 | 83 | 38 | 133 | 12 | 26 | 104 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0002 | 0/0 | 2477 | 11 | 0 | 0 | 9 | 0 | 2 | 8 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0003 | 0/0 | 2477 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0004 | 0/0 | 2477 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0005 | 0/0 | 2477 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0006 | 0/0 | 2477 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 7434 | 119 | 25 | 17 | 52 | 10 | 14 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0002 | 0/0 | 7434 | 104 | 19 | 11 | 61 | 2 | 11 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0003 | 0/0 | 7434 | 13 | 0 | 0 | 13 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0004 | 0/0 | 7434 | 11 | 0 | 0 | 9 | 0 | 2 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0005 | 1/0 | 7434 | 9 | 8 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0006 | 0/0 | 7434 | 8 | 6 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0007 | 0/0 | 7434 | 7 | 7 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0008 | 0/0 | 7434 | 6 | 4 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0009 | 0/0 | 7434 | 3 | 3 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0010 | 0/0 | 7434 | 3 | 3 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0011 | 0/0 | 7434 | 3 | 0 | 0 | 3 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0012 | 0/0 | 7434 | 3 | 0 | 3 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0013 | 0/0 | 7434 | 3 | 0 | 0 | 3 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0014 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0015 | 0/0 | 7434 | 2 | 0 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0016 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0017 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0018 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0019 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0020 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0021 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0022 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0023 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0024 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0025 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0026 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0027 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0028 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0029 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0030 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| c0031 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| 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 | 1/1 | 442 | 295 | 81 | 39 | 136 | 12 | 25 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| t0002 | 0/0 | 442 | 10 | 0 | 0 | 8 | 0 | 2 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| t0003 | 0/0 | 442 | 2 | 2 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| t0004 | 0/0 | 442 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| t0005 | 0/0 | 442 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| t0006 | 0/0 | 442 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| t0007 | 0/0 | 442 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| t0008 | 0/0 | 442 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0021 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 7434 | 119 | 25 | 17 | 52 | 10 | 14 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0002 | 0/0 | 7434 | 104 | 19 | 11 | 61 | 2 | 11 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0003 | 0/0 | 7434 | 13 | 0 | 0 | 13 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0005 | 1/0 | 7434 | 9 | 8 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0006 | 0/0 | 7434 | 8 | 6 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0007 | 0/0 | 7434 | 7 | 7 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0008 | 0/0 | 7434 | 6 | 4 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0009 | 0/0 | 7434 | 3 | 3 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0010 | 0/0 | 7434 | 3 | 3 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0012 | 0/0 | 7434 | 3 | 0 | 3 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0013 | 0/0 | 7434 | 3 | 0 | 0 | 3 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0014 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0016 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0017 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0018 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0019 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0021 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0022 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0023 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0024 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0025 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0026 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0027 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0028 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0029 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0030 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0002c0004 | 0/0 | 7434 | 11 | 0 | 0 | 9 | 0 | 2 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0003c0011 | 0/0 | 7434 | 3 | 0 | 0 | 3 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0004c0015 | 0/0 | 7434 | 2 | 0 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0005c0020 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0006c0031 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7875 | 117 | 25 | 17 | 50 | 10 | 14 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0001t0007 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0001t0008 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0002t0001 | 0/0 | 7875 | 103 | 19 | 11 | 61 | 2 | 10 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0002t0005 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0003t0001 | 0/0 | 7875 | 13 | 0 | 0 | 13 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0005t0001 | 1/0 | 7875 | 9 | 8 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0006t0001 | 0/0 | 7875 | 8 | 6 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0007t0001 | 0/0 | 7875 | 7 | 7 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0008t0001 | 0/0 | 7875 | 6 | 4 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0009t0001 | 0/0 | 7875 | 3 | 3 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0010t0001 | 0/0 | 7875 | 3 | 3 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0012t0001 | 0/0 | 7875 | 3 | 0 | 3 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0013t0001 | 0/0 | 7875 | 3 | 0 | 0 | 3 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0014t0003 | 0/0 | 7875 | 2 | 2 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0016t0001 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0017t0006 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0018t0004 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0019t0001 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0021t0001 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0022t0001 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0023t0001 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0024t0001 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0025t0001 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0026t0001 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0027t0001 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0028t0001 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0029t0001 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0001c0030t0001 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0002c0004t0001 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0002c0004t0002 | 0/0 | 7875 | 10 | 0 | 0 | 8 | 0 | 2 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0003c0011t0001 | 0/0 | 7875 | 3 | 0 | 0 | 3 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0004c0015t0001 | 0/0 | 7875 | 2 | 0 | 2 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0005c0020t0001 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| a0006c0031t0001 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | copy fasta | chr9 | 128547587 | 128638662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0002t0005g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0021 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0006t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0007t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0008t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0008t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0008t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0008t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0008t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0008t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0009t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0009t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0009t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0010t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0010t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0010t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0012t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0012t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0012t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0013t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0013t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0013t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0014t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0014t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0016t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0017t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0018t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0019t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0021t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0022t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0023t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0024t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0025t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0026t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0027t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0028t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0029t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0001c0030t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0002c0004t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0003c0011t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0003c0011t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0003c0011t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0004c0015t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0004c0015t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0005c0020t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| a0006c0031t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | GBR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | FIN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0246 | EUR | FIN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0127 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00609 | hp2 | a0001 | c0027 | t0001 | g0113 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0123 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00735 | hp2 | a0001 | c0012 | t0001 | g0120 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01069 | hp1 | a0001 | c0006 | t0001 | g0297 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01069 | hp2 | a0001 | c0030 | t0001 | g0287 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01099 | hp2 | a0001 | c0008 | t0001 | g0167 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01109 | hp2 | a0001 | c0017 | t0006 | g0012 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01167 | hp2 | a0001 | c0006 | t0001 | g0292 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01256 | hp2 | a0004 | c0015 | t0001 | g0173 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01257 | hp2 | a0001 | c0012 | t0001 | g0109 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01258 | hp1 | a0004 | c0015 | t0001 | g0182 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01258 | hp2 | a0001 | c0012 | t0001 | g0110 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01496 | hp2 | a0001 | c0008 | t0001 | g0170 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0288 | EUR | IBS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01884 | hp1 | a0001 | c0007 | t0001 | g0008 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01891 | hp2 | a0001 | c0009 | t0001 | g0026 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01978 | hp2 | a0001 | c0029 | t0001 | g0077 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0214 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02040 | hp1 | a0001 | c0024 | t0001 | g0191 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02040 | hp2 | a0002 | c0004 | t0002 | g0281 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0261 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0015 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0124 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | KHV | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02145 | hp2 | a0001 | c0006 | t0001 | g0294 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | CDX | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02258 | hp1 | a0001 | c0008 | t0001 | g0171 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02280 | hp1 | a0001 | c0008 | t0001 | g0168 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02280 | hp2 | a0001 | c0007 | t0001 | g0009 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0258 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02451 | hp1 | a0001 | c0006 | t0001 | g0296 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0202 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02572 | hp1 | a0001 | c0023 | t0001 | g0306 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02615 | hp1 | a0001 | c0010 | t0001 | g0300 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02615 | hp2 | a0001 | c0007 | t0001 | g0273 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0256 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02717 | hp1 | a0001 | c0021 | t0001 | g0307 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02717 | hp2 | a0001 | c0007 | t0001 | g0274 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0014 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02809 | hp1 | a0001 | c0010 | t0001 | g0301 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0016 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0305 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02922 | hp1 | a0001 | c0007 | t0001 | g0045 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02922 | hp2 | a0001 | c0016 | t0001 | g0024 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02965 | hp2 | a0001 | c0008 | t0001 | g0169 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02970 | hp2 | a0001 | c0006 | t0001 | g0295 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03098 | hp1 | a0001 | c0007 | t0001 | g0007 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0308 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03139 | hp1 | a0001 | c0006 | t0001 | g0293 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03139 | hp2 | a0005 | c0020 | t0001 | g0006 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0222 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03209 | hp1 | a0001 | c0014 | t0003 | g0019 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03209 | hp2 | a0001 | c0007 | t0001 | g0272 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0298 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0227 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03516 | hp1 | a0001 | c0005 | t0001 | g0013 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03516 | hp2 | a0001 | c0009 | t0001 | g0004 | AFR | ESN | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03540 | hp1 | a0001 | c0010 | t0001 | g0302 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0221 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03579 | hp2 | a0001 | c0009 | t0001 | g0025 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0212 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03669 | hp2 | a0002 | c0004 | t0002 | g0276 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03688 | hp1 | a0002 | c0004 | t0002 | g0275 | SAS | STU | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0257 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0208 | SAS | BEB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0206 | SAS | BEB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0270 | SAS | BEB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG04184 | hp2 | a0001 | c0026 | t0001 | g0198 | SAS | BEB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0252 | SAS | STU | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0233 | SAS | STU | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0232 | SAS | STU | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0188 | AFR | YRI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | YRI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18906 | hp2 | a0001 | c0008 | t0001 | g0172 | AFR | YRI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0089 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0108 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18949 | hp1 | a0002 | c0004 | t0002 | g0282 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18960 | hp1 | a0001 | c0001 | t0007 | g0061 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18968 | hp1 | a0002 | c0004 | t0002 | g0278 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18975 | hp2 | a0002 | c0004 | t0002 | g0284 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18980 | hp1 | a0003 | c0011 | t0001 | g0060 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18985 | hp2 | a0001 | c0013 | t0001 | g0164 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18986 | hp1 | a0001 | c0013 | t0001 | g0160 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18989 | hp1 | a0001 | c0013 | t0001 | g0163 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0135 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18998 | hp1 | a0002 | c0004 | t0002 | g0280 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18998 | hp2 | a0003 | c0011 | t0001 | g0057 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18999 | hp1 | a0002 | c0004 | t0002 | g0283 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18999 | hp2 | a0006 | c0031 | t0001 | g0243 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19009 | hp1 | a0003 | c0011 | t0001 | g0059 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | LWK | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0022 | AFR | LWK | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19043 | hp2 | a0001 | c0025 | t0001 | g0179 | AFR | LWK | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19057 | hp2 | a0002 | c0004 | t0002 | g0277 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19063 | hp1 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19081 | hp1 | a0002 | c0004 | t0002 | g0279 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19081 | hp2 | a0001 | c0019 | t0001 | g0205 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19086 | hp1 | a0002 | c0004 | t0001 | g0285 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19089 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19090 | hp2 | a0001 | c0028 | t0001 | g0159 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | YRI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0254 | EUR | TSI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0017 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0219 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0020 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02486 | hp2 | a0001 | c0022 | t0001 | g0262 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02559 | hp1 | a0001 | c0014 | t0003 | g0018 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG02559 | hp2 | a0001 | c0006 | t0001 | g0299 | AFR | ACB | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0023 | AFR | MSL | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | USA | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | USA | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| NA21309 | hp2 | a0001 | c0018 | t0004 | g0189 | AFR | LWK | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0099 | REF | REF | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| homoSapiens_grch38 | hp1 | a0001 | c0005 | t0001 | g0021 | REF | REF | SPTAN1_chr9_128547587_128638662 | SPTAN1 | chr9 | 128547587 | 128638662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:128577394
|
C | T | 1 | a0006 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.973C>T | p.His325Tyr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 8/57 | 1086/7875 | 973/7434 | 325/2477 | chr9 | 128577394 | ||
| chr9:128580928
|
G | A | 1 | a0002 | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
missense_variant | MODERATE | c.1330G>A | p.Val444Ile | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/57 | 1443/7875 | 1330/7434 | 444/2477 | chr9 | 128580928 | ||
| chr9:128608922
|
G | A | 1 | a0003 | 3 | NA18980.hp1 NA18998.hp2 NA19009.hp1 |
missense_variant | MODERATE | c.4540G>A | p.Ala1514Thr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 35/57 | 4653/7875 | 4540/7434 | 1514/2477 | chr9 | 128608922 | ||
| chr9:128618060
|
C | T | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.5552C>T | p.Ala1851Val | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/57 | 5665/7875 | 5552/7434 | 1851/2477 | chr9 | 128618060 | ||
| chr9:128632128
|
G | A | 1 | a0004 | 2 | HG01256.hp2 HG01258.hp1 |
missense_variant&splice_region_variant | MODERATE | c.6764G>A | p.Arg2255His | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 53/57 | 6877/7875 | 6764/7434 | 2255/2477 | chr9 | 128632128 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:128583939
|
A | C | 26 | a0001c0001a0001c0002a0001c0003others(23): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
synonymous_variant | LOW | c.2163A>C | p.Ala721Ala | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 16/57 | 2276/7875 | 2163/7434 | 721/2477 | chr9 | 128583939 | ||
| chr9:128584431
|
C | A | 2 | a0001c0006a0001c0010 | 11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
synonymous_variant | LOW | c.2343C>A | p.Ala781Ala | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 17/57 | 2456/7875 | 2343/7434 | 781/2477 | chr9 | 128584431 | ||
| chr9:128588817
|
G | A | 1 | a0001c0018 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.2880G>A | p.Val960Val | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/57 | 2993/7875 | 2880/7434 | 960/2477 | chr9 | 128588817 | ||
| chr9:128591521
|
G | A | 1 | a0001c0019 | 1 | NA19081.hp2 | synonymous_variant | LOW | c.3051G>A | p.Pro1017Pro | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/57 | 3164/7875 | 3051/7434 | 1017/2477 | chr9 | 128591521 | ||
| chr9:128594259
|
G | A | 1 | a0001c0006 | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
synonymous_variant | LOW | c.3300G>A | p.Ala1100Ala | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/57 | 3413/7875 | 3300/7434 | 1100/2477 | chr9 | 128594259 | ||
| chr9:128598471
|
C | T | 10 | a0001c0001a0001c0003a0001c0008others(7): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
synonymous_variant | LOW | c.3486C>T | p.Leu1162Leu | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 25/57 | 3599/7875 | 3486/7434 | 1162/2477 | chr9 | 128598471 | ||
| chr9:128600082
|
T | C | 2 | a0001c0007a0005c0020 | 8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
splice_region_variant&synonymous_variant | LOW | c.3546T>C | p.Asp1182Asp | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/57 | 3659/7875 | 3546/7434 | 1182/2477 | chr9 | 128600082 | ||
| chr9:128605076
|
A | G | 1 | a0001c0026 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.3762A>G | p.Gln1254Gln | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 30/57 | 3875/7875 | 3762/7434 | 1254/2477 | chr9 | 128605076 | ||
| chr9:128608195
|
C | T | 1 | a0001c0009 | 3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.4410C>T | p.Thr1470Thr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/57 | 4523/7875 | 4410/7434 | 1470/2477 | chr9 | 128608195 | ||
| chr9:128608924
|
C | T | 1 | a0001c0025 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.4542C>T | p.Ala1514Ala | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 35/57 | 4655/7875 | 4542/7434 | 1514/2477 | chr9 | 128608924 | ||
| chr9:128612222
|
G | A | 1 | a0001c0016 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.5019G>A | p.Lys1673Lys | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/57 | 5132/7875 | 5019/7434 | 1673/2477 | chr9 | 128612222 | ||
| chr9:128613422
|
A | G | 29 | a0001c0001a0001c0002a0001c0003others(26): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
synonymous_variant | LOW | c.5085A>G | p.Leu1695Leu | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/57 | 5198/7875 | 5085/7434 | 1695/2477 | chr9 | 128613422 | ||
| chr9:128613443
|
G | A | 1 | a0001c0021 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.5106G>A | p.Leu1702Leu | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/57 | 5219/7875 | 5106/7434 | 1702/2477 | chr9 | 128613443 | ||
| chr9:128615784
|
A | G | 1 | a0001c0030 | 1 | HG01069.hp2 | synonymous_variant | LOW | c.5301A>G | p.Glu1767Glu | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/57 | 5414/7875 | 5301/7434 | 1767/2477 | chr9 | 128615784 | ||
| chr9:128617688
|
C | T | 9 | a0001c0001a0001c0003a0001c0012others(6): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
synonymous_variant | LOW | c.5406C>T | p.Thr1802Thr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/57 | 5519/7875 | 5406/7434 | 1802/2477 | chr9 | 128617688 | ||
| chr9:128617719
|
C | A | 2 | a0001c0003a0001c0024 | 14 | HG00408.hp1 HG00621.hp1 HG02040.hp1 others(11): Show |
synonymous_variant | LOW | c.5437C>A | p.Arg1813Arg | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/57 | 5550/7875 | 5437/7434 | 1813/2477 | chr9 | 128617719 | ||
| chr9:128618031
|
C | T | 1 | a0001c0013 | 3 | NA18985.hp2 NA18986.hp1 NA18989.hp1 |
synonymous_variant | LOW | c.5523C>T | p.Ile1841Ile | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/57 | 5636/7875 | 5523/7434 | 1841/2477 | chr9 | 128618031 | ||
| chr9:128618052
|
G | A | 1 | a0001c0028 | 1 | NA19090.hp2 | synonymous_variant | LOW | c.5544G>A | p.Gln1848Gln | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/57 | 5657/7875 | 5544/7434 | 1848/2477 | chr9 | 128618052 | ||
| chr9:128621199
|
C | T | 1 | a0001c0012 | 3 | HG00735.hp2 HG01257.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.5775C>T | p.Thr1925Thr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/57 | 5888/7875 | 5775/7434 | 1925/2477 | chr9 | 128621199 | ||
| chr9:128621214
|
C | T | 1 | a0001c0023 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.5790C>T | p.Arg1930Arg | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/57 | 5903/7875 | 5790/7434 | 1930/2477 | chr9 | 128621214 | ||
| chr9:128624420
|
G | A | 2 | a0001c0009a0001c0016 | 4 | HG01891.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
synonymous_variant | LOW | c.5925G>A | p.Ala1975Ala | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 46/57 | 6038/7875 | 5925/7434 | 1975/2477 | chr9 | 128624420 | ||
| chr9:128626660
|
C | A | 1 | a0001c0009 | 3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.6549C>A | p.Thr2183Thr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/57 | 6662/7875 | 6549/7434 | 2183/2477 | chr9 | 128626660 | ||
| chr9:128627463
|
C | T | 1 | a0001c0022 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.6654C>T | p.His2218His | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 50/57 | 6767/7875 | 6654/7434 | 2218/2477 | chr9 | 128627463 | ||
| chr9:128627469
|
C | T | 1 | a0001c0010 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.6660C>T | p.Asn2220Asn | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 50/57 | 6773/7875 | 6660/7434 | 2220/2477 | chr9 | 128627469 | ||
| chr9:128632626
|
C | T | 1 | a0001c0029 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.7068C>T | p.Cys2356Cys | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 55/57 | 7181/7875 | 7068/7434 | 2356/2477 | chr9 | 128632626 | ||
| chr9:128633289
|
C | T | 1 | a0001c0008 | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
synonymous_variant | LOW | c.7389C>T | p.Thr2463Thr | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 7502/7875 | 7389/7434 | 2463/2477 | chr9 | 128633289 | ||
| chr9:128633292
|
G | A | 1 | a0001c0017 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.7392G>A | p.Ala2464Ala | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 7505/7875 | 7392/7434 | 2464/2477 | chr9 | 128633292 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:128633393
|
C | T | 1 | a0001c0001t0008 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*59C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 59 | chr9 | 128633393 | |||||
| chr9:128633445
|
