Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84501 |
|---|---|
| ensemblid | ENSG00000204991.11 |
| hgncid | 30623 |
| symbol | SPIRE2 |
| name | spire type actin nucleation factor 2 |
| refseq_nuc | NM_032451.2 |
| refseq_prot | NP_115827.1 |
| ensembl_nuc | ENST00000378247.8 |
| ensembl_prot | ENSP00000367494.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 89828475 |
| end | 89871319 |
| strand | + |
| ver | v1.2 |
| region | chr16:89828475-89871319 |
| region5000 | chr16:89823475-89876319 |
| regionname0 | SPIRE2_chr16_89828475_89871319 |
| regionname5000 | SPIRE2_chr16_89823475_89876319 |
| 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 | 714 | 292 | 89 | 65 | 84 | 15 | 37 | 66 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0002 | 0/0 | 337 | 23 | 0 | 0 | 20 | 1 | 2 | 9 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0003 | 0/0 | 714 | 12 | 0 | 5 | 1 | 0 | 6 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0004 | 0/0 | 714 | 12 | 0 | 0 | 11 | 0 | 1 | 7 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0005 | 0/0 | 715 | 5 | 0 | 1 | 4 | 0 | 0 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0006 | 0/0 | 714 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0007 | 0/0 | 714 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0008 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0009 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0010 | 0/0 | 714 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0011 | 0/0 | 714 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0012 | 0/0 | 714 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0013 | 0/0 | 714 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0014 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0015 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0016 | 0/0 | 344 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2145 | 256 | 84 | 57 | 72 | 14 | 28 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0002 | 0/0 | 2240 | 23 | 0 | 0 | 20 | 1 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0003 | 0/1 | 2145 | 16 | 0 | 4 | 7 | 1 | 3 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0004 | 0/0 | 2145 | 12 | 0 | 0 | 11 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0005 | 0/0 | 2145 | 12 | 0 | 5 | 1 | 0 | 6 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0006 | 0/0 | 2145 | 6 | 0 | 0 | 4 | 0 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0007 | 0/0 | 2148 | 4 | 0 | 1 | 3 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0008 | 0/0 | 2145 | 4 | 2 | 2 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0009 | 0/0 | 2145 | 3 | 0 | 0 | 0 | 0 | 3 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0010 | 0/0 | 2145 | 2 | 2 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0011 | 0/0 | 2145 | 2 | 2 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0012 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0013 | 0/0 | 2240 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0014 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0015 | 0/0 | 2194 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0016 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0017 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0018 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0019 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0020 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0021 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0022 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0023 | 0/0 | 2237 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0024 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0025 | 0/0 | 2240 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0026 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| c0027 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1124 | 279 | 76 | 59 | 86 | 15 | 42 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0002 | 0/0 | 1119 | 32 | 0 | 1 | 28 | 1 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0003 | 0/0 | 1118 | 20 | 19 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0004 | 0/0 | 1124 | 11 | 0 | 6 | 5 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0005 | 0/1 | 1124 | 4 | 0 | 0 | 3 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0006 | 0/0 | 1124 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0007 | 0/0 | 1124 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0008 | 0/0 | 1124 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0009 | 0/0 | 1125 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0010 | 0/0 | 1124 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0011 | 0/0 | 1124 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0012 | 0/0 | 1124 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0013 | 0/0 | 1124 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0014 | 0/0 | 1119 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| t0015 | 0/0 | 1124 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| 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 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0273 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2145 | 256 | 84 | 57 | 72 | 14 | 28 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0003 | 0/1 | 2145 | 16 | 0 | 4 | 7 | 1 | 3 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0006 | 0/0 | 2145 | 6 | 0 | 0 | 4 | 0 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0008 | 0/0 | 2145 | 4 | 2 | 2 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0009 | 0/0 | 2145 | 3 | 0 | 0 | 0 | 0 | 3 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0011 | 0/0 | 2145 | 2 | 2 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0012 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0018 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0019 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0021 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0027 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0002c0002 | 0/0 | 2240 | 23 | 0 | 0 | 20 | 1 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0003c0005 | 0/0 | 2145 | 12 | 0 | 5 | 1 | 0 | 6 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0004c0004 | 0/0 | 2145 | 12 | 0 | 0 | 11 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0005c0007 | 0/0 | 2148 | 4 | 0 | 1 | 3 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0005c0014 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0006c0010 | 0/0 | 2145 | 2 | 2 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0007c0026 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0008c0013 | 0/0 | 2240 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0009c0025 | 0/0 | 2240 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0010c0016 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0011c0022 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0012c0017 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0013c0020 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0014c0024 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0015c0023 | 0/0 | 2237 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0016c0015 | 0/0 | 2194 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3268 | 217 | 65 | 47 | 64 | 14 | 26 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0001t0002 | 0/0 | 3263 | 2 | 0 | 0 | 2 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0001t0003 | 0/0 | 3262 | 20 | 19 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0001t0004 | 0/0 | 3268 | 11 | 0 | 6 | 5 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0001t0006 | 0/0 | 3268 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0001t0007 | 0/0 | 3268 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0001t0009 | 0/0 | 3269 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0001t0010 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0001t0011 | 0/0 | 3268 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0001t0015 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0003t0001 | 0/0 | 3268 | 12 | 0 | 3 | 5 | 1 | 3 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0003t0005 | 0/1 | 3268 | 3 | 0 | 0 | 2 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0003t0013 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0006t0001 | 0/0 | 3268 | 6 | 0 | 0 | 4 | 0 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0008t0001 | 0/0 | 3268 | 4 | 2 | 2 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0009t0001 | 0/0 | 3268 | 3 | 0 | 0 | 0 | 0 | 3 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0011t0001 | 0/0 | 3268 | 2 | 2 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0012t0005 | 0/0 | 3268 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0018t0012 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0019t0001 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0021t0001 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0001c0027t0001 | 0/0 | 3268 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0002c0002t0002 | 0/0 | 3358 | 22 | 0 | 0 | 19 | 1 | 2 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0002c0002t0014 | 0/0 | 3358 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0003c0005t0001 | 0/0 | 3268 | 12 | 0 | 5 | 1 | 0 | 6 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0004c0004t0001 | 0/0 | 3268 | 12 | 0 | 0 | 11 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0005c0007t0002 | 0/0 | 3266 | 4 | 0 | 1 | 3 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0005c0014t0002 | 0/0 | 3266 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0006c0010t0001 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0006c0010t0008 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0007c0026t0001 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0008c0013t0002 | 0/0 | 3358 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0009c0025t0002 | 0/0 | 3358 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0010c0016t0001 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0011c0022t0001 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0012c0017t0001 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0013c0020t0001 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0014c0024t0001 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0015c0023t0001 | 0/0 | 3360 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| a0016c0015t0002 | 0/0 | 3312 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | copy fasta | chr16 | 89823475 | 89876319 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0009g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0010g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0011g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0001t0015g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0005g0273 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0003t0013g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0006t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0006t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0006t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0006t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0006t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0006t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0008t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0008t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0008t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0008t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0009t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0009t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0009t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0011t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0011t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0012t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0018t0012g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0019t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0021t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0001c0027t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0002c0002t0014g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0005t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0005t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0005t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0005t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0005t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0005t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0005t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0005t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0005t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0005t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0005t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0003c0005t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0004t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0004c0004t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0005c0007t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0005c0007t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0005c0007t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0005c0007t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0005c0014t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0006c0010t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0006c0010t0008g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0007c0026t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0008c0013t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0009c0025t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0010c0016t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0011c0022t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0012c0017t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0013c0020t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0014c0024t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0015c0023t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| a0016c0015t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | GBR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | GBR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0302 | EUR | GBR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0274 | EUR | FIN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0303 | EUR | FIN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0023 | EUR | FIN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0349 | EUR | FIN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00408 | hp1 | a0004 | c0004 | t0001 | g0173 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00621 | hp1 | a0005 | c0014 | t0002 | g0021 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00741 | hp1 | a0003 | c0005 | t0001 | g0300 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01081 | hp1 | a0001 | c0008 | t0001 | g0009 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01099 | hp1 | a0001 | c0021 | t0001 | g0065 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01099 | hp2 | a0001 | c0001 | t0010 | g0348 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01106 | hp2 | a0003 | c0005 | t0001 | g0301 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01167 | hp1 | a0003 | c0005 | t0001 | g0296 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01167 | hp2 | a0001 | c0008 | t0001 | g0011 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0224 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01169 | hp1 | a0003 | c0005 | t0001 | g0298 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01175 | hp1 | a0005 | c0007 | t0002 | g0036 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0340 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01243 | hp1 | a0001 | c0018 | t0012 | g0346 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01256 | hp1 | a0001 | c0001 | t0015 | g0229 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0262 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0289 | EUR | IBS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | IBS | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01884 | hp1 | a0013 | c0020 | t0001 | g0073 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01928 | hp1 | a0011 | c0022 | t0001 | g0255 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0127 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01943 | hp1 | a0001 | c0003 | t0013 | g0128 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0315 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0133 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01993 | hp1 | a0003 | c0005 | t0001 | g0297 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0230 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0316 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02015 | hp2 | a0004 | c0004 | t0001 | g0197 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02040 | hp2 | a0002 | c0002 | t0014 | g0044 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02071 | hp1 | a0003 | c0005 | t0001 | g0295 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02071 | hp2 | a0014 | c0024 | t0001 | g0270 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02074 | hp2 | a0004 | c0004 | t0001 | g0186 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02080 | hp1 | a0005 | c0007 | t0002 | g0052 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0278 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | KHV | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0331 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | CDX | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0325 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0132 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0326 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0330 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0174 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | PEL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02451 | hp2 | a0006 | c0010 | t0008 | g0313 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02572 | hp2 | a0001 | c0008 | t0001 | g0010 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02602 | hp1 | a0003 | c0005 | t0001 | g0309 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02602 | hp2 | a0001 | c0001 | t0011 | g0217 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0320 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0341 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02698 | hp1 | a0003 | c0005 | t0001 | g0299 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0338 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0334 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0336 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0323 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02896 | hp1 | a0001 | c0011 | t0001 | g0319 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0333 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02897 | hp1 | a0001 | c0011 | t0001 | g0318 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02922 | hp2 | a0012 | c0017 | t0001 | g0148 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03041 | hp1 | a0001 | c0008 | t0001 | g0008 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0344 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0342 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03139 | hp1 | a0001 | c0019 | t0001 | g0317 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03139 | hp2 | a0007 | c0026 | t0001 | g0146 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0343 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03239 | hp2 | a0001 | c0006 | t0001 | g0016 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03490 | hp2 | a0001 | c0006 | t0001 | g0015 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0025 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0335 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0350 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03669 | hp2 | a0001 | c0009 | t0001 | g0018 | SAS | PJL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03688 | hp2 | a0003 | c0005 | t0001 | g0311 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03831 | hp2 | a0001 | c0027 | t0001 | g0020 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0070 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03927 | hp2 | a0004 | c0004 | t0001 | g0195 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0121 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04115 | hp1 | a0001 | c0009 | t0001 | g0019 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04184 | hp1 | a0003 | c0005 | t0001 | g0310 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04204 | hp1 | a0001 | c0009 | t0001 | g0017 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04204 | hp2 | a0003 | c0005 | t0001 | g0312 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0165 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG04228 | hp2 | a0003 | c0005 | t0001 | g0304 | SAS | STU | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | YRI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18612 | hp1 | a0008 | c0013 | t0002 | g0033 | EAS | CHB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18747 | hp1 | a0004 | c0004 | t0001 | g0196 | EAS | CHB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0329 | AFR | YRI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18939 | hp2 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18943 | hp1 | a0009 | c0025 | t0002 | g0039 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18945 | hp1 | a0004 | c0004 | t0001 | g0355 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18951 | hp2 | a0001 | c0006 | t0001 | g0012 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18970 | hp1 | a0004 | c0004 | t0001 | g0194 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0103 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18977 | hp1 | a0001 | c0012 | t0005 | g0272 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18979 | hp1 | a0001 | c0006 | t0001 | g0013 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18983 | hp2 | a0001 | c0003 | t0005 | g0275 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18984 | hp2 | a0005 | c0007 | t0002 | g0032 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18990 | hp1 | a0016 | c0015 | t0002 | g0049 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18995 | hp2 | a0004 | c0004 | t0001 | g0211 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18998 | hp1 | a0004 | c0004 | t0001 | g0205 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA18998 | hp2 | a0001 | c0003 | t0001 | g0277 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19030 | hp1 | a0010 | c0016 | t0001 | g0005 | AFR | LWK | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19054 | hp1 | a0004 | c0004 | t0001 | g0356 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19057 | hp1 | a0001 | c0006 | t0001 | g0014 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19060 | hp2 | a0004 | c0004 | t0001 | g0271 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19065 | hp2 | a0001 | c0003 | t0005 | g0276 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0102 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19067 | hp2 | a0004 | c0004 | t0001 | g0187 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19070 | hp1 | a0005 | c0007 | t0002 | g0041 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0345 | AFR | YRI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | TSI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0354 | EUR | TSI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | GIH | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0120 | SAS | GIH | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0339 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG03471 | hp2 | a0015 | c0023 | t0001 | g0055 | AFR | MSL | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | USA | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | USA | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | USA | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | USA | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0332 | AFR | LWK | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| NA21309 | hp2 | a0006 | c0010 | t0001 | g0314 | AFR | LWK | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0005 | g0273 | REF | REF | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0098 | REF | REF | SPIRE2_chr16_89823475_89876319 | SPIRE2 | chr16 | 89823475 | 89876319 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89828561
|
C | A | 1 | a0006 | 2 | HG02451.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.11C>A | p.Ala4Glu | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 87/3268 | 11/2145 | 4/714 | chr16 | 89828561 | ||
| chr16:89828590
|
G | A | 1 | a0004 | 12 | HG00408.hp1 HG02015.hp2 HG02074.hp2 others(9): Show |
missense_variant | MODERATE | c.40G>A | p.Ala14Thr | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 116/3268 | 40/2145 | 14/714 | chr16 | 89828590 | ||
| chr16:89828705
|
G | T | 1 | a0007 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.155G>T | p.Arg52Leu | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 231/3268 | 155/2145 | 52/714 | chr16 | 89828705 | ||
| chr16:89845339
|
G | A | 1 | a0008 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.262G>A | p.Val88Met | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/15 | 338/3268 | 262/2145 | 88/714 | chr16 | 89845339 | ||
| chr16:89850383
|
C | T | 1 | a0009 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.368C>T | p.Pro123Leu | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/15 | 444/3268 | 368/2145 | 123/714 | chr16 | 89850383 | ||
| chr16:89850471
|
C | CGAG | 5 | a0002a0005a0008others(2): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
disruptive_inframe_insertion | MODERATE | c.470_472dupAGG | p.Glu157dup | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/15 | 549/3268 | 473/2145 | 158/714 | INFO_REALIGN_3_PRIME | chr16 | 89850471 | |
| chr16:89850607
|
G | A | 1 | a0010 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.592G>A | p.Val198Met | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/15 | 668/3268 | 592/2145 | 198/714 | chr16 | 89850607 | ||
| chr16:89856144
|
C | T | 1 | a0011 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.1010C>T | p.Pro337Leu | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/15 | 1086/3268 | 1010/2145 | 337/714 | chr16 | 89856144 | ||
| chr16:89859195
|
C | G | 1 | a0013 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1303C>G | p.Leu435Val | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/15 | 1379/3268 | 1303/2145 | 435/714 | chr16 | 89859195 | ||
| chr16:89859283
|
C | A | 1 | a0012 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1391C>A | p.Pro464Gln | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/15 | 1467/3268 | 1391/2145 | 464/714 | chr16 | 89859283 | ||
| chr16:89860743
|
C | T | 1 | a0003 | 12 | HG00741.hp1 HG01106.hp2 HG01167.hp1 others(9): Show |