G | T | 1 | a0002c0004t0002 | 10 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*111G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 111 | chr9 | 128633445 | |||||
| chr9:128633482
|
C | T | 1 | a0001c0014t0003 | 2 | HG02559.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*148C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 148 | chr9 | 128633482 | |||||
| chr9:128633483
|
G | A | 1 | a0001c0018t0004 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 149 | chr9 | 128633483 | |||||
| chr9:128633489
|
G | A | 2 | a0001c0002t0005a0001c0017t0006 | 2 | HG01109.hp2 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*155G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 155 | chr9 | 128633489 | |||||
| chr9:128633633
|
A | G | 1 | a0001c0001t0007 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*299A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 299 | chr9 | 128633633 | |||||
| chr9:128633658
|
C | G | 1 | a0001c0017t0006 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*324C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 57/57 | 324 | chr9 | 128633658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:128552743
|
C | G | 4 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(1): Show | 4 | NA18948.hp1 NA18960.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+47C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128552743 | ||||||
| chr9:128552752
|
C | G | 4 | a0001c0002t0001g0305a0001c0002t0001g0308a0001c0021t0001g0307others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+56C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128552752 | ||||||
| chr9:128552759
|
G | C | 3 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003 | 3 | NA18972.hp2 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-4+63G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128552759 | ||||||
| chr9:128552821
|
C | A | 1 | a0001c0009t0001g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-4+125C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128552821 | ||||||
| chr9:128552976
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-4+280C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128552976 | ||||||
| chr9:128553103
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-4+407G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553103 | ||||||
| chr9:128553239
|
C | T | 12 | a0001c0001t0001g0303a0001c0006t0001g0292a0001c0006t0001g0293others(9): Show | 12 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4+543C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553239 | ||||||
| chr9:128553291
|
G | A | 6 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0007t0001g0007others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+595G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553291 | ||||||
| chr9:128553320
|
C | G | 1 | a0001c0002t0001g0291 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-4+624C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553320 | ||||||
| chr9:128553401
|
ATAACT | A | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-4+709_-4+713delCT others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128553401 | |||||
| chr9:128553658
|
A | G | 12 | a0001c0001t0001g0303a0001c0006t0001g0292a0001c0006t0001g0293others(9): Show | 12 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4+962A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553658 | ||||||
| chr9:128553787
|
C | G | 3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG00280.hp1 HG01515.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-4+1091C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553787 | ||||||
| chr9:128553805
|
C | T | 1 | a0001c0030t0001g0287 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-4+1109C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553805 | ||||||
| chr9:128553847
|
G | A | 1 | a0001c0017t0006g0012 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-4+1151G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553847 | ||||||
| chr9:128553878
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-4+1182G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553878 | ||||||
| chr9:128553962
|
A | G | 4 | a0001c0001t0001g0303a0001c0010t0001g0300a0001c0010t0001g0301others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+1266A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128553962 | ||||||
| chr9:128554002
|
G | A | 6 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0007t0001g0007others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+1306G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554002 | ||||||
| chr9:128554004
|
C | A | 1 | a0001c0003t0001g0028 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-4+1308C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554004 | ||||||
| chr9:128554107
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-4+1411A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554107 | ||||||
| chr9:128554338
|
A | G | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4+1642A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554338 | ||||||
| chr9:128554453
|
C | A | 4 | a0001c0001t0001g0303a0001c0010t0001g0300a0001c0010t0001g0301others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+1757C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554453 | ||||||
| chr9:128554586
|
A | C | 2 | a0001c0007t0001g0273a0001c0007t0001g0274 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-4+1890A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554586 | ||||||
| chr9:128554597
|
C | G | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-4+1901C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554597 | ||||||
| chr9:128554668
|
G | A | 1 | a0001c0003t0001g0029 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-4+1972G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554668 | ||||||
| chr9:128554768
|
C | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-4+2072C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128554768 | ||||||
| chr9:128555054
|
T | C | 1 | a0005c0020t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-4+2358T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555054 | ||||||
| chr9:128555076
|
G | A | 5 | a0001c0005t0001g0013a0001c0005t0001g0014a0001c0005t0001g0015others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+2380G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555076 | ||||||
| chr9:128555122
|
C | G | 116 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(113): Show | 116 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-4+2426C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555122 | ||||||
| chr9:128555583
|
A | G | 7 | a0001c0007t0001g0272a0001c0008t0001g0167a0001c0008t0001g0168others(4): Show | 7 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+2887A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555583 | ||||||
| chr9:128555620
|
CT | C | 114 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(111): Show | 114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-4+2947delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128555620 | |||||
| chr9:128555620
|
CTT | C | 7 | a0001c0002t0001g0174a0001c0002t0001g0175a0001c0002t0001g0176others(4): Show | 7 | HG01256.hp2 HG02083.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+2946_-4+2947del others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128555620 | |||||
| chr9:128555621
|
T | TTCC | 10 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0161others(7): Show | 10 | HG02135.hp1 HG02300.hp2 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4+2926_-4+2927ins others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128555621 | |||||
| chr9:128555622
|
T | TC | 37 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(34): Show | 37 | HG00099.hp2 HG01099.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4+2926_-4+2927ins others(1): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555622 | ||||||
| chr9:128555622
|
T | TCC | 123 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0046others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.-4+2926_-4+2927ins others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555622 | ||||||
| chr9:128555623
|
T | C | 51 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(48): Show | 51 | HG00099.hp2 HG01069.hp1 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.-4+2927T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555623 | ||||||
| chr9:128555624
|
T | C | 123 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(120): Show | 123 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-4+2928T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555624 | ||||||
| chr9:128555625
|
T | C | 116 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(113): Show | 116 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-4+2929T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555625 | ||||||
| chr9:128555626
|
T | C | 7 | a0001c0002t0001g0174a0001c0002t0001g0175a0001c0002t0001g0176others(4): Show | 7 | HG01256.hp2 HG02083.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+2930T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555626 | ||||||
| chr9:128555792
|
G | A | 298 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-4+3096G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128555792 | ||||||
| chr9:128556039
|
G | C | 2 | a0001c0014t0003g0018a0001c0014t0003g0019 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-4+3343G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556039 | ||||||
| chr9:128556057
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-4+3361T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556057 | ||||||
| chr9:128556286
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-4+3590G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556286 | ||||||
| chr9:128556288
|
C | T | 8 | a0002c0004t0001g0285a0002c0004t0002g0278a0002c0004t0002g0279others(5): Show | 8 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4+3592C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556288 | ||||||
| chr9:128556299
|
C | CA | 4 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 4 | HG02074.hp2 NA18984.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+3604dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128556299 | |||||
| chr9:128556300
|
AC | A | 3 | a0001c0001t0001g0156a0001c0002t0001g0268a0001c0002t0001g0269 | 3 | NA18957.hp2 NA18982.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-4+3605delC | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556300 | ||||||
| chr9:128556301
|
C | A | 291 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.-4+3605C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556301 | ||||||
| chr9:128556341
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-4+3645A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556341 | ||||||
| chr9:128556570
|
A | T | 1 | a0001c0001t0001g0155 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-4+3874A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556570 | ||||||
| chr9:128556894
|
A | G | 4 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | NA18969.hp1 NA18974.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4+4198A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556894 | ||||||
| chr9:128556923
|
G | A | 4 | a0001c0001t0001g0303a0001c0010t0001g0300a0001c0010t0001g0301others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+4227G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128556923 | ||||||
| chr9:128557133
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-4+4437A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557133 | ||||||
| chr9:128557268
|
G | A | 294 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-4+4572G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557268 | ||||||
| chr9:128557318
|
A | G | 9 | a0002c0004t0001g0285a0002c0004t0002g0277a0002c0004t0002g0278others(6): Show | 9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4+4622A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557318 | ||||||
| chr9:128557366
|
A | G | 9 | a0002c0004t0001g0285a0002c0004t0002g0277a0002c0004t0002g0278others(6): Show | 9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4+4670A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557366 | ||||||
| chr9:128557588
|
C | CCCCCAAA others(23): Show |
1 | a0001c0001t0001g0166 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-4+4901_-4+4930dup others(30): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128557588 | |||||
| chr9:128557660
|
G | A | 294 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-4+4964G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557660 | ||||||
| chr9:128557711
|
A | G | 3 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0267 | 3 | HG01884.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-4+5015A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557711 | ||||||
| chr9:128557798
|
TC | T | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-4+5103delC | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557798 | ||||||
| chr9:128557799
|
C | CT | 8 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0178others(5): Show | 8 | HG02109.hp1 HG03669.hp2 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4+5125dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128557799 | |||||
| chr9:128557799
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-4+5103C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557799 | ||||||
| chr9:128557799
|
CT | C | 87 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(84): Show | 87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-4+5125delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128557799 | |||||
| chr9:128557799
|
CTT | C | 140 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-4+5124_-4+5125del others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128557799 | |||||
| chr9:128557961
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-4+5265G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128557961 | ||||||
| chr9:128558005
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-4+5309G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558005 | ||||||
| chr9:128558093
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-4+5397G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558093 | ||||||
| chr9:128558094
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-4+5398C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558094 | ||||||
| chr9:128558100
|
G | A | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-4+5404G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558100 | ||||||
| chr9:128558174
|
T | C | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-4+5478T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558174 | ||||||
| chr9:128558260
|
C | G | 122 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(119): Show | 122 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.-4+5564C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558260 | ||||||
| chr9:128558326
|
C | T | 1 | a0001c0016t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-4+5630C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558326 | ||||||
| chr9:128558530
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-4+5834G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558530 | ||||||
| chr9:128558632
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0139 | 3 | HG02145.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-4+5936T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558632 | ||||||
| chr9:128558639
|
T | C | 114 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(111): Show | 114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-4+5943T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558639 | ||||||
| chr9:128558761
|
C | T | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-4+6065C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558761 | ||||||
| chr9:128558792
|
C | T | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-4+6096C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558792 | ||||||
| chr9:128558888
|
C | T | 1 | a0001c0002t0001g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-4+6192C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558888 | ||||||
| chr9:128558933
|
A | C | 1 | a0001c0005t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-4+6237A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558933 | ||||||
| chr9:128558997
|
T | C | 29 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0055others(26): Show | 29 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.-4+6301T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128558997 | ||||||
| chr9:128559022
|
G | A | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-4+6326G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559022 | ||||||
| chr9:128559141
|
C | A | 1 | a0001c0002t0001g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-4+6445C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559141 | ||||||
| chr9:128559221
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-4+6525G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559221 | ||||||
| chr9:128559500
|
G | A | 2 | a0001c0001t0001g0071a0001c0002t0005g0227 | 2 | HG01433.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-4+6804G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559500 | ||||||
| chr9:128559626
|
C | T | 1 | a0001c0002t0001g0225 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-4+6930C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559626 | ||||||
| chr9:128559735
|
A | AT | 22 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0064others(19): Show | 22 | HG00140.hp2 HG00621.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-3-6989dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128559735 | |||||
| chr9:128559798
|
G | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0034a0001c0001t0001g0035others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.-3-6940G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559798 | ||||||
| chr9:128559838
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-3-6900G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559838 | ||||||
| chr9:128559884
|
G | A | 1 | a0001c0025t0001g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3-6854G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128559884 | ||||||
| chr9:128560029
|
C | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0133 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-3-6709C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560029 | ||||||
| chr9:128560084
|
C | CTT | 15 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0003t0001g0086others(12): Show | 15 | HG02040.hp2 HG02615.hp2 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3-6640_-3-6639dup others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128560084 | |||||
| chr9:128560084
|
C | CTTT | 165 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.-3-6641_-3-6639dup others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128560084 | |||||
| chr9:128560084
|
C | CTTTT | 103 | a0001c0001t0001g0043a0001c0001t0001g0166a0001c0001t0001g0286others(100): Show | 103 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-3-6642_-3-6639dup others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128560084 | |||||
| chr9:128560084
|
C | CTTTTT | 12 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(9): Show | 12 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-6643_-3-6639dup others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128560084 | |||||
| chr9:128560107
|
A | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0141 | 2 | NA18947.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-3-6631A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560107 | ||||||
| chr9:128560145
|
G | A | 5 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0183others(2): Show | 5 | HG00642.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-6593G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560145 | ||||||
| chr9:128560169
|
A | G | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-3-6569A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560169 | ||||||
| chr9:128560228
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-3-6510C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560228 | ||||||
| chr9:128560233
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-3-6505G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560233 | ||||||
| chr9:128560368
|
G | A | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-3-6370G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560368 | ||||||
| chr9:128560373
|
C | T | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-6365C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560373 | ||||||
| chr9:128560382
|
C | CT | 16 | a0001c0001t0001g0063a0001c0001t0001g0084a0001c0001t0001g0132others(13): Show | 16 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.-3-6340dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128560382 | |||||
| chr9:128560466
|
C | T | 1 | a0001c0002t0005g0227 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-3-6272C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560466 | ||||||
| chr9:128560474
|
A | G | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-3-6264A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560474 | ||||||
| chr9:128560495
|
C | T | 113 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(110): Show | 113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.-3-6243C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560495 | ||||||
| chr9:128560632
|
C | CG | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-3-6105dupG | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128560632 | |||||
| chr9:128560675
|
T | A | 1 | a0001c0002t0001g0184 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-3-6063T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560675 | ||||||
| chr9:128560999
|
G | C | 113 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(110): Show | 113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.-3-5739G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128560999 | ||||||
| chr9:128561015
|
C | CA | 114 | a0001c0001t0001g0072a0001c0001t0001g0288a0001c0002t0001g0001others(111): Show | 114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-3-5703dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561015 | |||||
| chr9:128561015
|
C | CAA | 142 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(139): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-3-5704_-3-5703dup others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561015 | |||||
| chr9:128561015
|
CA | C | 7 | a0001c0001t0001g0303a0001c0005t0001g0015a0001c0005t0001g0016others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-5703delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561015 | |||||
| chr9:128561033
|
A | AAG | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-5704_-3-5703ins others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561033 | |||||
| chr9:128561096
|
A | G | 9 | a0002c0004t0001g0285a0002c0004t0002g0277a0002c0004t0002g0278others(6): Show | 9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-5642A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561096 | ||||||
| chr9:128561110
|
C | T | 1 | a0001c0003t0001g0149 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-3-5628C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561110 | ||||||
| chr9:128561144
|
C | T | 9 | a0002c0004t0001g0285a0002c0004t0002g0277a0002c0004t0002g0278others(6): Show | 9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-5594C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561144 | ||||||
| chr9:128561145
|
G | A | 1 | a0001c0014t0003g0019 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-3-5593G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561145 | ||||||
| chr9:128561278
|
C | G | 2 | a0001c0001t0001g0037a0001c0001t0001g0138 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-3-5460C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561278 | ||||||
| chr9:128561278
|
C | T | 1 | a0002c0004t0002g0276 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-3-5460C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561278 | ||||||
| chr9:128561313
|
A | G | 4 | a0001c0001t0001g0303a0001c0010t0001g0300a0001c0010t0001g0301others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-5425A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561313 | ||||||
| chr9:128561391
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0158 | 2 | NA18941.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-3-5347C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561391 | ||||||
| chr9:128561430
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-3-5308G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561430 | ||||||
| chr9:128561466
|
A | G | 1 | a0001c0002t0001g0305 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-3-5272A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561466 | ||||||
| chr9:128561587
|
G | T | 288 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-3-5151G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561587 | ||||||
| chr9:128561611
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-3-5127C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561611 | ||||||
| chr9:128561620
|
A | G | 302 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.-3-5118A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561620 | ||||||
| chr9:128561662
|
C | CA | 18 | a0001c0001t0001g0082a0001c0001t0001g0126a0001c0001t0001g0288others(15): Show | 18 | HG00280.hp1 HG01515.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.-3-5050dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAA | 8 | a0001c0001t0001g0125a0001c0001t0001g0138a0001c0007t0001g0273others(5): Show | 8 | HG02572.hp2 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-5051_-3-5050dup others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAA | 8 | a0001c0001t0001g0036a0001c0001t0001g0081a0001c0001t0001g0155others(5): Show | 8 | HG01934.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-5052_-3-5050dup others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAA | 63 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0174others(60): Show | 63 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-3-5053_-3-5050dup others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAA | 32 | a0001c0002t0001g0003a0001c0002t0001g0178a0001c0002t0001g0180others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-3-5054_-3-5050dup others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAA | 12 | a0001c0001t0001g0147a0001c0002t0001g0188a0001c0002t0001g0221others(9): Show | 12 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3-5055_-3-5050dup others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA | 7 | a0001c0001t0001g0158a0001c0002t0001g0219a0001c0002t0001g0220others(4): Show | 7 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-5056_-3-5050dup others(7): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-3-5060_-3-5050dup others(11): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0044a0001c0001t0001g0133a0001c0003t0001g0124others(1): Show | 4 | HG02083.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-5061_-3-5050dup others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(6): Show |
21 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0035others(18): Show | 21 | HG00140.hp1 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-3-5062_-3-5050dup others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(7): Show |
35 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0034others(32): Show | 35 | HG00408.hp2 HG00621.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-3-5063_-3-5050dup others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(8): Show |
24 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0052others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.-3-5064_-3-5050dup others(15): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(9): Show |
8 | a0001c0001t0001g0051a0001c0001t0001g0074a0001c0001t0001g0105others(5): Show | 8 | HG01123.hp2 HG02738.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-5065_-3-5050dup others(16): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(10): Show |
6 | a0001c0001t0001g0073a0001c0001t0001g0104a0001c0001t0001g0136others(3): Show | 6 | HG01496.hp1 HG01891.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-5066_-3-5050dup others(17): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(11): Show |
4 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0142others(1): Show | 4 | HG02135.hp1 HG03654.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-5067_-3-5050dup others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(12): Show |
6 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0099others(3): Show | 6 | HG02809.hp2 HG02818.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-5068_-3-5050dup others(19): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(13): Show |
9 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG01981.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-5069_-3-5050dup others(20): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(14): Show |