missense_variant | MODERATE | c.1523C>T | p.Ser508Leu | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/15 | 1599/3268 | 1523/2145 | 508/714 | chr16 | 89860743 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89828586
|
G | A | 2 | a0001c0003a0001c0012 | 17 | HG00280.hp1 HG01928.hp2 HG01943.hp1 others(14): Show |
synonymous_variant | LOW | c.36G>A | p.Ala12Ala | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 112/3268 | 36/2145 | 12/714 | chr16 | 89828586 | ||
| chr16:89828592
|
A | G | 5 | a0001c0006a0001c0008a0001c0009others(2): Show | 16 | HG01081.hp1 HG01167.hp2 HG02451.hp2 others(13): Show |
synonymous_variant | LOW | c.42A>G | p.Ala14Ala | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 118/3268 | 42/2145 | 14/714 | chr16 | 89828592 | ||
| chr16:89828601
|
G | C | 1 | a0001c0011 | 2 | HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.51G>C | p.Pro17Pro | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 127/3268 | 51/2145 | 17/714 | chr16 | 89828601 | ||
| chr16:89828655
|
C | G | 1 | a0001c0012 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.105C>G | p.Leu35Leu | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/15 | 181/3268 | 105/2145 | 35/714 | chr16 | 89828655 | ||
| chr16:89854309
|
C | T | 1 | a0001c0009 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
synonymous_variant | LOW | c.669C>T | p.Asp223Asp | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 4/15 | 745/3268 | 669/2145 | 223/714 | chr16 | 89854309 | ||
| chr16:89854549
|
A | G | 8 | a0002c0002a0005c0007a0005c0014others(5): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
synonymous_variant | LOW | c.789A>G | p.Gln263Gln | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/15 | 865/3268 | 789/2145 | 263/714 | chr16 | 89854549 | ||
| chr16:89854585
|
G | A | 1 | a0005c0014 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.825G>A | p.Gln275Gln | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/15 | 901/3268 | 825/2145 | 275/714 | chr16 | 89854585 | ||
| chr16:89856208
|
G | A | 1 | a0001c0008 | 4 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(1): Show |
synonymous_variant | LOW | c.1074G>A | p.Pro358Pro | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/15 | 1150/3268 | 1074/2145 | 358/714 | chr16 | 89856208 | ||
| chr16:89858453
|
C | T | 1 | a0001c0021 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.1218C>T | p.Arg406Arg | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/15 | 1294/3268 | 1218/2145 | 406/714 | chr16 | 89858453 | ||
| chr16:89859281
|
C | G | 1 | a0001c0027 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.1389C>G | p.Pro463Pro | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/15 | 1465/3268 | 1389/2145 | 463/714 | chr16 | 89859281 | ||
| chr16:89860696
|
G | A | 1 | a0015c0023 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.1476G>A | p.Ala492Ala | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/15 | 1552/3268 | 1476/2145 | 492/714 | chr16 | 89860696 | ||
| chr16:89870104
|
C | T | 1 | a0001c0019 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.1977C>T | p.Tyr659Tyr | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 2053/3268 | 1977/2145 | 659/714 | chr16 | 89870104 | ||
| chr16:89870182
|
G | A | 1 | a0001c0018 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.2055G>A | p.Lys685Lys | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 2131/3268 | 2055/2145 | 685/714 | chr16 | 89870182 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89870394
|
C | T | 2 | a0001c0003t0005a0001c0012t0005 | 4 | NA18977.hp1 NA18983.hp2 NA19065.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*122C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 122 | chr16 | 89870394 | |||||
| chr16:89870446
|
C | T | 1 | a0001c0001t0015 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*174C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 174 | chr16 | 89870446 | |||||
| chr16:89870508
|
G | C | 1 | a0001c0001t0006 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 236 | chr16 | 89870508 | |||||
| chr16:89870549
|
C | T | 1 | a0002c0002t0014 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 277 | chr16 | 89870549 | |||||
| chr16:89870618
|
G | A | 1 | a0001c0001t0007 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*346G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 346 | chr16 | 89870618 | |||||
| chr16:89870679
|
C | T | 1 | a0001c0003t0013 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*407C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 407 | chr16 | 89870679 | |||||
| chr16:89870762
|
C | T | 1 | a0001c0018t0012 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*490C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 490 | chr16 | 89870762 | |||||
| chr16:89870818
|
G | A | 1 | a0006c0010t0008 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*546G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 546 | chr16 | 89870818 | |||||
| chr16:89871029
|
T | G | 2 | a0001c0001t0004a0001c0001t0015 | 12 | HG01168.hp2 HG01169.hp2 HG01256.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*757T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 757 | chr16 | 89871029 | |||||
| chr16:89871086
|
G | GA | 9 | a0001c0001t0002a0001c0001t0009a0002c0002t0002others(6): Show | 34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*825dupA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 826 | INFO_REALIGN_3_PRIME | chr16 | 89871086 | ||||
| chr16:89871102
|
C | T | 1 | a0001c0001t0011 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*830C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 830 | chr16 | 89871102 | |||||
| chr16:89871118
|
CTGCCCT | C | 9 | a0001c0001t0002a0001c0001t0003a0002c0002t0002others(6): Show | 53 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*854_*859delGCCCTT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 854 | INFO_REALIGN_3_PRIME | chr16 | 89871118 | ||||
| chr16:89871237
|
G | C | 1 | a0001c0001t0010 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*965G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 15/15 | 965 | chr16 | 89871237 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89828863
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.244+69G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89828863 | ||||||
| chr16:89828864
|
G | T | 1 | a0001c0001t0001g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.244+70G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89828864 | ||||||
| chr16:89829027
|
C | T | 2 | a0004c0004t0001g0355a0004c0004t0001g0356 | 2 | NA18945.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.244+233C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829027 | ||||||
| chr16:89829061
|
G | T | 9 | a0001c0001t0001g0347a0001c0001t0001g0349a0001c0001t0001g0350others(6): Show | 9 | HG00323.hp2 HG00733.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+267G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829061 | ||||||
| chr16:89829081
|
G | C | 1 | a0001c0001t0001g0002 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.244+287G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829081 | ||||||
| chr16:89829108
|
T | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0010c0016t0001g0005 | 3 | HG03486.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.244+314T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829108 | ||||||
| chr16:89829114
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.244+320G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829114 | ||||||
| chr16:89829140
|
C | T | 28 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0324others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.244+346C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829140 | ||||||
| chr16:89829143
|
T | C | 28 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0324others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.244+349T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829143 | ||||||
| chr16:89829184
|
C | T | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+390C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829184 | ||||||
| chr16:89829201
|
G | T | 2 | a0001c0001t0004g0315a0001c0001t0004g0316 | 2 | HG01943.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.244+407G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829201 | ||||||
| chr16:89829377
|
C | T | 2 | a0006c0010t0001g0314a0006c0010t0008g0313 | 2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.244+583C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829377 | ||||||
| chr16:89829453
|
G | A | 14 | a0001c0006t0001g0007a0001c0006t0001g0012a0001c0006t0001g0013others(11): Show | 14 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.244+659G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829453 | ||||||
| chr16:89829545
|
T | C | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.244+751T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829545 | ||||||
| chr16:89829597
|
C | G | 35 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(32): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.244+803C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829597 | ||||||
| chr16:89829649
|
GGTGGGGG others(2326): Show |
G | 1 | a0001c0001t0001g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.244+856_244+3188de others(1): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829649 | ||||||
| chr16:89829721
|
C | G | 1 | a0001c0001t0001g0002 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.244+927C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829721 | ||||||
| chr16:89829812
|
T | C | 36 | a0001c0001t0002g0051a0001c0001t0007g0026a0001c0019t0001g0317others(33): Show | 36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.244+1018T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829812 | ||||||
| chr16:89829835
|
C | T | 33 | a0001c0001t0002g0051a0001c0001t0007g0026a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+1041C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829835 | ||||||
| chr16:89829923
|
C | A | 33 | a0001c0001t0002g0051a0001c0001t0007g0026a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+1129C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829923 | ||||||
| chr16:89829924
|
A | C | 8 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(5): Show | 8 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.244+1130A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829924 | ||||||
| chr16:89829925
|
T | G | 2 | a0001c0001t0001g0054a0015c0023t0001g0055 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.244+1131T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89829925 | ||||||
| chr16:89830015
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(285): Show | 288 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.244+1221A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830015 | ||||||
| chr16:89830034
|
T | C | 2 | a0001c0011t0001g0318a0001c0011t0001g0319 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.244+1240T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830034 | ||||||
| chr16:89830073
|
C | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(247): Show | 250 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.244+1279C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830073 | ||||||
| chr16:89830105
|
G | C | 2 | a0001c0001t0001g0054a0015c0023t0001g0055 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.244+1311G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830105 | ||||||
| chr16:89830269
|
G | C | 1 | a0001c0001t0001g0099 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.244+1475G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830269 | ||||||
| chr16:89830416
|
C | T | 4 | a0003c0005t0001g0309a0003c0005t0001g0310a0003c0005t0001g0311others(1): Show | 4 | HG02602.hp1 HG03688.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+1622C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830416 | ||||||
| chr16:89830426
|
G | A | 34 | a0001c0001t0002g0051a0001c0001t0007g0026a0001c0019t0001g0317others(31): Show | 34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.244+1632G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830426 | ||||||
| chr16:89830503
|
A | T | 7 | a0001c0003t0001g0274a0001c0003t0001g0277a0001c0003t0001g0278others(4): Show | 7 | HG00280.hp1 HG02080.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.244+1709A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830503 | ||||||
| chr16:89830524
|
T | C | 36 | a0001c0001t0002g0051a0001c0001t0007g0026a0001c0019t0001g0317others(33): Show | 36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.244+1730T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830524 | ||||||
| chr16:89830617
|
A | G | 1 | a0002c0002t0002g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.244+1823A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830617 | ||||||
| chr16:89830652
|
G | A | 354 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(351): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.244+1858G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830652 | ||||||
| chr16:89830741
|
C | A | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(299): Show | 302 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.244+1947C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830741 | ||||||
| chr16:89830744
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.244+1950T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830744 | ||||||
| chr16:89830866
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0099others(110): Show | 113 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.244+2072C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830866 | ||||||
| chr16:89830908
|
C | CT | 6 | a0001c0009t0001g0017a0001c0009t0001g0018a0001c0009t0001g0019others(3): Show | 6 | HG00323.hp1 HG03669.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.244+2133dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89830908 | |||||
| chr16:89830908
|
C | CTT | 31 | a0001c0001t0002g0051a0001c0001t0007g0026a0001c0019t0001g0317others(28): Show | 31 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.244+2132_244+2133d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89830908 | |||||
| chr16:89830908
|
CTT | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(236): Show | 239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.244+2132_244+2133d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89830908 | |||||
| chr16:89830908
|
CTTT | C | 8 | a0001c0001t0001g0104a0001c0001t0001g0167a0001c0001t0001g0288others(5): Show | 8 | HG01516.hp1 HG02615.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+2131_244+2133d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89830908 | |||||
| chr16:89830948
|
T | C | 34 | a0001c0001t0002g0051a0001c0001t0007g0026a0001c0019t0001g0317others(31): Show | 34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.244+2154T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830948 | ||||||
| chr16:89830949
|
G | T | 34 | a0001c0001t0002g0051a0001c0001t0007g0026a0001c0019t0001g0317others(31): Show | 34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.244+2155G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830949 | ||||||
| chr16:89830967
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(284): Show | 287 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.244+2173C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830967 | ||||||
| chr16:89830974
|
A | G | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+2180A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830974 | ||||||
| chr16:89830983
|
C | T | 2 | a0006c0010t0001g0314a0006c0010t0008g0313 | 2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.244+2189C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830983 | ||||||
| chr16:89830987
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG00597.hp1 NA18971.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+2193G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89830987 | ||||||
| chr16:89831036
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0099others(110): Show | 113 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.244+2242A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831036 | ||||||
| chr16:89831046
|
A | T | 2 | a0006c0010t0001g0314a0006c0010t0008g0313 | 2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.244+2252A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831046 | ||||||
| chr16:89831064
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.244+2270C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831064 | ||||||
| chr16:89831066
|
C | A | 15 | a0001c0001t0003g0345a0001c0006t0001g0007a0001c0006t0001g0012others(12): Show | 15 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.244+2272C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831066 | ||||||
| chr16:89831071
|
G | A | 15 | a0001c0001t0003g0345a0001c0006t0001g0007a0001c0006t0001g0012others(12): Show | 15 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.244+2277G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831071 | ||||||
| chr16:89831111
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.244+2317G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831111 | ||||||
| chr16:89831217
|
T | C | 1 | a0002c0002t0002g0024 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.244+2423T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831217 | ||||||
| chr16:89831394
|
T | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | NA18949.hp1 NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.244+2600T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831394 | ||||||
| chr16:89831399
|
C | CT | 8 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0305others(5): Show | 8 | HG01109.hp1 HG01123.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.244+2621dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89831399 | |||||
| chr16:89831399
|
CT | C | 13 | a0001c0001t0001g0054a0001c0001t0001g0169a0001c0001t0001g0279others(10): Show | 13 | HG00323.hp1 HG00621.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.244+2621delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89831399 | |||||
| chr16:89831482
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(222): Show | 225 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.244+2688T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831482 | ||||||
| chr16:89831488
|
A | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(222): Show | 225 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.244+2694A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831488 | ||||||
| chr16:89831490
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(222): Show | 225 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.244+2696T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831490 | ||||||
| chr16:89831498
|
C | T | 1 | a0001c0003t0001g0165 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.244+2704C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831498 | ||||||
| chr16:89831522
|
C | T | 33 | a0001c0001t0002g0051a0001c0001t0007g0026a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+2728C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831522 | ||||||
| chr16:89831546
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.244+2752C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831546 | ||||||
| chr16:89831556
|
C | A | 5 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0003g0325others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+2762C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831556 | ||||||
| chr16:89831633
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(299): Show | 302 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.244+2839A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831633 | ||||||
| chr16:89831644
|
A | G | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0014c0024t0001g0270 | 3 | HG02071.hp2 HG03927.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.244+2850A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831644 | ||||||
| chr16:89831776
|
C | T | 2 | a0006c0010t0001g0314a0006c0010t0008g0313 | 2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.244+2982C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831776 | ||||||
| chr16:89831783
|
T | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(287): Show | 290 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.244+2989T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831783 | ||||||
| chr16:89831848
|
T | A | 1 | a0001c0001t0001g0171 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.244+3054T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831848 | ||||||
| chr16:89831883
|
A | G | 8 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(5): Show | 8 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.244+3089A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831883 | ||||||
| chr16:89831922
|
C | T | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0095others(24): Show | 27 | HG01081.hp1 HG01167.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.244+3128C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831922 | ||||||
| chr16:89831965
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.244+3171C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831965 | ||||||
| chr16:89831968
|
G | A | 1 | a0001c0003t0001g0101 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.244+3174G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831968 | ||||||
| chr16:89831984
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.244+3190G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89831984 | ||||||
| chr16:89832059
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.244+3265C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832059 | ||||||
| chr16:89832202
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.244+3408G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832202 | ||||||
| chr16:89832203
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.244+3409T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832203 | ||||||
| chr16:89832250
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.244+3456C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832250 | ||||||
| chr16:89832252
|
C | T | 34 | a0001c0001t0002g0051a0001c0001t0007g0026a0001c0019t0001g0317others(31): Show | 34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.244+3458C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832252 | ||||||
| chr16:89832342
|
A | G | 2 | a0001c0001t0001g0054a0015c0023t0001g0055 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.244+3548A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832342 | ||||||
| chr16:89832356
|
G | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(284): Show | 287 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.244+3562G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832356 | ||||||
| chr16:89832374
|
A | C | 1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.244+3580A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832374 | ||||||
| chr16:89832647
|
T | C | 33 | a0001c0001t0002g0051a0001c0001t0007g0026a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+3853T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832647 | ||||||
| chr16:89832748
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.244+3954C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832748 | ||||||
| chr16:89832808
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.244+4014G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832808 | ||||||
| chr16:89832835
|
T | G | 2 | a0001c0001t0001g0113a0004c0004t0001g0173 | 2 | HG00408.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.244+4041T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832835 | ||||||
| chr16:89832981
|
C | T | 1 | a0003c0005t0001g0304 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.244+4187C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832981 | ||||||
| chr16:89832989
|
TTTC | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(231): Show | 234 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.244+4198_244+4200d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89832989 | |||||
| chr16:89832990
|
TTC | T | 51 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(48): Show | 51 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.244+4198_244+4199d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89832990 | |||||
| chr16:89832991
|
TC | T | 13 | a0001c0001t0001g0164a0001c0001t0003g0345a0001c0006t0001g0012others(10): Show | 13 | HG01081.hp1 HG01167.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.244+4198delC | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832991 | ||||||
| chr16:89832992
|
C | T | 2 | a0001c0006t0001g0016a0001c0027t0001g0020 | 2 | HG03239.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.244+4198C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89832992 | ||||||
| chr16:89833007
|
G | T | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(301): Show | 304 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.244+4213G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833007 | ||||||
| chr16:89833060
|
A | G | 2 | a0006c0010t0001g0314a0006c0010t0008g0313 | 2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.244+4266A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833060 | ||||||
| chr16:89833354
|
A | C | 1 | a0001c0003t0001g0278 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.244+4560A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833354 | ||||||
| chr16:89833532
|
C | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(249): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.244+4738C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833532 | ||||||
| chr16:89833627
|
A | G | 2 | a0001c0001t0001g0351a0001c0001t0001g0352 | 2 | HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.244+4833A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833627 | ||||||
| chr16:89833671
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.244+4877C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833671 | ||||||
| chr16:89833681
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.244+4887C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833681 | ||||||
| chr16:89833763
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.244+4969G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833763 | ||||||
| chr16:89833787
|
G | A | 33 | a0001c0001t0002g0051a0001c0001t0007g0026a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+4993G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833787 | ||||||
| chr16:89833829
|
C | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(248): Show | 251 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.244+5035C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833829 | ||||||
| chr16:89833893
|
A | G | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+5099A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833893 | ||||||