2 | a0001c0001t0001g0064a0001c0001t0001g0130 | 2 | NA18955.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-3-5070_-3-5050dup others(21): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(15): Show |
5 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG00558.hp1 HG00597.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-5071_-3-5050dup others(22): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-3-5072_-3-5050dup others(23): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-3-5074_-3-5050dup others(25): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0088 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-3-5050_-3-5049ins others(31): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561662
|
CAA | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0128a0001c0001t0001g0304others(3): Show | 6 | HG02071.hp2 HG02559.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-5051_-3-5050del others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128561662 | |||||
| chr9:128561686
|
A | G | 1 | a0001c0007t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-3-5052A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561686 | ||||||
| chr9:128561689
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-3-5049G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561689 | ||||||
| chr9:128561789
|
A | G | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-3-4949A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561789 | ||||||
| chr9:128561961
|
T | C | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-4777T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561961 | ||||||
| chr9:128561995
|
C | T | 9 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0062others(6): Show | 9 | HG00408.hp2 NA18941.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3-4743C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128561995 | ||||||
| chr9:128562028
|
A | G | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-3-4710A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562028 | ||||||
| chr9:128562132
|
T | A | 150 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-3-4606T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562132 | ||||||
| chr9:128562163
|
C | T | 12 | a0001c0001t0001g0303a0001c0006t0001g0292a0001c0006t0001g0293others(9): Show | 12 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-4575C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562163 | ||||||
| chr9:128562215
|
G | C | 1 | a0001c0002t0001g0305 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-3-4523G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562215 | ||||||
| chr9:128562283
|
A | G | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-4455A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562283 | ||||||
| chr9:128562541
|
C | T | 173 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-3-4197C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562541 | ||||||
| chr9:128562708
|
A | ATAT | 294 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-3-4027_-3-4025dup others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562708 | |||||
| chr9:128562774
|
C | T | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-3-3964C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562774 | ||||||
| chr9:128562780
|
C | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0165 | 2 | NA19012.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-3-3958C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562780 | ||||||
| chr9:128562788
|
C | A | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-3-3950C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562788 | ||||||
| chr9:128562789
|
G | C | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-3949G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562789 | ||||||
| chr9:128562822
|
G | T | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-3-3916G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562822 | ||||||
| chr9:128562887
|
C | T | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-3-3851C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562887 | ||||||
| chr9:128562943
|
C | T | 12 | a0001c0001t0001g0303a0001c0006t0001g0292a0001c0006t0001g0293others(9): Show | 12 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-3795C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562943 | ||||||
| chr9:128562969
|
AAAATATA others(17): Show |
A | 20 | a0001c0002t0001g0180a0001c0002t0001g0219a0001c0002t0001g0220others(17): Show | 20 | HG02040.hp2 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-3-3767_-3-3744del others(24): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562969 | |||||
| chr9:128562969
|
AAAATATA others(19): Show |
A | 114 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(111): Show | 114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-3-3767_-3-3742del others(26): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562969 | |||||
| chr9:128562970
|
AAATATAT others(15): Show |
A | 5 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0003t0001g0123others(2): Show | 5 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-3767_-3-3746del others(22): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562970 | ||||||
| chr9:128562971
|
A | T | 139 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.-3-3767A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562971 | ||||||
| chr9:128562971
|
AATATATA others(12): Show |
A | 1 | a0001c0001t0001g0158 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-3-3766_-3-3748del others(19): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562971 | ||||||
| chr9:128562974
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-3-3755_-3-3738del others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562974 | |||||
| chr9:128562983
|
CATGTATG others(3): Show |
C | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-3-3752_-3-3743del others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | |||||
| chr9:128562983
|
CATGTATG others(5): Show |
C | 1 | a0001c0001t0001g0041 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-3-3752_-3-3741del others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | |||||
| chr9:128562983
|
CATGTATG others(7): Show |
C | 14 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0088others(11): Show | 14 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.-3-3752_-3-3739del others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | |||||
| chr9:128562983
|
CATGTATG others(9): Show |
C | 17 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0051others(14): Show | 17 | HG00140.hp2 HG00642.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-3-3752_-3-3737del others(16): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | |||||
| chr9:128562983
|
CATGTATG others(11): Show |
C | 71 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.-3-3752_-3-3735del others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | |||||
| chr9:128562983
|
CATGTATG others(13): Show |
C | 32 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0044others(29): Show | 32 | HG00735.hp2 HG01257.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.-3-3752_-3-3733del others(20): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | |||||
| chr9:128562983
|
CATGTATG others(15): Show |
C | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-3752_-3-3731del others(22): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | |||||
| chr9:128562983
|
CATGTATG others(19): Show |
C | 12 | a0001c0001t0001g0303a0001c0006t0001g0292a0001c0006t0001g0293others(9): Show | 12 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-3752_-3-3727del others(26): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562983 | |||||
| chr9:128562990
|
G | GTATATAT others(3): Show |
1 | a0001c0014t0003g0019 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-3-3747_-3-3746ins others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562990 | |||||
| chr9:128562990
|
G | GTATATAT others(9): Show |
1 | a0001c0014t0003g0018 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-3-3747_-3-3746ins others(16): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562990 | |||||
| chr9:128562990
|
GTGTATAT others(3): Show |
G | 1 | a0001c0016t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-3-3746_-3-3737del others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562990 | |||||
| chr9:128562992
|
G | A | 6 | a0001c0001t0001g0158a0001c0009t0001g0004a0001c0009t0001g0025others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-3746G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128562992 | ||||||
| chr9:128562992
|
G | GTATGTAT others(11): Show |
3 | a0001c0005t0001g0013a0001c0005t0001g0014a0001c0005t0001g0016 | 3 | HG02723.hp1 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-3-3743_-3-3742ins others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562992 | |||||
| chr9:128562992
|
G | GTATGTAT others(13): Show |
1 | a0001c0005t0001g0015 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-3-3743_-3-3742ins others(20): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562992 | |||||
| chr9:128562992
|
G | GTATGTAT others(17): Show |
1 | a0001c0005t0001g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-3-3743_-3-3742ins others(24): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128562992 | |||||
| chr9:128563002
|
A | G | 1 | a0001c0017t0006g0012 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-3-3736A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563002 | ||||||
| chr9:128563003
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-3-3735T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563003 | ||||||
| chr9:128563004
|
A | G | 1 | a0001c0002t0001g0269 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-3-3734A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563004 | ||||||
| chr9:128563005
|
T | C | 5 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0003t0001g0123others(2): Show | 5 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-3733T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563005 | ||||||
| chr9:128563007
|
T | C | 20 | a0001c0002t0001g0180a0001c0002t0001g0219a0001c0002t0001g0220others(17): Show | 20 | HG02040.hp2 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-3-3731T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563007 | ||||||
| chr9:128563009
|
T | C | 114 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(111): Show | 114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-3-3729T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563009 | ||||||
| chr9:128563024
|
A | G | 5 | a0001c0005t0001g0013a0001c0005t0001g0014a0001c0005t0001g0015others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-3714A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563024 | ||||||
| chr9:128563028
|
G | A | 1 | a0001c0016t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-3-3710G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563028 | ||||||
| chr9:128563239
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3499A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563239 | ||||||
| chr9:128563240
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3498A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563240 | ||||||
| chr9:128563241
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3497C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563241 | ||||||
| chr9:128563244
|
C | G | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3494C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563244 | ||||||
| chr9:128563245
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3493A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563245 | ||||||
| chr9:128563247
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3491C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563247 | ||||||
| chr9:128563249
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3489G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563249 | ||||||
| chr9:128563251
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3487A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563251 | ||||||
| chr9:128563254
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3484A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563254 | ||||||
| chr9:128563256
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3482A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563256 | ||||||
| chr9:128563257
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3481A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563257 | ||||||
| chr9:128563258
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3480A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563258 | ||||||
| chr9:128563260
|
A | G | 5 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-3478A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563260 | ||||||
| chr9:128563262
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3476A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563262 | ||||||
| chr9:128563264
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3474A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563264 | ||||||
| chr9:128563265
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3473A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563265 | ||||||
| chr9:128563271
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3467C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563271 | ||||||
| chr9:128563275
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3463G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563275 | ||||||
| chr9:128563277
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3461G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563277 | ||||||
| chr9:128563279
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3459G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563279 | ||||||
| chr9:128563280
|
C | A | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3458C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563280 | ||||||
| chr9:128563282
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3456G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563282 | ||||||
| chr9:128563289
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3449G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563289 | ||||||
| chr9:128563291
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3447C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563291 | ||||||
| chr9:128563293
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3445G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563293 | ||||||
| chr9:128563301
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3-3437A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563301 | ||||||
| chr9:128563321
|
C | T | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-3-3417C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563321 | ||||||
| chr9:128563426
|
C | A | 1 | a0001c0002t0001g0228 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-3-3312C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563426 | ||||||
| chr9:128563524
|
T | C | 4 | a0001c0001t0001g0303a0001c0010t0001g0300a0001c0010t0001g0301others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-3214T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563524 | ||||||
| chr9:128563587
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-3-3151C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563587 | ||||||
| chr9:128563673
|
C | T | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-3065C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563673 | ||||||
| chr9:128563715
|
C | CT | 13 | a0001c0002t0001g0199a0001c0002t0001g0261a0001c0005t0001g0023others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-3-3005dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128563715 | |||||
| chr9:128563715
|
CT | C | 22 | a0001c0001t0001g0055a0001c0001t0001g0133a0001c0001t0001g0303others(19): Show | 22 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.-3-3005delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128563715 | |||||
| chr9:128563782
|
T | C | 1 | a0001c0002t0001g0200 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-3-2956T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563782 | ||||||
| chr9:128563957
|
G | A | 302 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.-3-2781G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563957 | ||||||
| chr9:128563994
|
C | T | 14 | a0001c0001t0001g0303a0001c0002t0001g0030a0001c0002t0001g0031others(11): Show | 14 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3-2744C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128563994 | ||||||
| chr9:128564159
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-3-2579G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564159 | ||||||
| chr9:128564163
|
G | T | 114 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(111): Show | 114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.-3-2575G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564163 | ||||||
| chr9:128564173
|
C | T | 9 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0007t0001g0007others(6): Show | 9 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3-2565C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564173 | ||||||
| chr9:128564247
|
C | T | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-3-2491C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564247 | ||||||
| chr9:128564351
|
A | G | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-3-2387A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564351 | ||||||
| chr9:128564420
|
GA | G | 9 | a0002c0004t0001g0285a0002c0004t0002g0277a0002c0004t0002g0278others(6): Show | 9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-2304delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128564420 | |||||
| chr9:128564436
|
T | C | 264 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-3-2302T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564436 | ||||||
| chr9:128564516
|
G | A | 14 | a0001c0001t0001g0303a0001c0002t0001g0030a0001c0002t0001g0031others(11): Show | 14 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3-2222G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564516 | ||||||
| chr9:128564572
|
C | T | 3 | a0001c0009t0001g0004a0001c0009t0001g0025a0001c0009t0001g0026 | 3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-3-2166C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564572 | ||||||
| chr9:128564580
|
C | CAAAT | 295 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-3-2142_-3-2139dup others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | INFO_REALIGN_3_PRIME | chr9 | 128564580 | |||||
| chr9:128564930
|
G | A | 4 | a0001c0002t0001g0230a0001c0002t0001g0236a0001c0002t0001g0237others(1): Show | 4 | NA18968.hp2 NA18982.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-1808G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564930 | ||||||
| chr9:128564940
|
T | G | 4 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0007t0001g0045others(1): Show | 4 | HG02922.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-1798T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564940 | ||||||
| chr9:128564968
|
T | C | 1 | a0002c0004t0002g0279 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-3-1770T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128564968 | ||||||
| chr9:128565189
|
G | A | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-3-1549G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565189 | ||||||
| chr9:128565286
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-3-1452C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565286 | ||||||
| chr9:128565322
|
A | G | 3 | a0001c0001t0001g0038a0001c0014t0003g0018a0001c0014t0003g0019 | 3 | HG02559.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-3-1416A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565322 | ||||||
| chr9:128565455
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-3-1283T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565455 | ||||||
| chr9:128565703
|
C | A | 112 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(109): Show | 112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3-1035C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565703 | ||||||
| chr9:128565764
|
A | G | 295 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-3-974A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565764 | ||||||
| chr9:128565810
|
C | T | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-3-928C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128565810 | ||||||
| chr9:128566118
|
G | A | 3 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0267 | 3 | HG01884.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-3-620G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128566118 | ||||||
| chr9:128566243
|
A | C | 295 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-3-495A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128566243 | ||||||
| chr9:128566346
|
G | A | 1 | a0001c0025t0001g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3-392G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128566346 | ||||||
| chr9:128566561
|
C | T | 9 | a0002c0004t0001g0285a0002c0004t0002g0277a0002c0004t0002g0278others(6): Show | 9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-177C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128566561 | ||||||
| chr9:128566657
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-3-81T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 1/56 | chr9 | 128566657 | ||||||
| chr9:128567123
|
C | T | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.237+146C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567123 | ||||||
| chr9:128567193
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0139 | 3 | HG02145.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.237+216G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567193 | ||||||
| chr9:128567312
|
G | A | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.237+335G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567312 | ||||||
| chr9:128567401
|
C | T | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.237+424C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567401 | ||||||
| chr9:128567411
|
C | A | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.237+434C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567411 | ||||||
| chr9:128567432
|
C | T | 1 | a0001c0026t0001g0198 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.237+455C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567432 | ||||||
| chr9:128567804
|
A | G | 151 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.237+827A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128567804 | ||||||
| chr9:128568065
|
ACT | A | 5 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-706_238-705del others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568065 | ||||||
| chr9:128568068
|
T | A | 5 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-704T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568068 | ||||||
| chr9:128568074
|
A | G | 7 | a0001c0003t0001g0028a0001c0003t0001g0086a0001c0003t0001g0108others(4): Show | 7 | HG01109.hp2 NA18948.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.238-698A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568074 | ||||||
| chr9:128568202
|
C | G | 1 | a0001c0026t0001g0198 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.238-570C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568202 | ||||||
| chr9:128568240
|
C | G | 153 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.238-532C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568240 | ||||||
| chr9:128568286
|
G | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-486G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568286 | ||||||
| chr9:128568355
|
G | A | 111 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(108): Show | 111 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.238-417G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568355 | ||||||
| chr9:128568407
|
A | C | 9 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0007t0001g0007others(6): Show | 9 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.238-365A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568407 | ||||||
| chr9:128568420
|
G | C | 9 | a0002c0004t0001g0285a0002c0004t0002g0277a0002c0004t0002g0278others(6): Show | 9 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.238-352G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568420 | ||||||
| chr9:128568706
|
A | G | 8 | a0002c0004t0001g0285a0002c0004t0002g0277a0002c0004t0002g0278others(5): Show | 8 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-66A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568706 | ||||||
| chr9:128568710
|
C | G | 8 | a0002c0004t0001g0285a0002c0004t0002g0277a0002c0004t0002g0278others(5): Show | 8 | HG02040.hp2 NA18949.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-62C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 2/56 | chr9 | 128568710 | ||||||
| chr9:128569041
|
C | T | 145 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.363+144C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569041 | ||||||
| chr9:128569087
|
T | C | 3 | a0001c0003t0001g0123a0001c0003t0001g0127a0001c0027t0001g0113 | 3 | HG00408.hp1 HG00609.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.363+190T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569087 | ||||||
| chr9:128569171
|
A | G | 112 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(109): Show | 112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.363+274A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569171 | ||||||
| chr9:128569327
|
C | CTGAG | 13 | a0001c0002t0001g0010a0001c0002t0001g0011a0002c0004t0001g0285others(10): Show | 13 | HG02040.hp2 HG03225.hp1 HG03669.hp2 others(10): Show |
intron_variant | MODIFIER | c.363+430_363+431ins others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569327 | ||||||
| chr9:128569580
|
T | A | 1 | a0001c0002t0001g0201 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.363+683T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569580 | ||||||
| chr9:128569745
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.363+848C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569745 | ||||||
| chr9:128569768
|
A | C | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.363+871A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569768 | ||||||
| chr9:128569986
|
T | C | 1 | a0001c0025t0001g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.363+1089T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128569986 | ||||||
| chr9:128570064
|
A | T | 1 | a0001c0001t0001g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.363+1167A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570064 | ||||||
| chr9:128570269
|
A | C | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+1372A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570269 | ||||||
| chr9:128570282
|
C | A | 112 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(109): Show | 112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.363+1385C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570282 | ||||||
| chr9:128570304
|
T | TTATA | 3 | a0001c0002t0001g0010a0001c0005t0001g0014a0001c0017t0006g0012 | 3 | HG01109.hp2 HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+1431_363+1434d others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570304 | |||||
| chr9:128570322
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0156 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.363+1427_363+1443d others(19): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570322 | |||||
| chr9:128570324
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0100 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.363+1429_363+1439d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570324 | |||||
| chr9:128570326
|
ATATATTT others(2): Show |
A | 19 | a0001c0002t0001g0181a0001c0002t0001g0196a0001c0002t0001g0197others(16): Show | 19 | HG01123.hp1 HG01934.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.363+1431_363+1439d others(11): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570326 | |||||
| chr9:128570326
|
ATATATTT others(3): Show |
A | 2 | a0001c0002t0001g0211a0001c0002t0001g0220 | 2 | HG01257.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.363+1431_363+1440d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570326 | |||||
| chr9:128570326
|
ATATATTT others(4): Show |
A | 12 | a0001c0001t0001g0040a0001c0001t0001g0046a0001c0001t0001g0048others(9): Show | 12 | HG01167.hp1 HG01256.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.363+1431_363+1441d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570326 | |||||
| chr9:128570326
|
ATATATTT others(5): Show |
A | 3 | a0001c0001t0001g0034a0001c0001t0001g0114a0001c0001t0001g0165 | 3 | HG01515.hp1 NA18964.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.363+1431_363+1442d others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570326 | |||||
| chr9:128570328
|
ATATTTTT others(2): Show |
A | 51 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0031others(48): Show | 51 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.363+1433_363+1441d others(11): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570328 | |||||
| chr9:128570328
|
ATATTTTT others(3): Show |
A | 29 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0094others(26): Show | 29 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.363+1433_363+1442d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570328 | |||||
| chr9:128570328
|
ATATTTTT others(4): Show |
A | 53 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0041others(50): Show | 53 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.363+1433_363+1443d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570328 | |||||
| chr9:128570328
|
ATATTTTT others(5): Show |
A | 4 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0148others(1): Show | 4 | NA18954.hp2 NA18979.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1433_363+1444d others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570328 | |||||
| chr9:128570330
|
A | ATATATAT others(15): Show |
1 | a0002c0004t0002g0280 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.363+1434_363+1435i others(24): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
A | ATATATAT others(17): Show |
1 | a0002c0004t0002g0279 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.363+1434_363+1435i others(26): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
A | ATATATAT others(14): Show |
1 | a0002c0004t0002g0277 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.363+1434_363+1435i others(23): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
A | ATATATAT others(17): Show |
1 | a0002c0004t0002g0284 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.363+1434_363+1435i others(26): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
A | ATATATAT others(10): Show |
1 | a0002c0004t0002g0281 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.363+1434_363+1435i others(19): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
A | ATATATAT others(15): Show |
1 | a0002c0004t0001g0285 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.363+1434_363+1435i others(24): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
A | ATATATAT others(9): Show |
1 | a0002c0004t0002g0278 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.363+1434_363+1435i others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
A | ATATATAT others(9): Show |
1 | a0002c0004t0002g0282 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.363+1434_363+1435i others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
A | ATATATAT others(13): Show |
1 | a0002c0004t0002g0275 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.363+1434_363+1435i others(22): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
A | ATATATAT others(10): Show |
1 | a0002c0004t0002g0276 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.363+1434_363+1435i others(19): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
A | ATTTTTTT others(4): Show |
1 | a0002c0004t0002g0283 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.363+1447_363+1457d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
A | T | 3 | a0001c0005t0001g0020a0001c0005t0001g0022a0001c0014t0003g0018 | 3 | HG02486.hp1 HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.363+1433A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570330 | ||||||
| chr9:128570330
|
ATTTTTTT | A | 20 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(17): Show | 20 | HG00099.hp1 HG00597.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.363+1451_363+1457d others(9): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
ATTTTTTT others(1): Show |
A | 6 | a0001c0002t0001g0183a0001c0002t0001g0225a0001c0002t0001g0241others(3): Show | 6 | HG00642.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+1450_363+1457d others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
ATTTTTTT others(2): Show |
A | 26 | a0001c0001t0001g0027a0001c0001t0001g0056a0001c0001t0001g0068others(23): Show | 26 | HG00558.hp2 HG00735.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.363+1449_363+1457d others(11): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0092others(4): Show | 7 | HG02258.hp2 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+1448_363+1457d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570330
|
ATTTTTTT others(4): Show |
A | 26 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(23): Show | 26 | HG00140.hp1 HG00280.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.363+1447_363+1457d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570330 | |||||
| chr9:128570331
|
T | TA | 3 | a0001c0005t0001g0013a0001c0005t0001g0015a0001c0005t0001g0016 | 3 | HG02055.hp2 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.363+1434_363+1435i others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570331 | ||||||
| chr9:128570332
|
T | A | 4 | a0001c0002t0001g0010a0001c0005t0001g0014a0001c0005t0001g0023others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1435T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570332 | ||||||
| chr9:128570334
|
T | A | 2 | a0001c0005t0001g0023a0001c0007t0001g0273 | 2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.363+1437T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570334 | ||||||
| chr9:128570336
|
T | A | 2 | a0001c0007t0001g0045a0001c0007t0001g0273 | 2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.363+1439T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570336 | ||||||
| chr9:128570337
|
T | A | 2 | a0001c0002t0001g0174a0001c0002t0001g0204 | 2 | NA18952.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.363+1440T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570337 | ||||||
| chr9:128570338
|
T | A | 4 | a0001c0002t0001g0184a0001c0002t0001g0190a0001c0007t0001g0273others(1): Show | 4 | HG02615.hp2 HG02717.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1441T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570338 | ||||||
| chr9:128570339
|
T | A | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(10): Show | 13 | HG00099.hp1 HG00597.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.363+1442T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570339 | ||||||
| chr9:128570340
|
T | A | 3 | a0001c0002t0001g0225a0001c0007t0001g0273a0001c0007t0001g0274 | 3 | HG01361.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.363+1443T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570340 | ||||||
| chr9:128570341
|
T | A | 11 | a0001c0001t0001g0056a0001c0001t0001g0065a0001c0001t0001g0067others(8): Show | 11 | HG01433.hp2 HG02683.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.363+1444T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570341 | ||||||
| chr9:128570342
|
T | A | 3 | a0001c0001t0007g0061a0001c0007t0001g0273a0001c0007t0001g0274 | 3 | HG02615.hp2 HG02717.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.363+1445T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570342 | ||||||
| chr9:128570343
|
T | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0078a0001c0001t0001g0154 | 3 | NA18953.hp1 NA19057.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.363+1446T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570343 | ||||||
| chr9:128570348
|
T | G | 1 | a0001c0002t0001g0207 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.363+1451T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570348 | ||||||
| chr9:128570432
|
G | A | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.363+1535G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570432 | ||||||
| chr9:128570499
|
G | A | 112 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(109): Show | 112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.363+1602G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570499 | ||||||
| chr9:128570645
|
C | CTTAT | 5 | a0001c0002t0001g0030a0001c0002t0001g0031a0003c0011t0001g0057others(2): Show | 5 | NA18980.hp1 NA18998.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1771_363+1774d others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128570645 | |||||
| chr9:128570725
|
C | T | 112 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(109): Show | 112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.363+1828C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570725 | ||||||
| chr9:128570989
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.363+2092A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128570989 | ||||||
| chr9:128571003
|
C | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+2106C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571003 | ||||||
| chr9:128571044
|
G | A | 11 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(8): Show | 11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.363+2147G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571044 | ||||||
| chr9:128571090
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.363+2193C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571090 | ||||||
| chr9:128571140
|
A | G | 1 | a0001c0007t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.363+2243A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571140 | ||||||
| chr9:128571156
|
G | T | 1 | a0001c0002t0001g0201 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.363+2259G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571156 | ||||||
| chr9:128571165
|
C | A | 1 | a0001c0007t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.363+2268C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571165 | ||||||
| chr9:128571291
|
G | GA | 149 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.363+2405dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128571291 | |||||
| chr9:128571484
|
C | T | 1 | a0001c0007t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.363+2587C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571484 | ||||||
| chr9:128571719
|
A | G | 7 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+2822A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571719 | ||||||
| chr9:128571844
|
A | G | 7 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-2831A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128571844 | ||||||
| chr9:128572086
|
C | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-2589C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572086 | ||||||
| chr9:128572329
|
GA | G | 113 | a0001c0001t0001g0158a0001c0002t0001g0001a0001c0002t0001g0002others(110): Show | 113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.364-2344delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128572329 | |||||
| chr9:128572460
|
C | A | 1 | a0001c0001t0001g0064 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.364-2215C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572460 | ||||||
| chr9:128572465
|
C | T | 123 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(120): Show | 123 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.364-2210C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572465 | ||||||
| chr9:128572477
|
C | CT | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.364-2195dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128572477 | |||||
| chr9:128572488
|
G | A | 145 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.364-2187G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572488 | ||||||
| chr9:128572563
|
T | G | 283 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.364-2112T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572563 | ||||||
| chr9:128572611
|
A | G | 283 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.364-2064A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572611 | ||||||
| chr9:128572834
|
G | GT | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.364-1840dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | INFO_REALIGN_3_PRIME | chr9 | 128572834 | |||||
| chr9:128572977
|
C | T | 3 | a0001c0009t0001g0004a0001c0009t0001g0025a0001c0009t0001g0026 | 3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.364-1698C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128572977 | ||||||
| chr9:128573062
|
A | G | 283 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.364-1613A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573062 | ||||||
| chr9:128573385
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.364-1290A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573385 | ||||||
| chr9:128573394
|
A | G | 151 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.364-1281A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573394 | ||||||
| chr9:128573473
|
C | T | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.364-1202C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573473 | ||||||
| chr9:128573648
|
G | A | 37 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0038others(34): Show | 37 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.364-1027G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573648 | ||||||
| chr9:128573676
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.364-999G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573676 | ||||||
| chr9:128573719
|
G | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-956G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573719 | ||||||
| chr9:128573745
|
C | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-930C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573745 | ||||||
| chr9:128573784
|
C | T | 11 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(8): Show | 11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-891C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573784 | ||||||
| chr9:128573815
|
A | C | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.364-860A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573815 | ||||||
| chr9:128573841
|
A | C | 283 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.364-834A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573841 | ||||||
| chr9:128573846
|
C | G | 153 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.364-829C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573846 | ||||||
| chr9:128573955
|
A | G | 283 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.364-720A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573955 | ||||||
| chr9:128573988
|
C | T | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-687C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128573988 | ||||||
| chr9:128574023
|
A | G | 283 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.364-652A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574023 | ||||||
| chr9:128574028
|
C | G | 11 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(8): Show | 11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-647C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574028 | ||||||
| chr9:128574043
|
G | A | 112 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(109): Show | 112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.364-632G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574043 | ||||||
| chr9:128574320
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA18972.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.364-355T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574320 | ||||||
| chr9:128574371
|
G | T | 143 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.364-304G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574371 | ||||||
| chr9:128574480
|
A | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-195A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574480 | ||||||
| chr9:128574578
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0067 | 2 | NA18939.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.364-97G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574578 | ||||||
| chr9:128574578
|
G | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-97G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574578 | ||||||
| chr9:128574588
|
G | T | 1 | a0001c0010t0001g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.364-87G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 3/56 | chr9 | 128574588 | ||||||
| chr9:128574972
|
G | GCTCTCCA others(16): Show |
2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.504+157_504+158ins others(23): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128574972 | ||||||
| chr9:128574974
|
A | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.504+159A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128574974 | ||||||
| chr9:128574976
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.504+161G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128574976 | ||||||
| chr9:128574977
|
T | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.504+162T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128574977 | ||||||
| chr9:128575023
|
C | T | 285 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.505-176C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128575023 | ||||||
| chr9:128575110
|
C | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.505-89C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128575110 | ||||||
| chr9:128575111
|
G | A | 1 | a0001c0005t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.505-88G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 4/56 | chr9 | 128575111 | ||||||
| chr9:128575382
|
A | C | 283 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.651+37A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575382 | ||||||
| chr9:128575398
|
A | G | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.651+53A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575398 | ||||||
| chr9:128575458
|
G | A | 9 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0007t0001g0007others(6): Show | 9 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+113G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575458 | ||||||
| chr9:128575480
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.651+135T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575480 | ||||||
| chr9:128575564
|
A | G | 151 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.651+219A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575564 | ||||||
| chr9:128575592
|
G | C | 1 | a0001c0002t0001g0270 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.651+247G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575592 | ||||||
| chr9:128575667
|
G | A | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.651+322G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575667 | ||||||
| chr9:128575680
|
G | A | 1 | a0001c0002t0001g0192 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.651+335G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128575680 | ||||||
| chr9:128576179
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.652-644A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128576179 | ||||||
| chr9:128576321
|
A | G | 285 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.652-502A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128576321 | ||||||
| chr9:128576425
|
C | T | 7 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-398C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128576425 | ||||||
| chr9:128576450
|
T | C | 12 | a0001c0001t0001g0146a0001c0006t0001g0292a0001c0006t0001g0293others(9): Show | 12 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.652-373T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128576450 | ||||||
| chr9:128576606
|
A | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.652-217A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128576606 | ||||||
| chr9:128576719
|
A | G | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.652-104A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 5/56 | chr9 | 128576719 | ||||||
| chr9:128577112
|
G | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.786-17G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 6/56 | chr9 | 128577112 | ||||||
| chr9:128577541
|
T | C | 1 | a0005c0020t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1085+35T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 8/56 | chr9 | 128577541 | ||||||
| chr9:128577576
|
T | TCTTC | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1085+70_1085+71ins others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 8/56 | chr9 | 128577576 | ||||||
| chr9:128577784
|
A | C | 1 | a0002c0004t0002g0275 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1085+278A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 8/56 | chr9 | 128577784 | ||||||
| chr9:128577886
|
T | TG | 161 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1086-220dupG | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 8/56 | INFO_REALIGN_3_PRIME | chr9 | 128577886 | |||||
| chr9:128578027
|
A | G | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1086-83A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 8/56 | chr9 | 128578027 | ||||||
| chr9:128578256
|
C | T | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1221+11C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578256 | ||||||
| chr9:128578360
|
T | A | 1 | a0001c0005t0001g0022 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1221+115T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578360 | ||||||
| chr9:128578360
|
T | C | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1221+115T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578360 | ||||||
| chr9:128578404
|
G | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1221+159G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578404 | ||||||
| chr9:128578450
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0007g0061 | 2 | NA18960.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1221+205G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578450 | ||||||
| chr9:128578483
|
C | T | 1 | a0001c0002t0001g0254 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1221+238C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578483 | ||||||
| chr9:128578490
|
G | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1221+245G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578490 | ||||||
| chr9:128578531
|
T | A | 161 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1221+286T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578531 | ||||||
| chr9:128578566
|
T | C | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1221+321T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578566 | ||||||
| chr9:128578595
|
C | T | 8 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1221+350C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578595 | ||||||
| chr9:128578596
|
T | C | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1221+351T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578596 | ||||||
| chr9:128578672
|
T | C | 111 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(108): Show | 111 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1221+427T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578672 | ||||||
| chr9:128578679
|
G | A | 285 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1221+434G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578679 | ||||||
| chr9:128578810
|
C | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1221+565C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578810 | ||||||
| chr9:128578835
|
GA | G | 148 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1221+609delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | INFO_REALIGN_3_PRIME | chr9 | 128578835 | |||||
| chr9:128578835
|
GAA | G | 115 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0002t0001g0001others(112): Show | 115 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1221+608_1221+609d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | INFO_REALIGN_3_PRIME | chr9 | 128578835 | |||||
| chr9:128578835
|
GAAA | G | 9 | a0001c0002t0001g0187a0001c0007t0001g0007a0001c0007t0001g0008others(6): Show | 9 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1221+607_1221+609d others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | INFO_REALIGN_3_PRIME | chr9 | 128578835 | |||||
| chr9:128578864
|
A | G | 2 | a0001c0014t0003g0018a0001c0014t0003g0019 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1221+619A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128578864 | ||||||
| chr9:128579076
|
A | G | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222-561A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579076 | ||||||
| chr9:128579103
|
G | C | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1222-534G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579103 | ||||||
| chr9:128579182
|
T | C | 11 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(8): Show | 11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222-455T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579182 | ||||||
| chr9:128579363
|
T | C | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1222-274T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579363 | ||||||
| chr9:128579364
|
G | A | 8 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222-273G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579364 | ||||||
| chr9:128579390
|
G | A | 111 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(108): Show | 111 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1222-247G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579390 | ||||||
| chr9:128579411
|
C | G | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222-226C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579411 | ||||||
| chr9:128579445
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222-192A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579445 | ||||||
| chr9:128579542
|
A | G | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1222-95A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 9/56 | chr9 | 128579542 | ||||||
| chr9:128579803
|
A | G | 1 | a0001c0002t0001g0185 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1323+65A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128579803 | ||||||
| chr9:128580039
|
A | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1323+301A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580039 | ||||||
| chr9:128580197
|
C | T | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1323+459C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580197 | ||||||
| chr9:128580393
|
C | G | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1324-529C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580393 | ||||||
| chr9:128580436
|
T | C | 11 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(8): Show | 11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1324-486T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580436 | ||||||
| chr9:128580573
|
T | G | 283 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1324-349T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580573 | ||||||
| chr9:128580579
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0139 | 3 | HG02145.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1324-343G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580579 | ||||||
| chr9:128580862
|
C | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1324-60C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 10/56 | chr9 | 128580862 | ||||||
| chr9:128581474
|
C | CA | 253 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1462-294dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | INFO_REALIGN_3_PRIME | chr9 | 128581474 | |||||
| chr9:128581474
|
C | CAA | 8 | a0001c0001t0001g0038a0001c0001t0001g0105a0001c0002t0001g0186others(5): Show | 8 | HG01981.hp1 HG02135.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1462-295_1462-294d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | INFO_REALIGN_3_PRIME | chr9 | 128581474 | |||||
| chr9:128581474
|
CA | C | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1462-294delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | INFO_REALIGN_3_PRIME | chr9 | 128581474 | |||||
| chr9:128581485
|
A | C | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1462-297A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | chr9 | 128581485 | ||||||
| chr9:128581487
|
AAC | A | 6 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1462-293_1462-292d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | INFO_REALIGN_3_PRIME | chr9 | 128581487 | |||||
| chr9:128581493
|
C | A | 1 | a0001c0016t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1462-289C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | chr9 | 128581493 | ||||||
| chr9:128581718
|
T | C | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1462-64T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | chr9 | 128581718 | ||||||
| chr9:128581755
|
T | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1462-27T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | chr9 | 128581755 | ||||||
| chr9:128581769
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1462-13T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 11/56 | chr9 | 128581769 | ||||||
| chr9:128581927
|
C | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1572+35C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128581927 | ||||||
| chr9:128582035
|
A | G | 2 | a0001c0007t0001g0273a0001c0007t0001g0274 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1572+143A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128582035 | ||||||
| chr9:128582048
|
G | A | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.1572+156G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128582048 | ||||||
| chr9:128582100
|
A | T | 3 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0267 | 3 | HG01884.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1572+208A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128582100 | ||||||