| chr16:89833974
|
G | C | 1 | a0001c0001t0001g0305 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.244+5180G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89833974 | ||||||
| chr16:89834087
|
C | T | 36 | a0001c0001t0002g0051a0001c0001t0007g0026a0001c0019t0001g0317others(33): Show | 36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.244+5293C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834087 | ||||||
| chr16:89834088
|
GCTCGCGG others(587): Show |
G | 33 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+5319_244+5912d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834088 | |||||
| chr16:89834092
|
G | A | 36 | a0001c0001t0002g0051a0001c0001t0007g0026a0001c0019t0001g0317others(33): Show | 36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.244+5298G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834092 | ||||||
| chr16:89834092
|
GCGGTTGG others(125): Show |
G | 1 | a0001c0008t0001g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.244+5357_244+5488d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834092 | |||||
| chr16:89834094
|
G | A | 33 | a0001c0001t0002g0051a0001c0001t0007g0026a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+5300G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834094 | ||||||
| chr16:89834129
|
C | T | 9 | a0001c0001t0003g0320a0001c0001t0003g0323a0001c0001t0003g0338others(6): Show | 9 | HG01192.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.244+5335C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834129 | ||||||
| chr16:89834157
|
C | T | 1 | a0001c0001t0007g0026 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.244+5363C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834157 | ||||||
| chr16:89834179
|
CTGGATAA others(59): Show |
C | 3 | a0001c0003t0001g0101a0001c0003t0001g0102a0001c0003t0001g0103 | 3 | NA18970.hp2 NA19054.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.244+5423_244+5488d others(68): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834179 | |||||
| chr16:89834280
|
G | C | 1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.244+5486G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834280 | ||||||
| chr16:89834301
|
T | C | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.244+5507T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834301 | ||||||
| chr16:89834317
|
A | G | 1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.244+5523A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834317 | ||||||
| chr16:89834357
|
C | T | 3 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0265 | 3 | HG02027.hp1 HG02083.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.244+5563C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834357 | ||||||
| chr16:89834358
|
G | A | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.244+5564G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834358 | ||||||
| chr16:89834366
|
G | GTCGTAGA others(59): Show |
1 | a0001c0001t0001g0279 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.244+5648_244+5713d others(68): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834366 | |||||
| chr16:89834366
|
GTCGTAGA others(59): Show |
G | 1 | a0001c0001t0001g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.244+5648_244+5713d others(68): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834366 | |||||
| chr16:89834368
|
CGTAGAAG others(257): Show |
C | 1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.244+5638_244+5901d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834368 | |||||
| chr16:89834400
|
A | T | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+5606A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834400 | ||||||
| chr16:89834421
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094 | 3 | HG00642.hp2 HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.244+5627C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834421 | ||||||
| chr16:89834432
|
ATCGTAGA others(257): Show |
A | 1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.244+5828_244+6091d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834432 | |||||
| chr16:89834460
|
G | A | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01071.hp1 HG02735.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+5666G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834460 | ||||||
| chr16:89834468
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.244+5674C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834468 | ||||||
| chr16:89834488
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.244+5694G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834488 | ||||||
| chr16:89834527
|
T | A | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+5733T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834527 | ||||||
| chr16:89834551
|
T | C | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.244+5757T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834551 | ||||||
| chr16:89834564
|
G | A | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+5770G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834564 | ||||||
| chr16:89834574
|
G | C | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.244+5780G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834574 | ||||||
| chr16:89834575
|
C | G | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.244+5781C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834575 | ||||||
| chr16:89834576
|
C | T | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.244+5782C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834576 | ||||||
| chr16:89834577
|
C | G | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.244+5783C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834577 | ||||||
| chr16:89834578
|
C | G | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.244+5784C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834578 | ||||||
| chr16:89834578
|
CATAAGCA others(59): Show |
C | 2 | a0001c0001t0001g0100a0001c0001t0009g0174 | 2 | HG02293.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.244+5838_244+5903d others(68): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834578 | |||||
| chr16:89834630
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.244+5836G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834630 | ||||||
| chr16:89834632
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0003t0001g0120others(1): Show | 4 | HG02723.hp2 HG02965.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+5838T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834632 | ||||||
| chr16:89834698
|
C | A | 1 | a0001c0001t0001g0266 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.244+5904C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834698 | ||||||
| chr16:89834707
|
C | G | 15 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0337others(12): Show | 15 | HG01109.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.244+5913C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834707 | ||||||
| chr16:89834748
|
A | G | 1 | a0001c0001t0001g0350 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.244+5954A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834748 | ||||||
| chr16:89834762
|
A | G | 4 | a0001c0001t0001g0350a0002c0002t0002g0025a0002c0002t0002g0050others(1): Show | 4 | HG00621.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+5968A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834762 | ||||||
| chr16:89834775
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.244+5981G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834775 | ||||||
| chr16:89834788
|
C | A | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | HG02451.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+5994C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834788 | ||||||
| chr16:89834790
|
A | ATGTGAAT others(59): Show |
1 | a0001c0001t0001g0324 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.244+6021_244+6086d others(68): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89834790 | |||||
| chr16:89834790
|
A | G | 3 | a0002c0002t0002g0025a0002c0002t0002g0050a0005c0014t0002g0021 | 3 | HG00621.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.244+5996A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834790 | ||||||
| chr16:89834820
|
G | A | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.244+6026G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834820 | ||||||
| chr16:89834830
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.244+6036C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834830 | ||||||
| chr16:89834886
|
A | G | 9 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(6): Show | 9 | HG01256.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+6092A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834886 | ||||||
| chr16:89834910
|
C | T | 33 | a0001c0001t0002g0051a0001c0001t0007g0026a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+6116C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834910 | ||||||
| chr16:89834952
|
G | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG01358.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.244+6158G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834952 | ||||||
| chr16:89834954
|
C | T | 1 | a0001c0008t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.244+6160C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834954 | ||||||
| chr16:89834988
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0177a0001c0001t0001g0178others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+6194G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89834988 | ||||||
| chr16:89835016
|
GCGGTTGG others(125): Show |
G | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.244+6281_244+6412d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89835016 | |||||
| chr16:89835039
|
GGATAAGC others(59): Show |
G | 4 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0321others(1): Show | 4 | HG02965.hp1 HG03516.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+6288_244+6353d others(68): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89835039 | |||||
| chr16:89835105
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.244+6311A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835105 | ||||||
| chr16:89835175
|
AAGCATAG others(70): Show |
A | 11 | a0001c0001t0001g0001a0001c0001t0001g0104a0001c0001t0001g0152others(8): Show | 11 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.244+6382_244+6458d others(79): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835175 | ||||||
| chr16:89835210
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.244+6416G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835210 | ||||||
| chr16:89835264
|
G | C | 1 | a0010c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244+6470G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835264 | ||||||
| chr16:89835350
|
C | T | 14 | a0001c0006t0001g0007a0001c0006t0001g0012a0001c0006t0001g0013others(11): Show | 14 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.244+6556C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835350 | ||||||
| chr16:89835359
|
G | A | 33 | a0001c0001t0002g0051a0001c0001t0007g0026a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.244+6565G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835359 | ||||||
| chr16:89835374
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.244+6580C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835374 | ||||||
| chr16:89835821
|
T | G | 1 | a0001c0001t0001g0182 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.244+7027T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835821 | ||||||
| chr16:89835828
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.244+7034G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89835828 | ||||||
| chr16:89836074
|
T | C | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(303): Show | 306 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.244+7280T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836074 | ||||||
| chr16:89836132
|
G | A | 2 | a0006c0010t0001g0314a0006c0010t0008g0313 | 2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.244+7338G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836132 | ||||||
| chr16:89836233
|
C | G | 2 | a0001c0011t0001g0318a0001c0011t0001g0319 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.244+7439C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836233 | ||||||
| chr16:89836274
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.244+7480A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836274 | ||||||
| chr16:89836346
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.244+7552G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836346 | ||||||
| chr16:89836358
|
A | C | 20 | a0001c0001t0001g0058a0001c0001t0001g0327a0001c0001t0001g0328others(17): Show | 20 | HG01081.hp1 HG01167.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.244+7564A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836358 | ||||||
| chr16:89836430
|
C | A | 1 | a0001c0001t0001g0183 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.244+7636C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836430 | ||||||
| chr16:89836456
|
A | G | 1 | a0001c0003t0001g0165 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.244+7662A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836456 | ||||||
| chr16:89836576
|
C | T | 1 | a0001c0001t0003g0336 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.244+7782C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836576 | ||||||