| chr9:128582229
|
G | A | 2 | a0001c0014t0003g0018a0001c0014t0003g0019 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1573-250G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128582229 | ||||||
| chr9:128582299
|
G | A | 310 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1573-180G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128582299 | ||||||
| chr9:128582328
|
GA | G | 283 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1573-145delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | INFO_REALIGN_3_PRIME | chr9 | 128582328 | |||||
| chr9:128582357
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1573-122A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 12/56 | chr9 | 128582357 | ||||||
| chr9:128582590
|
T | C | 1 | a0001c0002t0001g0255 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1650+34T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 13/56 | chr9 | 128582590 | ||||||
| chr9:128582596
|
A | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1650+40A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 13/56 | chr9 | 128582596 | ||||||
| chr9:128582883
|
G | A | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.1806+34G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 14/56 | chr9 | 128582883 | ||||||
| chr9:128583309
|
A | G | 5 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2011+28A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583309 | ||||||
| chr9:128583311
|
G | A | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2011+30G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583311 | ||||||
| chr9:128583312
|
C | A | 1 | a0001c0001t0001g0055 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2011+31C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583312 | ||||||
| chr9:128583375
|
A | G | 7 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2011+94A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583375 | ||||||
| chr9:128583518
|
C | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2011+237C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583518 | ||||||
| chr9:128583520
|
T | C | 6 | a0001c0003t0001g0028a0001c0003t0001g0086a0001c0003t0001g0108others(3): Show | 6 | NA18948.hp2 NA18961.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.2011+239T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583520 | ||||||
| chr9:128583642
|
T | C | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2012-146T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 15/56 | chr9 | 128583642 | ||||||
| chr9:128584193
|
G | A | 4 | a0001c0009t0001g0004a0001c0009t0001g0025a0001c0009t0001g0026others(1): Show | 4 | HG01891.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2194-89G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 16/56 | chr9 | 128584193 | ||||||
| chr9:128584200
|
A | G | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2194-82A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 16/56 | chr9 | 128584200 | ||||||
| chr9:128584216
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2194-66A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 16/56 | chr9 | 128584216 | ||||||
| chr9:128584269
|
T | G | 4 | a0001c0009t0001g0004a0001c0009t0001g0025a0001c0009t0001g0026others(1): Show | 4 | HG01891.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2194-13T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 16/56 | chr9 | 128584269 | ||||||
| chr9:128584879
|
G | A | 3 | a0001c0003t0001g0123a0001c0003t0001g0127a0001c0027t0001g0113 | 3 | HG00408.hp1 HG00609.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.2560+36G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128584879 | ||||||
| chr9:128584886
|
G | A | 294 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.2560+43G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128584886 | ||||||
| chr9:128584890
|
C | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.2560+47C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128584890 | ||||||
| chr9:128585015
|
C | CT | 134 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(131): Show | 134 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.2560+189dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | INFO_REALIGN_3_PRIME | chr9 | 128585015 | |||||
| chr9:128585015
|
C | T | 1 | a0001c0005t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2560+172C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585015 | ||||||
| chr9:128585015
|
CT | C | 7 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0139others(4): Show | 7 | HG02145.hp1 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2560+189delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | INFO_REALIGN_3_PRIME | chr9 | 128585015 | |||||
| chr9:128585173
|
C | G | 1 | a0001c0001t0001g0041 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2560+330C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585173 | ||||||
| chr9:128585286
|
C | T | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.2560+443C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585286 | ||||||
| chr9:128585404
|
C | T | 1 | a0001c0010t0001g0302 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2561-344C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585404 | ||||||
| chr9:128585407
|
A | G | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.2561-341A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585407 | ||||||
| chr9:128585408
|
G | A | 281 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.2561-340G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585408 | ||||||
| chr9:128585492
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2561-256A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585492 | ||||||
| chr9:128585568
|
G | C | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2561-180G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585568 | ||||||
| chr9:128585697
|
G | C | 1 | a0001c0005t0001g0022 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2561-51G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 18/56 | chr9 | 128585697 | ||||||
| chr9:128586033
|
TAGG | T | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2778+71_2778+73del others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | INFO_REALIGN_3_PRIME | chr9 | 128586033 | |||||
| chr9:128586050
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2778+85C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586050 | ||||||
| chr9:128586112
|
G | GT | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG02055.hp2 HG02074.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.2778+172dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | INFO_REALIGN_3_PRIME | chr9 | 128586112 | |||||
| chr9:128586112
|
GT | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0033others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2778+172delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | INFO_REALIGN_3_PRIME | chr9 | 128586112 | |||||
| chr9:128586112
|
GTT | G | 22 | a0001c0001t0001g0032a0001c0002t0001g0181a0001c0002t0001g0211others(19): Show | 22 | HG00735.hp2 HG01069.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.2778+171_2778+172d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | INFO_REALIGN_3_PRIME | chr9 | 128586112 | |||||
| chr9:128586112
|
GTTTTTTT others(3): Show |
G | 4 | a0001c0009t0001g0004a0001c0009t0001g0025a0001c0009t0001g0026others(1): Show | 4 | HG01891.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2778+163_2778+172d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | INFO_REALIGN_3_PRIME | chr9 | 128586112 | |||||
| chr9:128586161
|
C | G | 150 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.2778+196C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586161 | ||||||
| chr9:128586222
|
G | A | 144 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.2778+257G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586222 | ||||||
| chr9:128586330
|
G | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2778+365G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586330 | ||||||
| chr9:128586432
|
C | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2778+467C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586432 | ||||||
| chr9:128586504
|
C | T | 145 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.2778+539C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586504 | ||||||
| chr9:128586506
|
A | G | 1 | a0001c0002t0001g0251 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2778+541A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586506 | ||||||
| chr9:128586617
|
C | T | 1 | a0001c0002t0001g0308 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2778+652C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586617 | ||||||
| chr9:128586644
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2778+679C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586644 | ||||||
| chr9:128586716
|
T | C | 3 | a0001c0002t0001g0219a0001c0002t0001g0220a0001c0002t0001g0222 | 3 | HG02109.hp2 HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2778+751T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586716 | ||||||
| chr9:128586772
|
A | G | 1 | a0001c0007t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2778+807A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586772 | ||||||
| chr9:128586783
|
C | G | 281 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.2778+818C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586783 | ||||||
| chr9:128586822
|
C | CT | 262 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(259): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.2779-773dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | INFO_REALIGN_3_PRIME | chr9 | 128586822 | |||||
| chr9:128586886
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2779-720C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128586886 | ||||||
| chr9:128587100
|
C | T | 1 | a0002c0004t0002g0282 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2779-506C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587100 | ||||||
| chr9:128587111
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2779-495G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587111 | ||||||
| chr9:128587155
|
G | A | 1 | a0001c0002t0001g0178 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2779-451G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587155 | ||||||
| chr9:128587166
|
G | A | 281 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.2779-440G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587166 | ||||||
| chr9:128587272
|
A | G | 1 | a0001c0010t0001g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2779-334A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587272 | ||||||
| chr9:128587434
|
A | G | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2779-172A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587434 | ||||||
| chr9:128587463
|
T | C | 10 | a0001c0002t0001g0180a0001c0002t0001g0185a0001c0002t0001g0219others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2779-143T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587463 | ||||||
| chr9:128587494
|
G | A | 281 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.2779-112G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587494 | ||||||
| chr9:128587515
|
G | C | 1 | a0001c0002t0001g0218 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2779-91G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 19/56 | chr9 | 128587515 | ||||||
| chr9:128587833
|
A | G | 262 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2871+135A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128587833 | ||||||
| chr9:128587838
|
G | GATTT | 5 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0009t0001g0004others(2): Show | 5 | HG01891.hp2 HG03225.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2871+162_2871+165d others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128587838 | |||||
| chr9:128587926
|
A | C | 282 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(279): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.2871+228A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128587926 | ||||||
| chr9:128588013
|
A | AT | 125 | a0001c0001t0001g0103a0001c0001t0001g0133a0001c0002t0001g0001others(122): Show | 125 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2871+331dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588013 | |||||
| chr9:128588013
|
A | ATT | 164 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.2871+330_2871+331d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588013 | |||||
| chr9:128588038
|
G | A | 4 | a0001c0002t0001g0180a0001c0002t0001g0221a0001c0002t0001g0223others(1): Show | 4 | HG02055.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2871+340G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588038 | ||||||
| chr9:128588087
|
TC | T | 3 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009 | 3 | HG01884.hp1 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2871+392delC | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588087 | |||||
| chr9:128588310
|
A | AT | 23 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0007t0001g0007others(20): Show | 23 | HG01884.hp1 HG02040.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.2872-481dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588310 | |||||
| chr9:128588310
|
A | ATT | 16 | a0001c0001t0001g0044a0001c0001t0001g0114a0001c0001t0001g0115others(13): Show | 16 | HG01099.hp2 HG01361.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2872-482_2872-481d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588310 | |||||
| chr9:128588310
|
A | ATTT | 250 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2872-483_2872-481d others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588310 | |||||
| chr9:128588310
|
A | ATTTT | 6 | a0001c0001t0001g0096a0001c0001t0001g0303a0001c0002t0001g0197others(3): Show | 6 | HG01981.hp1 HG02572.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2872-484_2872-481d others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | INFO_REALIGN_3_PRIME | chr9 | 128588310 | |||||
| chr9:128588329
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2872-480G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588329 | ||||||
| chr9:128588330
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2872-479A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588330 | ||||||
| chr9:128588437
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2872-372G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588437 | ||||||
| chr9:128588468
|
C | T | 2 | a0001c0014t0003g0018a0001c0014t0003g0019 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2872-341C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588468 | ||||||
| chr9:128588600
|
C | T | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2872-209C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588600 | ||||||
| chr9:128588763
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2872-46G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588763 | ||||||
| chr9:128588767
|
G | A | 8 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0007t0001g0007others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2872-42G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 20/56 | chr9 | 128588767 | ||||||
| chr9:128588966
|
G | C | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3006+23G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128588966 | ||||||
| chr9:128589012
|
T | C | 2 | a0004c0015t0001g0173a0004c0015t0001g0182 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3006+69T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589012 | ||||||
| chr9:128589043
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3006+100G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589043 | ||||||
| chr9:128589260
|
C | T | 1 | a0001c0002t0005g0227 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3006+317C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589260 | ||||||
| chr9:128589290
|
C | CT | 112 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0001g0051others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.3006+363dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128589290 | |||||
| chr9:128589294
|
T | TC | 13 | a0001c0002t0001g0186a0001c0002t0001g0187a0001c0002t0001g0193others(10): Show | 13 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.3006+351_3006+352i others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589294 | ||||||
| chr9:128589319
|
C | A | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3006+376C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589319 | ||||||
| chr9:128589319
|
C | T | 6 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3006+376C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589319 | ||||||
| chr9:128589337
|
A | G | 277 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.3006+394A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589337 | ||||||
| chr9:128589362
|
C | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122 | 3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3006+419C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589362 | ||||||
| chr9:128589526
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3006+583T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589526 | ||||||
| chr9:128589566
|
G | A | 1 | a0001c0002t0001g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3006+623G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589566 | ||||||
| chr9:128589571
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0007g0061 | 2 | NA18960.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3006+628C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589571 | ||||||
| chr9:128589572
|
G | C | 1 | a0001c0002t0001g0308 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3006+629G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589572 | ||||||
| chr9:128589575
|
CT | C | 26 | a0001c0001t0001g0087a0001c0001t0001g0136a0001c0001t0001g0155others(23): Show | 26 | HG01884.hp1 HG02040.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.3006+650delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128589575 | |||||
| chr9:128589575
|
CTT | C | 268 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.3006+649_3006+650d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128589575 | |||||
| chr9:128589604
|
C | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0133 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3006+661C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589604 | ||||||
| chr9:128589649
|
C | T | 8 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3006+706C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589649 | ||||||
| chr9:128589686
|
C | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3006+743C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589686 | ||||||
| chr9:128589709
|
G | A | 1 | a0001c0002t0001g0255 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3006+766G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589709 | ||||||
| chr9:128589732
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3006+789C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589732 | ||||||
| chr9:128589810
|
C | T | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3006+867C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589810 | ||||||
| chr9:128589822
|
G | A | 1 | a0001c0018t0004g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3006+879G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589822 | ||||||
| chr9:128589844
|
A | G | 294 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.3006+901A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589844 | ||||||
| chr9:128589874
|
C | T | 2 | a0001c0014t0003g0018a0001c0014t0003g0019 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3006+931C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128589874 | ||||||
| chr9:128590182
|
A | G | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3006+1239A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590182 | ||||||
| chr9:128590240
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122 | 3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3007-1237C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590240 | ||||||
| chr9:128590288
|
G | T | 2 | a0001c0014t0003g0018a0001c0014t0003g0019 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3007-1189G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590288 | ||||||
| chr9:128590390
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3007-1087G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590390 | ||||||
| chr9:128590436
|
G | T | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3007-1041G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590436 | ||||||
| chr9:128590547
|
T | TA | 125 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.3007-924dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128590547 | |||||
| chr9:128590547
|
T | TAA | 23 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(20): Show | 23 | HG01891.hp1 HG01981.hp2 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.3007-925_3007-924d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128590547 | |||||
| chr9:128590552
|
AAG | A | 7 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0295others(4): Show | 7 | HG01069.hp1 HG01167.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3007-923_3007-922d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128590552 | |||||
| chr9:128590553
|
AG | A | 15 | a0001c0002t0001g0190a0001c0002t0001g0220a0001c0002t0001g0267others(12): Show | 15 | HG01884.hp1 HG02145.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.3007-923delG | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590553 | ||||||
| chr9:128590554
|
G | A | 271 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.3007-923G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590554 | ||||||
| chr9:128590589
|
C | T | 145 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.3007-888C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590589 | ||||||
| chr9:128590661
|
C | T | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3007-816C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590661 | ||||||
| chr9:128590687
|
TAAAATAC others(3): Show |
T | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3007-784_3007-775d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128590687 | |||||
| chr9:128590756
|
C | T | 145 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.3007-721C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590756 | ||||||
| chr9:128590766
|
A | G | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.3007-711A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590766 | ||||||
| chr9:128590807
|
T | C | 293 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.3007-670T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590807 | ||||||
| chr9:128590841
|
C | T | 1 | a0001c0002t0001g0291 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3007-636C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590841 | ||||||
| chr9:128590864
|
T | C | 1 | a0001c0003t0001g0029 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3007-613T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590864 | ||||||
| chr9:128590882
|
A | C | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3007-595A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590882 | ||||||
| chr9:128590903
|
G | A | 1 | a0005c0020t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3007-574G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590903 | ||||||
| chr9:128590974
|
C | T | 264 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.3007-503C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128590974 | ||||||
| chr9:128591007
|
G | A | 8 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3007-470G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591007 | ||||||
| chr9:128591067
|
CT | C | 281 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.3007-400delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | INFO_REALIGN_3_PRIME | chr9 | 128591067 | |||||
| chr9:128591102
|
C | T | 275 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.3007-375C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591102 | ||||||
| chr9:128591126
|
A | G | 1 | a0001c0017t0006g0012 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3007-351A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591126 | ||||||
| chr9:128591265
|
A | G | 283 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.3007-212A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591265 | ||||||
| chr9:128591288
|
C | G | 283 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.3007-189C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591288 | ||||||
| chr9:128591313
|
G | A | 1 | a0001c0005t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3007-164G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591313 | ||||||
| chr9:128591365
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3007-112C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591365 | ||||||
| chr9:128591438
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0007g0061 | 2 | NA18960.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3007-39G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 21/56 | chr9 | 128591438 | ||||||
| chr9:128591703
|
G | A | 2 | a0001c0009t0001g0004a0001c0009t0001g0025 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3155+78G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128591703 | ||||||
| chr9:128591710
|
G | A | 274 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.3155+85G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128591710 | ||||||
| chr9:128591778
|
G | C | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3155+153G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128591778 | ||||||
| chr9:128591930
|
C | T | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3155+305C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128591930 | ||||||
| chr9:128592182
|
T | G | 2 | a0001c0014t0003g0018a0001c0014t0003g0019 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3155+557T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592182 | ||||||
| chr9:128592266
|
T | C | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3155+641T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592266 | ||||||
| chr9:128592277
|
CT | C | 264 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.3155+667delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | INFO_REALIGN_3_PRIME | chr9 | 128592277 | |||||
| chr9:128592350
|
C | G | 2 | a0001c0002t0001g0226a0001c0002t0001g0260 | 2 | HG00597.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.3156-633C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592350 | ||||||
| chr9:128592461
|
G | C | 9 | a0001c0001t0001g0146a0001c0006t0001g0292a0001c0006t0001g0293others(6): Show | 9 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3156-522G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592461 | ||||||
| chr9:128592602
|
T | C | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3156-381T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592602 | ||||||
| chr9:128592603
|
C | T | 1 | a0001c0017t0006g0012 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3156-380C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592603 | ||||||
| chr9:128592632
|
C | T | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3156-351C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592632 | ||||||
| chr9:128592762
|
C | T | 8 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3156-221C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 22/56 | chr9 | 128592762 | ||||||
| chr9:128593108
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3215+66C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593108 | ||||||
| chr9:128593171
|
T | A | 2 | a0002c0004t0002g0278a0002c0004t0002g0282 | 2 | NA18949.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.3215+129T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593171 | ||||||
| chr9:128593485
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0103 | 2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.3215+443T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593485 | ||||||
| chr9:128593533
|
A | T | 3 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009 | 3 | HG01884.hp1 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3215+491A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593533 | ||||||
| chr9:128593657
|
T | C | 1 | a0001c0014t0003g0018 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3216-518T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593657 | ||||||
| chr9:128593747
|
T | G | 1 | a0001c0002t0001g0229 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3216-428T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593747 | ||||||
| chr9:128593748
|
C | A | 1 | a0001c0002t0001g0229 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3216-427C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 23/56 | chr9 | 128593748 | ||||||
| chr9:128594429
|
A | AT | 15 | a0001c0002t0001g0186a0001c0002t0001g0188a0001c0002t0001g0202others(12): Show | 15 | HG01099.hp2 HG01496.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.3414+77dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594429 | |||||