| chr16:89836777
|
C | G | 1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.244+7983C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836777 | ||||||
| chr16:89836818
|
G | GA | 63 | a0001c0001t0001g0006a0001c0001t0001g0059a0001c0001t0001g0099others(60): Show | 63 | HG00408.hp1 HG00408.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.244+8038dupA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89836818 | |||||
| chr16:89836833
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.244+8039G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836833 | ||||||
| chr16:89836834
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.244+8040A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836834 | ||||||
| chr16:89836885
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.244+8091C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836885 | ||||||
| chr16:89836927
|
G | A | 1 | a0004c0004t0001g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.244+8133G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89836927 | ||||||
| chr16:89837008
|
A | C | 32 | a0001c0019t0001g0317a0002c0002t0002g0022a0002c0002t0002g0023others(29): Show | 32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.244+8214A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837008 | ||||||
| chr16:89837094
|
G | A | 10 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0003g0325others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.245-8228G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837094 | ||||||
| chr16:89837143
|
C | T | 8 | a0001c0001t0001g0104a0001c0006t0001g0007a0001c0006t0001g0012others(5): Show | 8 | HG02895.hp2 HG03239.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-8179C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837143 | ||||||
| chr16:89837144
|
G | A | 37 | a0001c0001t0001g0112a0001c0001t0001g0124a0001c0001t0001g0125others(34): Show | 37 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.245-8178G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837144 | ||||||
| chr16:89837213
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.245-8109C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837213 | ||||||
| chr16:89837247
|
C | T | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-8075C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837247 | ||||||
| chr16:89837272
|
C | T | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-8050C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837272 | ||||||
| chr16:89837320
|
C | T | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-8002C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837320 | ||||||
| chr16:89837415
|
A | T | 1 | a0001c0001t0001g0002 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.245-7907A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837415 | ||||||
| chr16:89837435
|
G | A | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-7887G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837435 | ||||||
| chr16:89837582
|
G | T | 2 | a0001c0011t0001g0318a0001c0011t0001g0319 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.245-7740G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837582 | ||||||
| chr16:89837781
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-7541C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837781 | ||||||
| chr16:89837787
|
A | G | 20 | a0001c0001t0001g0104a0001c0001t0001g0135a0001c0001t0001g0136others(17): Show | 20 | HG01891.hp2 HG02145.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.245-7535A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837787 | ||||||
| chr16:89837799
|
G | T | 1 | a0001c0001t0001g0108 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.245-7523G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837799 | ||||||
| chr16:89837889
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.245-7433C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837889 | ||||||
| chr16:89837894
|
G | A | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-7428G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837894 | ||||||
| chr16:89837976
|
G | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(194): Show | 197 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.245-7346G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89837976 | ||||||
| chr16:89838003
|
T | G | 14 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(11): Show | 14 | HG01891.hp2 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.245-7319T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838003 | ||||||
| chr16:89838004
|
CTTTT | C | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-7314_245-7311d others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89838004 | |||||
| chr16:89838015
|
T | C | 15 | a0001c0001t0003g0345a0001c0006t0001g0007a0001c0006t0001g0012others(12): Show | 15 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.245-7307T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838015 | ||||||
| chr16:89838018
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(298): Show | 301 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.245-7304A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838018 | ||||||
| chr16:89838018
|
A | T | 3 | a0001c0001t0001g0119a0001c0001t0001g0353a0015c0023t0001g0055 | 3 | HG01071.hp1 HG02300.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.245-7304A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838018 | ||||||
| chr16:89838094
|
G | A | 2 | a0001c0011t0001g0318a0001c0011t0001g0319 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.245-7228G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838094 | ||||||
| chr16:89838121
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.245-7201T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838121 | ||||||
| chr16:89838164
|
A | AT | 8 | a0001c0001t0001g0003a0001c0001t0001g0056a0001c0001t0001g0059others(5): Show | 8 | HG00140.hp1 HG00733.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-7134dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89838164 | |||||
| chr16:89838164
|
AT | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(220): Show | 223 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.245-7134delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89838164 | |||||
| chr16:89838164
|
ATT | A | 46 | a0001c0001t0001g0113a0001c0001t0001g0119a0001c0001t0001g0126others(43): Show | 46 | HG00323.hp2 HG00733.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.245-7135_245-7134d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89838164 | |||||
| chr16:89838164
|
ATTT | A | 11 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0003g0325others(8): Show | 11 | HG02258.hp1 HG02280.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.245-7136_245-7134d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89838164 | |||||
| chr16:89838271
|
C | G | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 13 | HG01891.hp2 HG02451.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.245-7051C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838271 | ||||||
| chr16:89838426
|
G | C | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-6896G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838426 | ||||||
| chr16:89838553
|
G | A | 1 | a0004c0004t0001g0271 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.245-6769G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838553 | ||||||
| chr16:89838563
|
G | A | 10 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(7): Show | 10 | HG00099.hp1 HG00735.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-6759G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838563 | ||||||
| chr16:89838707
|
C | G | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-6615C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838707 | ||||||
| chr16:89838787
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245-6535G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838787 | ||||||
| chr16:89838855
|
G | A | 1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.245-6467G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838855 | ||||||
| chr16:89838928
|
C | T | 5 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(2): Show | 5 | HG02451.hp2 HG02738.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-6394C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89838928 | ||||||
| chr16:89839020
|
T | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.245-6302T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839020 | ||||||
| chr16:89839079
|
C | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0267 | 2 | NA18982.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.245-6243C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839079 | ||||||
| chr16:89839113
|
G | A | 14 | a0001c0006t0001g0007a0001c0006t0001g0012a0001c0006t0001g0013others(11): Show | 14 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.245-6209G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839113 | ||||||
| chr16:89839121
|
C | T | 316 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(313): Show | 316 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.245-6201C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839121 | ||||||
| chr16:89839253
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245-6069A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839253 | ||||||
| chr16:89839373
|
C | CA | 284 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.245-5933dupA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89839373 | |||||
| chr16:89839373
|
C | CAA | 38 | a0001c0001t0001g0002a0001c0001t0001g0099a0001c0001t0001g0116others(35): Show | 38 | HG00438.hp1 HG00609.hp1 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.245-5934_245-5933d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89839373 | |||||
| chr16:89839440
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 233 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.245-5882T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839440 | ||||||
| chr16:89839449
|
T | A | 14 | a0001c0006t0001g0007a0001c0006t0001g0012a0001c0006t0001g0013others(11): Show | 14 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.245-5873T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839449 | ||||||
| chr16:89839451
|
G | A | 2 | a0006c0010t0001g0314a0006c0010t0008g0313 | 2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.245-5871G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839451 | ||||||
| chr16:89839460
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.245-5862C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839460 | ||||||
| chr16:89839472
|
G | C | 8 | a0001c0001t0001g0056a0001c0001t0001g0064a0001c0001t0001g0066others(5): Show | 8 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-5850G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839472 | ||||||
| chr16:89839480
|
C | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0164 | 3 | HG01884.hp2 HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.245-5842C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839480 | ||||||
| chr16:89839517
|
G | C | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 317 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.245-5805G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839517 | ||||||
| chr16:89839518
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.245-5804G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839518 | ||||||
| chr16:89839619
|
C | T | 23 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0337others(20): Show | 23 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.245-5703C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839619 | ||||||
| chr16:89839647
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.245-5675C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839647 | ||||||
| chr16:89839654
|
C | T | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-5668C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839654 | ||||||
| chr16:89839691
|
T | A | 1 | a0001c0003t0001g0101 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.245-5631T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839691 | ||||||
| chr16:89839762
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.245-5560G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839762 | ||||||
| chr16:89839766
|
C | T | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.245-5556C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839766 | ||||||
| chr16:89839795
|
C | G | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-5527C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839795 | ||||||
| chr16:89839912
|
CTG | C | 34 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(31): Show | 34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.245-5402_245-5401d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89839912 | |||||
| chr16:89839956
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.245-5366G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89839956 | ||||||
| chr16:89840001
|
T | A | 1 | a0001c0003t0013g0128 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.245-5321T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840001 | ||||||
| chr16:89840053
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.245-5269T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840053 | ||||||
| chr16:89840092
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0215 | 2 | NA18951.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.245-5230G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840092 | ||||||
| chr16:89840096
|
C | A | 1 | a0002c0002t0002g0024 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.245-5226C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840096 | ||||||
| chr16:89840155
|
G | A | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-5167G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840155 | ||||||
| chr16:89840159
|
G | C | 1 | a0001c0001t0003g0336 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.245-5163G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840159 | ||||||
| chr16:89840245
|
C | CT | 35 | a0001c0001t0001g0002a0001c0001t0001g0084a0001c0001t0001g0085others(32): Show | 35 | HG01106.hp1 HG01106.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.245-5055dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89840245 | |||||
| chr16:89840280
|
C | T | 9 | a0001c0001t0001g0288a0001c0001t0001g0290a0001c0001t0001g0292others(6): Show | 9 | HG00099.hp1 HG00735.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.245-5042C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840280 | ||||||
| chr16:89840312
|
C | T | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.245-5010C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840312 | ||||||
| chr16:89840319
|
G | A | 12 | a0001c0006t0001g0007a0001c0006t0001g0012a0001c0006t0001g0013others(9): Show | 12 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.245-5003G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840319 | ||||||
| chr16:89840392
|
G | A | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-4930G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840392 | ||||||
| chr16:89840399
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.245-4923G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840399 | ||||||
| chr16:89840425
|
ATTTTTAG others(381): Show |
A | 1 | a0001c0001t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.245-4854_245-4467d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89840425 | |||||
| chr16:89840433
|
T | C | 1 | a0001c0001t0007g0026 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.245-4889T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840433 | ||||||
| chr16:89840439
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.245-4883C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840439 | ||||||
| chr16:89840456
|
A | G | 3 | a0001c0001t0001g0150a0001c0001t0001g0321a0001c0001t0001g0322 | 3 | HG02965.hp1 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.245-4866A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840456 | ||||||
| chr16:89840468
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0134others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-4854T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840468 | ||||||
| chr16:89840484
|
T | C | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-4838T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840484 | ||||||
| chr16:89840486
|
G | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0056others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.245-4836G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840486 | ||||||
| chr16:89840490
|
C | T | 1 | a0001c0001t0003g0343 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.245-4832C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840490 | ||||||
| chr16:89840523
|
C | T | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.245-4799C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840523 | ||||||
| chr16:89840528
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-4794A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840528 | ||||||
| chr16:89840529
|
T | A | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-4793T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840529 | ||||||
| chr16:89840594
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.245-4728C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840594 | ||||||
| chr16:89840599
|
G | T | 1 | a0001c0001t0001g0209 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.245-4723G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840599 | ||||||
| chr16:89840636
|
AT | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.245-4667delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89840636 | |||||
| chr16:89840636
|
ATT | A | 10 | a0001c0001t0001g0124a0001c0001t0001g0159a0001c0001t0001g0190others(7): Show | 10 | HG01167.hp1 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-4668_245-4667d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89840636 | |||||
| chr16:89840638
|
T | A | 1 | a0001c0008t0001g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.245-4684T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840638 | ||||||
| chr16:89840646
|
T | G | 1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.245-4676T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840646 | ||||||
| chr16:89840660
|
T | C | 1 | a0008c0013t0002g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.245-4662T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840660 | ||||||
| chr16:89840674
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-4648C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840674 | ||||||
| chr16:89840721
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.245-4601C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840721 | ||||||
| chr16:89840756
|
C | T | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-4566C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840756 | ||||||
| chr16:89840785
|
G | A | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-4537G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840785 | ||||||
| chr16:89840797
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.245-4525A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840797 | ||||||
| chr16:89840839
|
G | A | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-4483G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840839 | ||||||
| chr16:89840935
|
C | G | 1 | a0001c0001t0001g0083 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.245-4387C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89840935 | ||||||
| chr16:89841048
|
G | C | 1 | a0001c0008t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.245-4274G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841048 | ||||||
| chr16:89841085
|
G | T | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-4237G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841085 | ||||||
| chr16:89841112
|
A | T | 1 | a0001c0027t0001g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.245-4210A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841112 | ||||||
| chr16:89841118
|
T | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(269): Show | 272 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.245-4204T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841118 | ||||||
| chr16:89841120
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.245-4202G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841120 | ||||||
| chr16:89841183
|
C | CA | 9 | a0001c0001t0001g0090a0001c0001t0001g0136a0001c0001t0001g0219others(6): Show | 9 | HG01175.hp2 HG01891.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.245-4124dupA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89841183 | |||||
| chr16:89841273
|
C | G | 3 | a0001c0001t0001g0063a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG03942.hp1 HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.245-4049C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841273 | ||||||
| chr16:89841408
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG02717.hp2 HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.245-3914A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841408 | ||||||
| chr16:89841481
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.245-3841C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841481 | ||||||
| chr16:89841539
|
G | A | 30 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.245-3783G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841539 | ||||||
| chr16:89841595
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(204): Show | 207 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.245-3727G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841595 | ||||||
| chr16:89841677
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.245-3645C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841677 | ||||||
| chr16:89841701
|
A | AT | 16 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0001t0001g0071others(13): Show | 16 | HG00099.hp2 HG00733.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.245-3608dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89841701 | |||||
| chr16:89841842
|
C | T | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.245-3480C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89841842 | ||||||
| chr16:89842026
|
C | G | 1 | a0001c0001t0001g0206 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.245-3296C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842026 | ||||||
| chr16:89842145
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.245-3177C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842145 | ||||||
| chr16:89842182
|
A | C | 4 | a0001c0003t0001g0127a0001c0003t0001g0132a0001c0003t0001g0133others(1): Show | 4 | HG01928.hp2 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-3140A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842182 | ||||||
| chr16:89842205
|
G | T | 1 | a0001c0001t0001g0322 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.245-3117G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842205 | ||||||
| chr16:89842208
|
A | AT | 38 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(35): Show | 38 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.245-3092dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | |||||
| chr16:89842208
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-3101_245-3092d others(12): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | |||||
| chr16:89842208
|
A | ATTTTTTT others(5): Show |
15 | a0001c0001t0001g0054a0001c0001t0001g0106a0001c0001t0001g0108others(12): Show | 15 | HG00673.hp1 HG01192.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.245-3103_245-3092d others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | |||||
| chr16:89842208
|
A | ATTTTTTT others(6): Show |
29 | a0001c0001t0001g0091a0001c0001t0001g0104a0001c0001t0001g0107others(26): Show | 29 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.245-3104_245-3092d others(15): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | |||||
| chr16:89842208
|
A | ATTTTTTT others(7): Show |
48 | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0111others(45): Show | 48 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.245-3105_245-3092d others(16): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | |||||
| chr16:89842208
|
A | ATTTTTTT others(8): Show |
65 | a0001c0001t0001g0006a0001c0001t0001g0057a0001c0001t0001g0068others(62): Show | 65 | HG00438.hp1 HG00609.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.245-3106_245-3092d others(17): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | |||||
| chr16:89842208
|
A | ATTTTTTT others(9): Show |
41 | a0001c0001t0001g0002a0001c0001t0001g0087a0001c0001t0001g0099others(38): Show | 41 | HG00408.hp1 HG00673.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.245-3107_245-3092d others(18): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | |||||
| chr16:89842208
|
A | ATTTTTTT others(10): Show |
4 | a0001c0001t0004g0208a0001c0003t0001g0127a0001c0003t0001g0133others(1): Show | 4 | HG01928.hp2 HG01952.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-3108_245-3092d others(19): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | |||||
| chr16:89842208
|
A | ATTTTTTT others(11): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0131 | 2 | HG03579.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.245-3109_245-3092d others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | |||||
| chr16:89842208
|
A | ATTTTTTT others(12): Show |
2 | a0001c0001t0001g0237a0001c0001t0004g0212 | 2 | HG01993.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.245-3110_245-3092d others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | |||||
| chr16:89842208
|
AT | A | 10 | a0001c0001t0001g0354a0001c0006t0001g0007a0001c0006t0001g0012others(7): Show | 10 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.245-3092delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842208 | |||||
| chr16:89842229
|
T | TTTTTTTT others(2): Show |
18 | a0001c0001t0001g0328a0001c0001t0003g0320a0001c0001t0003g0323others(15): Show | 18 | HG01192.hp2 HG02145.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.245-3092_245-3091i others(11): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89842229 | |||||
| chr16:89842236
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(229): Show | 232 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.245-3086G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842236 | ||||||
| chr16:89842258
|
G | C | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-3064G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842258 | ||||||
| chr16:89842598
|