| chr9:128594429
|
A | ATT | 12 | a0001c0001t0001g0033a0001c0001t0001g0092a0001c0001t0001g0148others(9): Show | 12 | HG02040.hp2 HG02258.hp2 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.3414+76_3414+77dup others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594429 | |||||
| chr9:128594429
|
A | ATTT | 136 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.3414+75_3414+77dup others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594429 | |||||
| chr9:128594429
|
A | ATTTT | 7 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0001g0131others(4): Show | 7 | HG01123.hp2 HG03688.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.3414+74_3414+77dup others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594429 | |||||
| chr9:128594686
|
G | C | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3414+313G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128594686 | ||||||
| chr9:128594708
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3414+335A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128594708 | ||||||
| chr9:128594723
|
C | T | 1 | a0001c0007t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3414+350C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128594723 | ||||||
| chr9:128594804
|
C | CT | 7 | a0001c0001t0001g0064a0001c0001t0001g0107a0001c0001t0001g0125others(4): Show | 7 | HG01243.hp1 HG02109.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.3414+450dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594804 | |||||
| chr9:128594804
|
CT | C | 25 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0068others(22): Show | 25 | HG00280.hp1 HG01256.hp1 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.3414+450delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594804 | |||||
| chr9:128594804
|
CTT | C | 113 | a0001c0001t0001g0131a0001c0002t0001g0001a0001c0002t0001g0002others(110): Show | 113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3414+449_3414+450d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594804 | |||||
| chr9:128594804
|
CTTT | C | 16 | a0001c0002t0001g0176a0001c0002t0001g0210a0001c0002t0001g0218others(13): Show | 16 | HG01069.hp1 HG01167.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.3414+448_3414+450d others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594804 | |||||
| chr9:128594826
|
A | AT | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3414+466dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594826 | |||||
| chr9:128594826
|
AT | A | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3414+466delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128594826 | |||||
| chr9:128594918
|
C | T | 8 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3414+545C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128594918 | ||||||
| chr9:128595065
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3414+692C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595065 | ||||||
| chr9:128595069
|
C | T | 1 | a0001c0002t0001g0209 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3414+696C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595069 | ||||||
| chr9:128595098
|
C | T | 2 | a0001c0002t0001g0174a0001c0002t0001g0204 | 2 | NA18952.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.3414+725C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595098 | ||||||
| chr9:128595105
|
C | T | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3414+732C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595105 | ||||||
| chr9:128595110
|
TCA | T | 116 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(113): Show | 116 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.3414+738_3414+739d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595110 | ||||||
| chr9:128595301
|
G | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0158 | 2 | NA18941.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.3414+928G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595301 | ||||||
| chr9:128595362
|
A | C | 8 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3414+989A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595362 | ||||||
| chr9:128595511
|
T | C | 7 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3414+1138T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595511 | ||||||
| chr9:128595576
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3414+1203G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595576 | ||||||
| chr9:128595689
|
C | T | 8 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3414+1316C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595689 | ||||||
| chr9:128595720
|
C | T | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3414+1347C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595720 | ||||||
| chr9:128595929
|
C | T | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3414+1556C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128595929 | ||||||
| chr9:128596085
|
C | G | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3414+1712C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596085 | ||||||
| chr9:128596133
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3414+1760C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596133 | ||||||
| chr9:128596140
|
G | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3414+1767G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596140 | ||||||
| chr9:128596209
|
A | C | 4 | a0001c0009t0001g0004a0001c0009t0001g0025a0001c0009t0001g0026others(1): Show | 4 | HG01891.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3414+1836A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596209 | ||||||
| chr9:128596299
|
CAG | C | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3414+1929_3414+193 others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128596299 | |||||
| chr9:128596307
|
C | T | 131 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(128): Show | 131 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.3414+1934C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596307 | ||||||
| chr9:128596341
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3414+1968A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596341 | ||||||
| chr9:128596402
|
G | A | 132 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(129): Show | 132 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.3415-1998G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596402 | ||||||
| chr9:128596433
|
C | T | 1 | a0001c0002t0005g0227 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3415-1967C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596433 | ||||||
| chr9:128596497
|
T | C | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1903T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596497 | ||||||
| chr9:128596523
|
G | A | 116 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(113): Show | 116 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.3415-1877G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596523 | ||||||
| chr9:128596528
|
G | A | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3415-1872G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596528 | ||||||
| chr9:128596542
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3415-1858C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596542 | ||||||
| chr9:128596566
|
A | G | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.3415-1834A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596566 | ||||||
| chr9:128596607
|
C | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1793C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596607 | ||||||
| chr9:128596609
|
C | CAAATATA others(9): Show |
2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1791_3415-179 others(20): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596609 | ||||||
| chr9:128596610
|
T | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1790T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596610 | ||||||
| chr9:128596612
|
A | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1788A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596612 | ||||||
| chr9:128596613
|
A | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1787A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596613 | ||||||
| chr9:128596615
|
A | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1785A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596615 | ||||||
| chr9:128596616
|
G | C | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1784G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596616 | ||||||
| chr9:128596617
|
G | C | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1783G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596617 | ||||||
| chr9:128596718
|
G | T | 3 | a0001c0009t0001g0004a0001c0009t0001g0025a0001c0009t0001g0026 | 3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3415-1682G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596718 | ||||||
| chr9:128596755
|
A | G | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3415-1645A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596755 | ||||||
| chr9:128596781
|
C | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1619C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596781 | ||||||
| chr9:128596816
|
G | A | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3415-1584G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596816 | ||||||
| chr9:128596851
|
C | G | 4 | a0001c0002t0001g0188a0001c0002t0001g0202a0001c0002t0001g0203others(1): Show | 4 | HG02451.hp2 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3415-1549C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596851 | ||||||
| chr9:128596946
|
G | T | 1 | a0002c0004t0002g0283 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3415-1454G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596946 | ||||||
| chr9:128596976
|
A | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3415-1424A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596976 | ||||||
| chr9:128596978
|
G | A | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3415-1422G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128596978 | ||||||
| chr9:128597019
|
G | A | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3415-1381G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597019 | ||||||
| chr9:128597110
|
T | C | 151 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.3415-1290T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597110 | ||||||
| chr9:128597191
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3415-1209G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597191 | ||||||
| chr9:128597441
|
T | C | 8 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3415-959T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597441 | ||||||
| chr9:128597454
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3415-946G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597454 | ||||||
| chr9:128597500
|
G | C | 1 | a0001c0002t0001g0232 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3415-900G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597500 | ||||||
| chr9:128597641
|
G | GTTTTGTT others(4): Show |
1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3415-744_3415-734d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | INFO_REALIGN_3_PRIME | chr9 | 128597641 | |||||
| chr9:128597737
|
C | T | 113 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(110): Show | 113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3415-663C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597737 | ||||||
| chr9:128597763
|
G | C | 1 | a0001c0005t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3415-637G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597763 | ||||||
| chr9:128597775
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3415-625C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597775 | ||||||
| chr9:128597806
|
G | A | 9 | a0001c0003t0001g0028a0001c0003t0001g0086a0001c0003t0001g0108others(6): Show | 9 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.3415-594G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597806 | ||||||
| chr9:128597947
|
C | A | 1 | a0001c0002t0001g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3415-453C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597947 | ||||||
| chr9:128597957
|
T | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3415-443T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128597957 | ||||||
| chr9:128598074
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0081a0001c0001t0001g0155 | 3 | NA18967.hp1 NA18979.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.3415-326G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128598074 | ||||||
| chr9:128598092
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3415-308G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128598092 | ||||||
| chr9:128598095
|
T | C | 1 | a0001c0030t0001g0287 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3415-305T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128598095 | ||||||
| chr9:128598168
|
G | A | 1 | a0002c0004t0002g0275 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3415-232G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128598168 | ||||||
| chr9:128598245
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG00280.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3415-155C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128598245 | ||||||
| chr9:128598275
|
T | C | 4 | a0001c0002t0001g0249a0001c0007t0001g0045a0001c0017t0006g0012others(1): Show | 4 | HG01109.hp2 HG01192.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3415-125T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 24/56 | chr9 | 128598275 | ||||||
| chr9:128598530
|
G | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3519+26G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 25/56 | chr9 | 128598530 | ||||||
| chr9:128598749
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3520-214T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 25/56 | chr9 | 128598749 | ||||||
| chr9:128598754
|
A | G | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3520-209A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 25/56 | chr9 | 128598754 | ||||||
| chr9:128598870
|
A | G | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3520-93A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 25/56 | chr9 | 128598870 | ||||||
| chr9:128598949
|
C | G | 1 | a0001c0025t0001g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3520-14C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 25/56 | chr9 | 128598949 | ||||||
| chr9:128599355
|
G | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3543+369G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599355 | ||||||
| chr9:128599391
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0133 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3543+405T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599391 | ||||||
| chr9:128599426
|
T | C | 294 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.3543+440T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599426 | ||||||
| chr9:128599443
|
G | A | 2 | a0002c0004t0002g0278a0002c0004t0002g0282 | 2 | NA18949.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.3543+457G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599443 | ||||||
| chr9:128599479
|
T | A | 1 | a0001c0002t0001g0241 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3543+493T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599479 | ||||||
| chr9:128599482
|
G | GGT | 10 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(7): Show | 10 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.3543+496_3543+497i others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599482 | ||||||
| chr9:128599482
|
G | GT | 142 | a0001c0001t0001g0033a0001c0001t0001g0064a0001c0001t0001g0065others(139): Show | 142 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.3543+509dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599482 | |||||
| chr9:128599482
|
G | GTT | 8 | a0001c0002t0001g0184a0001c0002t0001g0216a0001c0002t0001g0221others(5): Show | 8 | HG02615.hp1 HG02809.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.3543+508_3543+509d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599482 | |||||
| chr9:128599583
|
G | C | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3544-497G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599583 | ||||||
| chr9:128599599
|
G | T | 1 | a0001c0001t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3544-481G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599599 | ||||||
| chr9:128599604
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3544-476G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599604 | ||||||
| chr9:128599633
|
C | T | 1 | a0001c0007t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3544-447C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599633 | ||||||
| chr9:128599685
|
T | TA | 135 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0033others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.3544-374dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599685 | |||||
| chr9:128599685
|
T | TAA | 13 | a0001c0001t0001g0032a0001c0001t0001g0049a0001c0001t0001g0050others(10): Show | 13 | HG01099.hp2 HG01496.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.3544-375_3544-374d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599685 | |||||
| chr9:128599685
|
TA | T | 118 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(115): Show | 118 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.3544-374delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599685 | |||||
| chr9:128599685
|
TAA | T | 17 | a0001c0002t0001g0207a0001c0002t0001g0230a0001c0002t0001g0232others(14): Show | 17 | HG01069.hp1 HG01256.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.3544-375_3544-374d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599685 | |||||
| chr9:128599685
|
TAAAA | T | 10 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(7): Show | 10 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.3544-377_3544-374d others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | INFO_REALIGN_3_PRIME | chr9 | 128599685 | |||||
| chr9:128599686
|
A | T | 3 | a0001c0009t0001g0004a0001c0009t0001g0025a0001c0009t0001g0026 | 3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3544-394A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599686 | ||||||
| chr9:128599710
|
T | C | 1 | a0001c0006t0001g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3544-370T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599710 | ||||||
| chr9:128599788
|
T | G | 1 | a0001c0003t0001g0029 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3544-292T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 26/56 | chr9 | 128599788 | ||||||
| chr9:128600279
|
G | C | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3579+164G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600279 | ||||||
| chr9:128600312
|
G | A | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3579+197G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600312 | ||||||
| chr9:128600340
|
C | T | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3579+225C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600340 | ||||||
| chr9:128600373
|
G | A | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3579+258G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600373 | ||||||
| chr9:128600702
|
ACCCAGGC others(314): Show |
A | 1 | a0001c0001t0001g0042 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3579+611_3579+931d others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600702 | |||||
| chr9:128600809
|
T | C | 7 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3579+694T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600809 | ||||||
| chr9:128600833
|
T | G | 113 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0002t0001g0001others(110): Show | 113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3579+718T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600833 | ||||||
| chr9:128600854
|
G | A | 1 | a0002c0004t0002g0282 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3579+739G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128600854 | ||||||
| chr9:128600974
|
C | CT | 11 | a0001c0002t0001g0030a0001c0005t0001g0015a0001c0005t0001g0017others(8): Show | 11 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.3579+886dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | |||||
| chr9:128600974
|
C | CTT | 10 | a0001c0006t0001g0294a0001c0006t0001g0297a0001c0007t0001g0007others(7): Show | 10 | HG01069.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3579+885_3579+886d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | |||||
| chr9:128600974
|
C | CTTTTTTT others(2): Show |
21 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0048others(18): Show | 21 | HG00099.hp1 HG00408.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.3579+878_3579+886d others(11): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | |||||
| chr9:128600974
|
C | CTTTTTTT others(3): Show |
48 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0033others(45): Show | 48 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.3579+877_3579+886d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | |||||
| chr9:128600974
|
C | CTTTTTTT others(4): Show |
77 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0039others(74): Show | 77 | HG00280.hp2 HG00609.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.3579+876_3579+886d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | |||||
| chr9:128600974
|
C | CTTTTTTT others(5): Show |
43 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0071others(40): Show | 43 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.3579+875_3579+886d others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | |||||
| chr9:128600974
|
C | CTTTTTTT others(6): Show |
34 | a0001c0001t0001g0054a0001c0001t0001g0074a0001c0001t0001g0088others(31): Show | 34 | HG00423.hp1 HG00423.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.3579+874_3579+886d others(15): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | |||||
| chr9:128600974
|
C | CTTTTTTT others(7): Show |
15 | a0001c0001t0001g0137a0001c0001t0001g0155a0001c0001t0001g0286others(12): Show | 15 | HG01109.hp1 HG01891.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.3579+873_3579+886d others(16): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | |||||
| chr9:128600974
|
C | CTTTTTTT others(8): Show |
8 | a0001c0001t0001g0106a0001c0002t0001g0002a0001c0002t0001g0003others(5): Show | 8 | HG00558.hp2 HG01243.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.3579+872_3579+886d others(17): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | |||||
| chr9:128600974
|
C | CTTTTTTT others(10): Show |
2 | a0001c0002t0001g0210a0001c0002t0001g0229 | 2 | NA18967.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3579+870_3579+886d others(19): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | |||||
| chr9:128600974
|
CTTT | C | 9 | a0002c0004t0002g0275a0002c0004t0002g0276a0002c0004t0002g0277others(6): Show | 9 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.3579+884_3579+886d others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | |||||
| chr9:128600974
|
CTTTTTTT others(5): Show |
C | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3579+875_3579+886d others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128600974 | |||||
| chr9:128601015
|
G | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3579+900G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601015 | ||||||
| chr9:128601404
|
A | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3579+1289A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601404 | ||||||
| chr9:128601454
|
T | G | 8 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3579+1339T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601454 | ||||||
| chr9:128601459
|
GCTCACAC others(7): Show |
G | 1 | a0001c0001t0001g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3579+1346_3579+135 others(18): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128601459 | |||||
| chr9:128601460
|
C | T | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3579+1345C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601460 | ||||||
| chr9:128601558
|
CAAATAA | C | 113 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0002t0001g0001others(110): Show | 113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3579+1454_3579+145 others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128601558 | |||||
| chr9:128601640
|
C | T | 3 | a0001c0009t0001g0004a0001c0009t0001g0025a0001c0009t0001g0026 | 3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3579+1525C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601640 | ||||||
| chr9:128601645
|
A | G | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3579+1530A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601645 | ||||||
| chr9:128601704
|
T | C | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3579+1589T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601704 | ||||||
| chr9:128601729
|
C | T | 1 | a0001c0002t0001g0204 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3579+1614C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601729 | ||||||
| chr9:128601732
|
T | C | 295 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.3579+1617T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601732 | ||||||
| chr9:128601960
|
C | A | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3580-1583C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601960 | ||||||
| chr9:128601973
|
G | T | 310 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.3580-1570G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128601973 | ||||||
| chr9:128602053
|
T | A | 1 | a0001c0005t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3580-1490T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602053 | ||||||
| chr9:128602190
|
T | G | 2 | a0001c0007t0001g0045a0005c0020t0001g0006 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3580-1353T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602190 | ||||||
| chr9:128602191
|
T | G | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3580-1352T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602191 | ||||||
| chr9:128602213
|
T | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0143 | 2 | HG03834.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3580-1330T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602213 | ||||||
| chr9:128602221
|
G | GTT | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3580-1310_3580-130 others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128602221 | |||||
| chr9:128602225
|
T | G | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3580-1318T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602225 | ||||||
| chr9:128602287
|
G | T | 37 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0038others(34): Show | 37 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.3580-1256G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602287 | ||||||
| chr9:128602312
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3580-1231G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602312 | ||||||
| chr9:128602313
|
T | G | 1 | a0001c0002t0001g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3580-1230T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602313 | ||||||
| chr9:128602317
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0067 | 2 | NA18939.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.3580-1226A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602317 | ||||||
| chr9:128602463
|
C | T | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3580-1080C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602463 | ||||||
| chr9:128602542
|
G | A | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3580-1001G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602542 | ||||||
| chr9:128602697
|
G | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0080others(3): Show | 6 | NA18954.hp2 NA18964.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.3580-846G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602697 | ||||||
| chr9:128602742
|
T | G | 113 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0002t0001g0001others(110): Show | 113 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.3580-801T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602742 | ||||||
| chr9:128602886
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3580-657T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602886 | ||||||
| chr9:128602897
|
A | G | 1 | a0001c0002t0001g0201 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3580-646A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128602897 | ||||||
| chr9:128602964
|
C | CTACGTTG others(8): Show |
10 | a0001c0002t0001g0230a0002c0004t0001g0285a0002c0004t0002g0275others(7): Show | 10 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.3580-535_3580-521d others(17): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128602964 | |||||
| chr9:128602964
|
CTACGTTG others(8): Show |
C | 4 | a0001c0002t0001g0259a0001c0010t0001g0300a0001c0010t0001g0301others(1): Show | 4 | HG02080.hp2 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3580-535_3580-521d others(17): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | INFO_REALIGN_3_PRIME | chr9 | 128602964 | |||||
| chr9:128603110
|
A | G | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.3580-433A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128603110 | ||||||
| chr9:128603230
|
A | T | 1 | a0001c0001t0001g0043 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3580-313A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128603230 | ||||||
| chr9:128603264
|
C | G | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3580-279C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128603264 | ||||||
| chr9:128603297
|
C | G | 264 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.3580-246C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 27/56 | chr9 | 128603297 | ||||||
| chr9:128603754
|
C | T | 1 | a0001c0007t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3627+164C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128603754 | ||||||
| chr9:128603791
|
G | A | 143 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.3627+201G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128603791 | ||||||
| chr9:128603819
|
C | T | 1 | a0001c0002t0001g0247 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3627+229C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128603819 | ||||||
| chr9:128603902
|
C | T | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3627+312C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128603902 | ||||||
| chr9:128603977
|
G | A | 1 | a0001c0005t0001g0022 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3628-349G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128603977 | ||||||
| chr9:128604127
|
T | C | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3628-199T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128604127 | ||||||
| chr9:128604148
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3628-178A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 28/56 | chr9 | 128604148 | ||||||
| chr9:128604651
|
G | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0081a0001c0001t0001g0155 | 3 | NA18967.hp1 NA18979.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.3719+234G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 29/56 | chr9 | 128604651 | ||||||
| chr9:128604820
|
A | T | 1 | a0001c0001t0001g0156 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3720-214A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 29/56 | chr9 | 128604820 | ||||||
| chr9:128604828
|
G | A | 1 | a0001c0016t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3720-206G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 29/56 | chr9 | 128604828 | ||||||
| chr9:128604907
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3720-127G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 29/56 | chr9 | 128604907 | ||||||
| chr9:128605029
|
T | G | 3 | a0001c0002t0001g0183a0004c0015t0001g0173a0004c0015t0001g0182 | 3 | HG00642.hp1 HG01256.hp2 HG01258.hp1 |
splice_region_variant&intron_variant | LOW | c.3720-5T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 29/56 | chr9 | 128605029 | ||||||
| chr9:128605480
|
A | G | 1 | a0001c0006t0001g0293 | 1 | HG03139.hp1 | splice_region_variant&intron_variant | LOW | c.4046+3A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605480 | ||||||
| chr9:128605579
|
C | T | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4046+102C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605579 | ||||||
| chr9:128605632
|
T | A | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4046+155T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605632 | ||||||
| chr9:128605673
|
A | G | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4046+196A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605673 | ||||||
| chr9:128605718
|
A | G | 302 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.4046+241A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605718 | ||||||
| chr9:128605763
|
G | A | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4046+286G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605763 | ||||||
| chr9:128605764
|
G | A | 1 | a0001c0002t0001g0239 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4046+287G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605764 | ||||||
| chr9:128605851
|
G | T | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4046+374G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605851 | ||||||
| chr9:128605975
|
A | G | 1 | a0001c0023t0001g0306 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4046+498A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128605975 | ||||||
| chr9:128605992
|
CA | C | 148 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.4046+530delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | INFO_REALIGN_3_PRIME | chr9 | 128605992 | |||||
| chr9:128606082
|
G | T | 1 | a0001c0023t0001g0306 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4046+605G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606082 | ||||||
| chr9:128606374
|
C | CAAA | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4046+913_4046+915d others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | INFO_REALIGN_3_PRIME | chr9 | 128606374 | |||||
| chr9:128606374
|
C | CAAAAAAA | 181 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0033others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.4046+909_4046+915d others(9): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | INFO_REALIGN_3_PRIME | chr9 | 128606374 | |||||
| chr9:128606374
|
C | CAAAAAAA others(1): Show |
83 | a0001c0001t0001g0005a0001c0001t0001g0034a0001c0001t0001g0035others(80): Show | 83 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.4046+908_4046+915d others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | INFO_REALIGN_3_PRIME | chr9 | 128606374 | |||||
| chr9:128606374
|
C | CAAAAAAA others(2): Show |
9 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0138others(6): Show | 9 | HG02258.hp2 HG02572.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.4046+907_4046+915d others(11): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | INFO_REALIGN_3_PRIME | chr9 | 128606374 | |||||
| chr9:128606374
|
CAAAAAAA | C | 7 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.4046+909_4046+915d others(9): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | INFO_REALIGN_3_PRIME | chr9 | 128606374 | |||||
| chr9:128606429
|
C | T | 1 | a0001c0006t0001g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4046+952C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606429 | ||||||
| chr9:128606484
|
TA | T | 14 | a0001c0002t0001g0178a0001c0002t0001g0242a0001c0002t0001g0250others(11): Show | 14 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.4046+1008delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606484 | ||||||
| chr9:128606485
|
A | T | 12 | a0001c0002t0001g0031a0001c0009t0001g0004a0001c0009t0001g0025others(9): Show | 12 | HG01891.hp2 HG02040.hp2 HG03516.hp2 others(9): Show |
intron_variant | MODIFIER | c.4046+1008A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606485 | ||||||
| chr9:128606486
|
TA | T | 249 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.4046+1010delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606486 | ||||||
| chr9:128606487
|
A | T | 39 | a0001c0001t0001g0090a0001c0001t0001g0100a0001c0001t0001g0136others(36): Show | 39 | HG00597.hp1 HG01192.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.4046+1010A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606487 | ||||||
| chr9:128606488
|
T | TA | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4046+1011_4046+101 others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606488 | ||||||
| chr9:128606495
|
T | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0136a0001c0001t0001g0150 | 3 | HG00597.hp1 HG01192.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4046+1018T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606495 | ||||||
| chr9:128606496
|
T | G | 17 | a0001c0001t0001g0040a0001c0001t0001g0085a0001c0001t0001g0088others(14): Show | 17 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.4046+1019T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606496 | ||||||
| chr9:128606497
|
T | G | 157 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.4046+1020T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606497 | ||||||
| chr9:128606498
|
G | T | 14 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0097others(11): Show | 14 | HG02040.hp2 HG02647.hp1 HG03471.hp1 others(11): Show |
intron_variant | MODIFIER | c.4046+1021G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606498 | ||||||
| chr9:128606499
|
G | T | 1 | a0002c0004t0002g0278 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4046+1022G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606499 | ||||||
| chr9:128606506
|
A | G | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4046+1029A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606506 | ||||||
| chr9:128606508
|
G | A | 184 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.4046+1031G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606508 | ||||||
| chr9:128606593
|
C | T | 7 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.4047-1011C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606593 | ||||||
| chr9:128606640
|
A | C | 145 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.4047-964A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606640 | ||||||
| chr9:128606692
|
G | A | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4047-912G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606692 | ||||||
| chr9:128606737
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4047-867C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606737 | ||||||
| chr9:128606766
|
G | A | 1 | a0001c0002t0001g0241 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4047-838G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606766 | ||||||
| chr9:128606893
|
C | T | 1 | a0001c0002t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4047-711C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606893 | ||||||
| chr9:128606975
|
C | T | 1 | a0001c0007t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4047-629C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128606975 | ||||||
| chr9:128607026
|
A | G | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4047-578A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607026 | ||||||
| chr9:128607118
|
T | C | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.4047-486T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607118 | ||||||
| chr9:128607179
|
T | C | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4047-425T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607179 | ||||||
| chr9:128607215
|
A | G | 308 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(305): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.4047-389A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607215 | ||||||
| chr9:128607241
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0078 | 2 | NA18953.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.4047-363C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607241 | ||||||
| chr9:128607335
|
G | A | 1 | a0001c0002t0001g0184 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4047-269G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607335 | ||||||
| chr9:128607363
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.4047-241C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607363 | ||||||
| chr9:128607382
|
T | C | 1 | a0002c0004t0002g0278 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4047-222T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607382 | ||||||
| chr9:128607551
|
G | A | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4047-53G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 31/56 | chr9 | 128607551 | ||||||
| chr9:128607723
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4146+20G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 32/56 | chr9 | 128607723 | ||||||
| chr9:128608116
|
C | T | 1 | a0001c0002t0001g0201 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.4345-14C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 33/56 | chr9 | 128608116 | ||||||
| chr9:128608453
|
G | GA | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.4491+177_4491+178i others(3): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/56 | chr9 | 128608453 | ||||||
| chr9:128608477
|
T | C | 268 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.4491+201T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/56 | chr9 | 128608477 | ||||||
| chr9:128608565
|
G | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4491+289G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/56 | chr9 | 128608565 | ||||||
| chr9:128608691
|
A | G | 1 | a0001c0007t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4492-183A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/56 | chr9 | 128608691 | ||||||
| chr9:128608795
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0067 | 2 | NA18939.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.4492-79A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/56 | chr9 | 128608795 | ||||||
| chr9:128608847
|
T | A | 1 | a0001c0002t0001g0225 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4492-27T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 34/56 | chr9 | 128608847 | ||||||
| chr9:128609393
|
G | T | 20 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0087others(17): Show | 20 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.4758+109G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 36/56 | chr9 | 128609393 | ||||||
| chr9:128609549
|
G | T | 1 | a0001c0001t0001g0080 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.4759-102G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 36/56 | chr9 | 128609549 | ||||||
| chr9:128609983
|
C | T | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4773+318C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128609983 | ||||||
| chr9:128609988
|
G | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4773+323G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128609988 | ||||||
| chr9:128610177
|
A | G | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4773+512A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128610177 | ||||||
| chr9:128610332
|
G | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4773+667G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128610332 | ||||||
| chr9:128611326
|
T | C | 302 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.4774-388T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128611326 | ||||||
| chr9:128611427
|
G | A | 1 | a0002c0004t0001g0285 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.4774-287G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128611427 | ||||||
| chr9:128611491
|
A | G | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4774-223A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 37/56 | chr9 | 128611491 | ||||||
| chr9:128611886
|
C | G | 294 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.4905+41C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 38/56 | chr9 | 128611886 | ||||||
| chr9:128612458
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.5043+212A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128612458 | ||||||
| chr9:128612629
|
A | C | 1 | a0001c0002t0001g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5043+383A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128612629 | ||||||
| chr9:128612724
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0147 | 2 | HG01496.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.5043+478G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128612724 | ||||||
| chr9:128612796
|
C | T | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5043+550C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128612796 | ||||||
| chr9:128612924
|
C | CA | 12 | a0001c0002t0001g0249a0002c0004t0001g0285a0002c0004t0002g0275others(9): Show | 12 | HG01192.hp1 HG02040.hp2 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.5044-445dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | INFO_REALIGN_3_PRIME | chr9 | 128612924 | |||||
| chr9:128612937
|
T | A | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5044-444T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128612937 | ||||||
| chr9:128613054
|
G | C | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5044-327G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128613054 | ||||||
| chr9:128613105
|
G | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG00280.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.5044-276G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 39/56 | chr9 | 128613105 | ||||||
| chr9:128613526
|
A | G | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5148+41A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128613526 | ||||||
| chr9:128613554
|
A | G | 1 | a0001c0002t0001g0242 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5148+69A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128613554 | ||||||
| chr9:128613731
|
C | T | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5148+246C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128613731 | ||||||
| chr9:128613802
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5148+317G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128613802 | ||||||
| chr9:128613812
|
C | T | 1 | a0005c0020t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5148+327C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128613812 | ||||||
| chr9:128614077
|
G | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5148+592G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614077 | ||||||
| chr9:128614257
|
C | T | 1 | a0001c0002t0001g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.5148+772C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614257 | ||||||
| chr9:128614265
|
G | C | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5148+780G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614265 | ||||||
| chr9:128614453
|
G | A | 3 | a0001c0009t0001g0004a0001c0009t0001g0025a0001c0009t0001g0026 | 3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.5148+968G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614453 | ||||||
| chr9:128614588
|
TCAAAAAA others(4): Show |
T | 2 | a0001c0001t0001g0040a0001c0001t0001g0150 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.5149-1030_5149-102 others(15): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | INFO_REALIGN_3_PRIME | chr9 | 128614588 | |||||
| chr9:128614609
|
A | C | 5 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.5149-1023A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614609 | ||||||
| chr9:128614610
|
A | C | 16 | a0001c0002t0001g0255a0001c0006t0001g0292a0001c0006t0001g0293others(13): Show | 16 | HG01069.hp1 HG01167.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.5149-1022A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614610 | ||||||
| chr9:128614637
|
G | A | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5149-995G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614637 | ||||||
| chr9:128614832
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5149-800C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614832 | ||||||
| chr9:128614901
|
C | T | 143 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(140): Show | 143 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.5149-731C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614901 | ||||||
| chr9:128614957
|
A | G | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5149-675A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128614957 | ||||||
| chr9:128615047
|
C | G | 1 | a0001c0005t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5149-585C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128615047 | ||||||
| chr9:128615155
|
G | A | 2 | a0001c0007t0001g0045a0005c0020t0001g0006 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5149-477G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128615155 | ||||||
| chr9:128615445
|
G | A | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5149-187G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128615445 | ||||||
| chr9:128615578
|
A | G | 1 | a0001c0002t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5149-54A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 40/56 | chr9 | 128615578 | ||||||
| chr9:128615998
|
C | T | 1 | a0001c0017t0006g0012 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5357+158C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128615998 | ||||||
| chr9:128615999
|
G | A | 1 | a0001c0021t0001g0307 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5357+159G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128615999 | ||||||
| chr9:128616188
|
A | G | 3 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0267 | 3 | HG01884.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.5357+348A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616188 | ||||||
| chr9:128616193
|
T | C | 1 | a0001c0007t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5357+353T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616193 | ||||||
| chr9:128616403
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.5357+563G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616403 | ||||||
| chr9:128616425
|
G | A | 310 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.5357+585G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616425 | ||||||
| chr9:128616611
|
A | G | 1 | a0001c0007t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5357+771A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616611 | ||||||
| chr9:128616640
|
G | A | 12 | a0001c0002t0001g0186a0001c0002t0001g0187a0001c0002t0001g0195others(9): Show | 12 | HG02080.hp1 HG02135.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.5357+800G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616640 | ||||||
| chr9:128616651
|
C | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5357+811C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616651 | ||||||
| chr9:128616681
|
C | T | 3 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009 | 3 | HG01884.hp1 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.5357+841C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616681 | ||||||
| chr9:128616732
|
A | G | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5357+892A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616732 | ||||||
| chr9:128616777
|
T | G | 1 | a0001c0007t0001g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5358-863T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616777 | ||||||
| chr9:128616802
|
C | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5358-838C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616802 | ||||||
| chr9:128616868
|
A | G | 140 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(137): Show | 140 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.5358-772A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616868 | ||||||
| chr9:128616972
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5358-668T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128616972 | ||||||
| chr9:128617162
|
C | T | 7 | a0001c0002t0001g0180a0001c0002t0001g0219a0001c0002t0001g0220others(4): Show | 7 | HG02109.hp2 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.5358-478C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128617162 | ||||||
| chr9:128617265
|
T | A | 1 | a0001c0016t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5358-375T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128617265 | ||||||
| chr9:128617426
|
C | T | 9 | a0001c0005t0001g0022a0001c0006t0001g0293a0001c0006t0001g0296others(6): Show | 9 | HG01109.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5358-214C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128617426 | ||||||
| chr9:128617445
|
A | G | 6 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0006t0001g0298others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.5358-195A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 41/56 | chr9 | 128617445 | ||||||
| chr9:128617793
|
AG | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0303 | 3 | HG02809.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5478+35delG | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/56 | INFO_REALIGN_3_PRIME | chr9 | 128617793 | |||||
| chr9:128617843
|
A | G | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5478+83A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/56 | chr9 | 128617843 | ||||||
| chr9:128617870
|
C | G | 182 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.5478+110C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/56 | chr9 | 128617870 | ||||||
| chr9:128617946
|
A | C | 132 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(129): Show | 132 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.5479-41A>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/56 | chr9 | 128617946 | ||||||
| chr9:128617950
|
G | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5479-37G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 42/56 | chr9 | 128617950 | ||||||
| chr9:128618307
|
T | A | 1 | a0005c0020t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5600+199T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618307 | ||||||
| chr9:128618552
|
C | T | 1 | a0001c0002t0001g0225 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5601-319C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618552 | ||||||
| chr9:128618625
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.5601-246A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618625 | ||||||
| chr9:128618673
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5601-198C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618673 | ||||||
| chr9:128618684
|
C | T | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5601-187C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618684 | ||||||
| chr9:128618704
|
C | T | 1 | a0001c0002t0001g0185 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5601-167C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618704 | ||||||
| chr9:128618715
|
T | C | 295 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.5601-156T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618715 | ||||||
| chr9:128618765
|
G | T | 1 | a0001c0001t0001g0068 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5601-106G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 43/56 | chr9 | 128618765 | ||||||
| chr9:128619038
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5733+35C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619038 | ||||||
| chr9:128619196
|
T | C | 1 | a0001c0002t0001g0305 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.5733+193T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619196 | ||||||
| chr9:128619258
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0063 | 3 | HG00438.hp2 HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.5733+255T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619258 | ||||||
| chr9:128619384
|
C | T | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5733+381C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619384 | ||||||
| chr9:128619458
|
C | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5733+455C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619458 | ||||||
| chr9:128619583
|
C | G | 150 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.5733+580C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619583 | ||||||
| chr9:128619649
|
G | C | 144 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.5733+646G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619649 | ||||||
| chr9:128619663
|
C | G | 102 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0002t0001g0001others(99): Show | 102 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.5733+660C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619663 | ||||||
| chr9:128619678
|
G | T | 19 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(16): Show | 19 | HG01069.hp1 HG01167.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.5733+675G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619678 | ||||||
| chr9:128619735
|
A | G | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5733+732A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619735 | ||||||
| chr9:128619902
|
G | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5733+899G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128619902 | ||||||
| chr9:128620188
|
A | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5734-970A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128620188 | ||||||
| chr9:128620259
|
C | T | 5 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.5734-899C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128620259 | ||||||
| chr9:128620365
|
T | G | 1 | a0001c0005t0001g0022 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5734-793T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128620365 | ||||||
| chr9:128620442
|
T | C | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5734-716T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128620442 | ||||||
| chr9:128620507
|
A | G | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5734-651A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128620507 | ||||||
| chr9:128620724
|
GA | G | 114 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0002t0001g0001others(111): Show | 114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.5734-424delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | INFO_REALIGN_3_PRIME | chr9 | 128620724 | |||||
| chr9:128620724
|
GAA | G | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5734-425_5734-424d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | INFO_REALIGN_3_PRIME | chr9 | 128620724 | |||||
| chr9:128620893
|
G | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0097 | 3 | HG02647.hp1 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.5734-265G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128620893 | ||||||
| chr9:128621025
|
T | C | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5734-133T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 44/56 | chr9 | 128621025 | ||||||
| chr9:128621278
|
G | C | 1 | a0001c0006t0001g0296 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5832+22G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128621278 | ||||||
| chr9:128621587
|
A | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5832+331A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128621587 | ||||||
| chr9:128621587
|
A | T | 1 | a0001c0001t0001g0065 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5832+331A>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128621587 | ||||||
| chr9:128621619
|
A | G | 10 | a0001c0002t0001g0181a0001c0002t0001g0196a0001c0002t0001g0199others(7): Show | 10 | HG01123.hp1 HG01257.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.5832+363A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128621619 | ||||||
| chr9:128621748
|
C | T | 7 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.5832+492C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128621748 | ||||||
| chr9:128622090
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5832+834A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622090 | ||||||
| chr9:128622283
|
G | A | 7 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.5832+1027G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622283 | ||||||
| chr9:128622293
|
C | CT | 122 | a0001c0001t0001g0005a0001c0001t0001g0036a0001c0001t0001g0040others(119): Show | 122 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.5832+1060dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128622293 | |||||
| chr9:128622293
|
C | CTT | 27 | a0001c0001t0001g0136a0001c0002t0001g0001a0001c0002t0001g0184others(24): Show | 27 | HG01109.hp1 HG01257.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.5832+1059_5832+106 others(6): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128622293 | |||||
| chr9:128622323
|
G | T | 1 | a0001c0002t0001g0248 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.5832+1067G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622323 | ||||||
| chr9:128622521
|
A | G | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5832+1265A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622521 | ||||||
| chr9:128622580
|
T | C | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5832+1324T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622580 | ||||||
| chr9:128622601
|
C | T | 1 | a0001c0022t0001g0262 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5832+1345C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622601 | ||||||
| chr9:128622668
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5832+1412C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622668 | ||||||
| chr9:128622669
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5832+1413T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622669 | ||||||
| chr9:128622737
|
G | GTTTA | 17 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(14): Show | 17 | HG02040.hp2 HG02109.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.5832+1509_5832+151 others(8): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128622737 | |||||
| chr9:128622737
|
G | GTTTATTT others(1): Show |
10 | a0001c0002t0001g0242a0001c0006t0001g0292a0001c0006t0001g0293others(7): Show | 10 | HG01069.hp1 HG01109.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.5832+1505_5832+151 others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128622737 | |||||
| chr9:128622944
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.5833-1384G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128622944 | ||||||
| chr9:128623095
|
G | A | 1 | a0001c0003t0001g0029 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.5833-1233G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623095 | ||||||
| chr9:128623177
|
T | TG | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5833-1151_5833-115 others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623177 | ||||||
| chr9:128623178
|
C | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5833-1150C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623178 | ||||||
| chr9:128623179
|
C | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5833-1149C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623179 | ||||||
| chr9:128623239
|
C | CT | 10 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0080others(7): Show | 10 | HG02922.hp2 NA18954.hp2 NA18964.hp1 others(7): Show |
intron_variant | MODIFIER | c.5833-1077dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623239 | |||||
| chr9:128623276
|
T | G | 1 | a0001c0001t0001g0303 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5833-1052T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623276 | ||||||
| chr9:128623424
|
T | C | 12 | a0001c0001t0001g0048a0001c0001t0001g0055a0001c0001t0001g0058others(9): Show | 12 | HG00408.hp2 HG00438.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.5833-904T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623424 | ||||||
| chr9:128623507
|
G | A | 11 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(8): Show | 11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.5833-821G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623507 | ||||||
| chr9:128623622
|
A | AT | 53 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0044others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.5833-684dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623622 | |||||
| chr9:128623622
|
A | ATT | 14 | a0001c0001t0001g0052a0001c0001t0001g0132a0001c0001t0001g0139others(11): Show | 14 | HG01099.hp2 HG01496.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.5833-685_5833-684d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623622 | |||||
| chr9:128623622
|
AT | A | 106 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0156others(103): Show | 106 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.5833-684delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623622 | |||||
| chr9:128623622
|
ATT | A | 6 | a0001c0002t0001g0188a0001c0002t0001g0202a0001c0002t0001g0203others(3): Show | 6 | HG00735.hp1 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.5833-685_5833-684d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623622 | |||||
| chr9:128623622
|
ATTTTTTT others(1): Show |
A | 10 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(7): Show | 10 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.5833-691_5833-684d others(10): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623622 | |||||
| chr9:128623670
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5833-658C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623670 | ||||||
| chr9:128623735
|
G | T | 1 | a0001c0001t0001g0034 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5833-593G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623735 | ||||||
| chr9:128623737
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.5833-591G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623737 | ||||||
| chr9:128623843
|
T | A | 1 | a0001c0016t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5833-485T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623843 | ||||||
| chr9:128623856
|
T | C | 145 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0002t0001g0001others(142): Show | 145 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.5833-472T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623856 | ||||||
| chr9:128623959
|
AT | A | 145 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0002t0001g0001others(142): Show | 145 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.5833-367delT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128623959 | |||||
| chr9:128623975
|
C | T | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5833-353C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128623975 | ||||||
| chr9:128624065
|
G | A | 1 | a0001c0017t0006g0012 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5833-263G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128624065 | ||||||
| chr9:128624086
|
C | CA | 63 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0037others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.5833-216dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | |||||
| chr9:128624086
|
C | CAA | 11 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0074others(8): Show | 11 | HG01192.hp2 HG01981.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.5833-217_5833-216d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | |||||
| chr9:128624086
|
CA | C | 15 | a0001c0001t0001g0055a0001c0001t0001g0126a0001c0003t0001g0029others(12): Show | 15 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.5833-216delA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | |||||
| chr9:128624086
|
CAA | C | 8 | a0002c0004t0002g0275a0002c0004t0002g0277a0002c0004t0002g0278others(5): Show | 8 | HG02040.hp2 HG03688.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.5833-217_5833-216d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | |||||
| chr9:128624086
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0266 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5833-225_5833-216d others(12): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | |||||
| chr9:128624086
|
CAAAAAAA others(4): Show |
C | 112 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0002t0001g0001others(109): Show | 112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.5833-226_5833-216d others(13): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | |||||
| chr9:128624086
|
CAAAAAAA others(5): Show |
C | 6 | a0001c0002t0001g0210a0001c0007t0001g0007a0001c0007t0001g0008others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.5833-227_5833-216d others(14): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | INFO_REALIGN_3_PRIME | chr9 | 128624086 | |||||
| chr9:128624166
|
G | A | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5833-162G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 45/56 | chr9 | 128624166 | ||||||
| chr9:128624569
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5992+82G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 46/56 | chr9 | 128624569 | ||||||
| chr9:128624739
|
CATA | C | 4 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(1): Show | 4 | NA18948.hp1 NA18960.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.5992+255_5992+257d others(5): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 46/56 | INFO_REALIGN_3_PRIME | chr9 | 128624739 | |||||
| chr9:128624820
|
C | G | 1 | a0001c0017t0006g0012 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5993-283C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 46/56 | chr9 | 128624820 | ||||||
| chr9:128624840
|
G | A | 1 | a0001c0001t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5993-263G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 46/56 | chr9 | 128624840 | ||||||
| chr9:128625012
|
C | CA | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.5993-85dupA | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 46/56 | INFO_REALIGN_3_PRIME | chr9 | 128625012 | |||||
| chr9:128625599
|
C | T | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.6070-170C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 47/56 | chr9 | 128625599 | ||||||
| chr9:128625628
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6070-141T>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 47/56 | chr9 | 128625628 | ||||||
| chr9:128626045
|
G | C | 1 | a0001c0007t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6279+67G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 48/56 | chr9 | 128626045 | ||||||
| chr9:128626292
|
G | A | 1 | a0001c0021t0001g0307 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6280-99G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 48/56 | chr9 | 128626292 | ||||||
| chr9:128626295
|
T | C | 11 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(8): Show | 11 | HG02040.hp2 HG03669.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.6280-96T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 48/56 | chr9 | 128626295 | ||||||
| chr9:128626364
|
C | T | 145 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.6280-27C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 48/56 | chr9 | 128626364 | ||||||
| chr9:128626781
|
C | CAA | 308 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(305): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.6576+94_6576+95ins others(2): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626781 | ||||||
| chr9:128626817
|
T | C | 4 | a0001c0009t0001g0004a0001c0009t0001g0025a0001c0009t0001g0026others(1): Show | 4 | HG01891.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.6576+130T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626817 | ||||||
| chr9:128626817
|
T | TC | 15 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(12): Show | 15 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.6576+131dupC | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | INFO_REALIGN_3_PRIME | chr9 | 128626817 | |||||
| chr9:128626838
|
A | G | 10 | a0002c0004t0001g0285a0002c0004t0002g0275a0002c0004t0002g0276others(7): Show | 10 | HG03669.hp2 HG03688.hp1 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.6576+151A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626838 | ||||||
| chr9:128626880
|
C | A | 15 | a0001c0002t0001g0030a0001c0009t0001g0004a0001c0009t0001g0025others(12): Show | 15 | HG01891.hp2 HG02040.hp2 HG03516.hp2 others(12): Show |
intron_variant | MODIFIER | c.6576+193C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626880 | ||||||
| chr9:128626897
|
C | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0067 | 2 | NA18939.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.6576+210C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626897 | ||||||
| chr9:128626915
|
G | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.6576+228G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626915 | ||||||
| chr9:128626936
|
T | C | 112 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0002t0001g0001others(109): Show | 112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.6576+249T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626936 | ||||||
| chr9:128626971
|
C | T | 2 | a0001c0001t0001g0035a0001c0002t0001g0196 | 2 | HG01123.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.6576+284C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128626971 | ||||||
| chr9:128627125
|
TTC | T | 3 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009 | 3 | HG01884.hp1 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.6577-259_6577-258d others(4): Show |
SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | INFO_REALIGN_3_PRIME | chr9 | 128627125 | |||||
| chr9:128627195
|
C | T | 1 | a0001c0002t0001g0175 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6577-191C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128627195 | ||||||
| chr9:128627202
|
G | C | 1 | a0001c0002t0001g0223 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6577-184G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128627202 | ||||||
| chr9:128627241
|
C | T | 2 | a0001c0007t0001g0045a0005c0020t0001g0006 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.6577-145C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128627241 | ||||||
| chr9:128627265
|
C | T | 121 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0002t0001g0001others(118): Show | 121 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.6577-121C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 49/56 | chr9 | 128627265 | ||||||
| chr9:128627515
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | NA18984.hp1 NA18990.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.6689+17G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 50/56 | chr9 | 128627515 | ||||||
| chr9:128627515
|
G | C | 1 | a0001c0002t0001g0230 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6689+17G>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 50/56 | chr9 | 128627515 | ||||||
| chr9:128627517
|
C | G | 1 | a0001c0002t0001g0230 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6689+19C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 50/56 | chr9 | 128627517 | ||||||
| chr9:128627662
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.6689+164G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 50/56 | chr9 | 128627662 | ||||||
| chr9:128628060
|
A | G | 6 | a0001c0008t0001g0167a0001c0008t0001g0168a0001c0008t0001g0169others(3): Show | 6 | HG01099.hp2 HG01496.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.6707+118A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628060 | ||||||
| chr9:128628081
|
G | A | 5 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.6707+139G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628081 | ||||||
| chr9:128628096
|
G | T | 1 | a0001c0026t0001g0198 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6707+154G>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628096 | ||||||
| chr9:128628162
|
G | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.6707+220G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628162 | ||||||
| chr9:128628193
|
C | A | 126 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0002t0001g0001others(123): Show | 126 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.6707+251C>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628193 | ||||||
| chr9:128628261
|
G | A | 1 | a0001c0002t0001g0218 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.6707+319G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628261 | ||||||
| chr9:128628326
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6707+384G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628326 | ||||||
| chr9:128628362
|
T | C | 3 | a0001c0010t0001g0300a0001c0010t0001g0301a0001c0010t0001g0302 | 3 | HG02615.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6707+420T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628362 | ||||||
| chr9:128628369
|
G | A | 144 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.6707+427G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628369 | ||||||
| chr9:128628561
|
G | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.6707+619G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628561 | ||||||
| chr9:128628563
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.6707+621C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628563 | ||||||
| chr9:128628751
|
A | G | 1 | a0001c0002t0001g0249 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6707+809A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628751 | ||||||
| chr9:128628844
|
C | G | 1 | a0001c0010t0001g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6707+902C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628844 | ||||||
| chr9:128628923
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6707+981C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128628923 | ||||||
| chr9:128629016
|
G | A | 1 | a0001c0007t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6707+1074G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629016 | ||||||
| chr9:128629096
|
T | C | 1 | a0002c0004t0002g0283 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.6707+1154T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629096 | ||||||
| chr9:128629139
|
G | A | 1 | a0001c0002t0001g0305 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.6708-1182G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629139 | ||||||
| chr9:128629284
|
G | A | 8 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(5): Show | 8 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.6708-1037G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629284 | ||||||
| chr9:128629322
|
C | T | 4 | a0001c0006t0001g0292a0001c0006t0001g0294a0001c0006t0001g0295others(1): Show | 4 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.6708-999C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629322 | ||||||
| chr9:128629366
|
C | T | 1 | a0002c0004t0002g0278 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.6708-955C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629366 | ||||||
| chr9:128629506
|
T | C | 301 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(298): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.6708-815T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629506 | ||||||
| chr9:128629541
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6708-780C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629541 | ||||||
| chr9:128629558
|
C | T | 1 | a0001c0022t0001g0262 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6708-763C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629558 | ||||||
| chr9:128629569
|
G | A | 1 | a0001c0002t0001g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6708-752G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629569 | ||||||
| chr9:128629579
|
G | A | 3 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009 | 3 | HG01884.hp1 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.6708-742G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629579 | ||||||
| chr9:128629617
|
C | T | 1 | a0001c0002t0001g0181 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6708-704C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629617 | ||||||
| chr9:128629707
|
C | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0134 | 3 | HG00140.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.6708-614C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629707 | ||||||
| chr9:128629795
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0128a0001c0001t0001g0304 | 3 | HG02071.hp2 NA18951.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.6708-526A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629795 | ||||||
| chr9:128629804
|
C | T | 1 | a0001c0002t0001g0244 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.6708-517C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629804 | ||||||
| chr9:128629828
|
G | A | 1 | a0001c0017t0006g0012 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6708-493G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128629828 | ||||||
| chr9:128630077
|
C | T | 11 | a0001c0006t0001g0292a0001c0006t0001g0293a0001c0006t0001g0294others(8): Show | 11 | HG01069.hp1 HG01167.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.6708-244C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128630077 | ||||||
| chr9:128630168
|
C | T | 1 | a0001c0002t0001g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.6708-153C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128630168 | ||||||
| chr9:128630243
|
C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0074others(4): Show | 7 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.6708-78C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128630243 | ||||||
| chr9:128630274
|
G | A | 270 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.6708-47G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128630274 | ||||||
| chr9:128630314
|
C | T | 12 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0005t0001g0013others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.6708-7C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 51/56 | chr9 | 128630314 | ||||||
| chr9:128630568
|
C | T | 1 | a0001c0025t0001g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6762+193C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128630568 | ||||||
| chr9:128630625
|
G | GT | 310 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.6762+251dupT | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | INFO_REALIGN_3_PRIME | chr9 | 128630625 | |||||
| chr9:128630638
|
C | T | 1 | a0001c0002t0001g0217 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.6762+263C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128630638 | ||||||
| chr9:128630648
|
C | G | 1 | a0001c0016t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6762+273C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128630648 | ||||||
| chr9:128630663
|
T | G | 296 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.6762+288T>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128630663 | ||||||
| chr9:128630693
|
A | G | 1 | a0002c0004t0002g0283 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.6762+318A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128630693 | ||||||
| chr9:128630980
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0119 | 2 | HG00741.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.6762+605A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128630980 | ||||||
| chr9:128631103
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.6762+728C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631103 | ||||||
| chr9:128631224
|
G | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6762+849G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631224 | ||||||
| chr9:128631369
|
G | A | 5 | a0001c0007t0001g0007a0001c0007t0001g0008a0001c0007t0001g0009others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.6763-758G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631369 | ||||||
| chr9:128631582
|
T | C | 1 | a0001c0002t0001g0256 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6763-545T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631582 | ||||||
| chr9:128631655
|
G | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6763-472G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631655 | ||||||
| chr9:128631776
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0138 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6763-351C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631776 | ||||||
| chr9:128631777
|
G | A | 5 | a0001c0005t0001g0013a0001c0005t0001g0014a0001c0005t0001g0015others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.6763-350G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631777 | ||||||
| chr9:128631873
|
T | C | 1 | a0001c0006t0001g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6763-254T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631873 | ||||||
| chr9:128631880
|
C | T | 1 | a0001c0002t0001g0194 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.6763-247C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631880 | ||||||
| chr9:128631946
|
A | G | 1 | a0001c0001t0007g0061 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.6763-181A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128631946 | ||||||
| chr9:128632016
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.6763-111C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128632016 | ||||||
| chr9:128632018
|
A | G | 261 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.6763-109A>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128632018 | ||||||
| chr9:128632083
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0078 | 2 | NA18953.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.6763-44G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128632083 | ||||||
| chr9:128632095
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.6763-32C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 52/56 | chr9 | 128632095 | ||||||
| chr9:128632541
|
C | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0138a0001c0025t0001g0179 | 3 | HG02572.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.7014-31C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 54/56 | chr9 | 128632541 | ||||||
| chr9:128632556
|
C | T | 1 | a0001c0003t0001g0111 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.7014-16C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 54/56 | chr9 | 128632556 | ||||||
| chr9:128632756
|
C | G | 1 | a0001c0002t0001g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.7160+38C>G | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 55/56 | chr9 | 128632756 | ||||||
| chr9:128632800
|
G | A | 1 | a0001c0002t0001g0291 | 1 | HG00735.hp1 | splice_region_variant&intron_variant | LOW | c.7161-8G>A | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 55/56 | chr9 | 128632800 | ||||||
| chr9:128632985
|
T | C | 1 | a0001c0007t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.7308+30T>C | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 56/56 | chr9 | 128632985 | ||||||
| chr9:128633005
|
C | T | 1 | a0001c0016t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7308+50C>T | SPTAN1 | ENSG00000197694.19 | transcript | ENST00000372739.7 | protein_coding | 56/56 | chr9 | 128633005 |