A | G | 2 | a0004c0004t0001g0187a0004c0004t0001g0205 | 2 | NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.245-2724A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842598 | ||||||
| chr16:89842615
|
T | C | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-2707T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842615 | ||||||
| chr16:89842631
|
TGTGGG | T | 4 | a0001c0008t0001g0008a0001c0008t0001g0009a0001c0008t0001g0010others(1): Show | 4 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-2690_245-2686d others(7): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842631 | ||||||
| chr16:89842636
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG02559.hp2 HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.245-2686G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842636 | ||||||
| chr16:89842780
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.245-2542G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842780 | ||||||
| chr16:89842845
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-2477C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842845 | ||||||
| chr16:89842875
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.245-2447G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842875 | ||||||
| chr16:89842963
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2359T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842963 | ||||||
| chr16:89842993
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.245-2329T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89842993 | ||||||
| chr16:89843021
|
A | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0168a0001c0001t0001g0171others(45): Show | 48 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.245-2301A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843021 | ||||||
| chr16:89843068
|
C | T | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-2254C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843068 | ||||||
| chr16:89843111
|
G | A | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-2211G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843111 | ||||||
| chr16:89843238
|
C | A | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.245-2084C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843238 | ||||||
| chr16:89843261
|
T | C | 9 | a0001c0006t0001g0007a0001c0006t0001g0012a0001c0006t0001g0013others(6): Show | 9 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.245-2061T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843261 | ||||||
| chr16:89843294
|
ACGGGAAG others(5): Show |
A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2026_245-2015d others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843294 | |||||
| chr16:89843302
|
T | C | 1 | a0004c0004t0001g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.245-2020T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843302 | ||||||
| chr16:89843308
|
A | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2014A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843308 | ||||||
| chr16:89843311
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2011C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843311 | ||||||
| chr16:89843314
|
C | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2008C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843314 | ||||||
| chr16:89843317
|
C | G | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2005C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843317 | ||||||
| chr16:89843318
|
A | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2004A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843318 | ||||||
| chr16:89843320
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-2002C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843320 | ||||||
| chr16:89843329
|
C | T | 32 | a0001c0019t0001g0317a0002c0002t0002g0022a0002c0002t0002g0023others(29): Show | 32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.245-1993C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843329 | ||||||
| chr16:89843419
|
C | T | 2 | a0001c0001t0004g0204a0001c0001t0004g0212 | 2 | NA18995.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.245-1903C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843419 | ||||||
| chr16:89843533
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.245-1789G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843533 | ||||||
| chr16:89843644
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.245-1678T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843644 | ||||||
| chr16:89843660
|
C | A | 32 | a0001c0019t0001g0317a0002c0002t0002g0022a0002c0002t0002g0023others(29): Show | 32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.245-1662C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843660 | ||||||
| chr16:89843669
|
T | TTTTTTTT others(4): Show |
1 | a0001c0001t0001g0189 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.245-1644_245-1643i others(13): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843669 | |||||
| chr16:89843673
|
TTTTTTTT others(5): Show |
T | 6 | a0001c0006t0001g0012a0001c0006t0001g0014a0001c0006t0001g0016others(3): Show | 6 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-1643_245-1632d others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843673 | |||||
| chr16:89843674
|
TTTTTTTG others(4): Show |
T | 1 | a0001c0001t0003g0333 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.245-1642_245-1632d others(13): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843674 | |||||
| chr16:89843675
|
TTTTTTG | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.245-1643_245-1638d others(8): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843675 | |||||
| chr16:89843676
|
TTTTTG | T | 20 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(17): Show | 20 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.245-1642_245-1638d others(7): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843676 | |||||
| chr16:89843677
|
T | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 4 | HG01978.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-1645T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843677 | ||||||
| chr16:89843677
|
TTTTG | T | 15 | a0002c0002t0002g0024a0002c0002t0002g0028a0002c0002t0002g0030others(12): Show | 15 | HG00609.hp1 HG00621.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.245-1637_245-1634d others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843677 | |||||
| chr16:89843678
|
TTTG | T | 7 | a0002c0002t0002g0022a0002c0002t0002g0027a0002c0002t0002g0038others(4): Show | 7 | HG00438.hp2 HG00597.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-1641_245-1639d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843678 | |||||
| chr16:89843679
|
T | G | 3 | a0001c0006t0001g0007a0001c0006t0001g0013a0001c0009t0001g0019 | 3 | HG04115.hp1 NA18939.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.245-1643T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843679 | ||||||
| chr16:89843680
|
T | G | 1 | a0001c0001t0001g0307 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.245-1642T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843680 | ||||||
| chr16:89843680
|
TGTTTG | T | 4 | a0002c0002t0002g0025a0002c0002t0002g0035a0002c0002t0002g0053others(1): Show | 4 | HG02165.hp1 HG03491.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-1641_245-1637d others(7): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843680 | ||||||
| chr16:89843680
|
TGTTTGTT others(4): Show |
T | 1 | a0001c0009t0001g0019 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.245-1641_245-1631d others(13): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843680 | ||||||
| chr16:89843681
|
G | T | 6 | a0001c0001t0001g0189a0001c0006t0001g0007a0001c0019t0001g0317others(3): Show | 6 | HG02080.hp1 HG03139.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-1641G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843681 | ||||||
| chr16:89843682
|
T | G | 2 | a0001c0001t0001g0100a0001c0003t0001g0127 | 2 | HG01928.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.245-1640T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843682 | ||||||
| chr16:89843685
|
G | T | 30 | a0001c0006t0001g0007a0001c0006t0001g0013a0001c0019t0001g0317others(27): Show | 30 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.245-1637G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843685 | ||||||
| chr16:89843686
|
T | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(230): Show | 233 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.245-1636T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843686 | ||||||
| chr16:89843687
|
TTTTG | T | 11 | a0001c0001t0001g0071a0001c0001t0001g0129a0001c0001t0001g0160others(8): Show | 11 | HG00099.hp2 HG01167.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.245-1631_245-1628d others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843687 | |||||
| chr16:89843688
|
TTTG | T | 164 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0068others(161): Show | 164 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.245-1631_245-1629d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843688 | |||||
| chr16:89843689
|
TTG | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.245-1631_245-1630d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843689 | |||||
| chr16:89843690
|
T | TTTTTTTT others(281): Show |
1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-1632_245-1631i others(290): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843690 | ||||||
| chr16:89843690
|
T | TTTTTTTT others(283): Show |
1 | a0001c0006t0001g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.245-1632_245-1631i others(292): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843690 | ||||||
| chr16:89843690
|
TG | T | 4 | a0001c0001t0001g0175a0001c0003t0001g0101a0001c0003t0001g0278others(1): Show | 4 | HG02080.hp2 HG02647.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-1631delG | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843690 | ||||||
| chr16:89843691
|
G | C | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-1631G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843691 | ||||||
| chr16:89843691
|
G | T | 34 | a0001c0001t0001g0100a0001c0003t0001g0127a0002c0002t0002g0022others(31): Show | 34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.245-1631G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843691 | ||||||
| chr16:89843692
|
T | C | 1 | a0001c0006t0001g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.245-1630T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843692 | ||||||
| chr16:89843692
|
T | TTTTTTTT others(285): Show |
1 | a0001c0006t0001g0013 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.245-1625_245-1624i others(294): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843692 | |||||
| chr16:89843693
|
T | TGAGACAG others(272): Show |
1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.245-1629_245-1628i others(281): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843693 | ||||||
| chr16:89843697
|
TG | T | 4 | a0001c0006t0001g0012a0001c0006t0001g0014a0001c0006t0001g0016others(1): Show | 4 | HG03239.hp2 HG03831.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-1624delG | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843697 | ||||||
| chr16:89843698
|
G | GAGACAGA others(279): Show |
1 | a0001c0001t0001g0189 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.245-1624_245-1623i others(288): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843698 | ||||||
| chr16:89843698
|
G | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.245-1624G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843698 | ||||||
| chr16:89843698
|
GTTT | G | 20 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(17): Show | 20 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.245-1607_245-1605d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843698 | |||||
| chr16:89843701
|
T | G | 1 | a0001c0001t0003g0343 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.245-1621T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843701 | ||||||
| chr16:89843705
|
T | G | 1 | a0001c0001t0001g0215 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.245-1617T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843705 | ||||||
| chr16:89843724
|
GA | G | 5 | a0001c0001t0001g0189a0001c0006t0001g0007a0001c0006t0001g0013others(2): Show | 5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1597delA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843724 | ||||||
| chr16:89843732
|
C | T | 5 | a0001c0001t0001g0189a0001c0006t0001g0007a0001c0006t0001g0013others(2): Show | 5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1590C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843732 | ||||||
| chr16:89843734
|
T | C | 2 | a0001c0001t0001g0189a0001c0019t0001g0317 | 2 | HG03139.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.245-1588T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843734 | ||||||
| chr16:89843742
|
C | A | 5 | a0001c0001t0001g0189a0001c0006t0001g0007a0001c0006t0001g0013others(2): Show | 5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1580C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843742 | ||||||
| chr16:89843750
|
A | C | 5 | a0001c0001t0001g0189a0001c0006t0001g0007a0001c0006t0001g0013others(2): Show | 5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1572A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843750 | ||||||
| chr16:89843752
|
T | C | 5 | a0001c0001t0001g0189a0001c0006t0001g0007a0001c0006t0001g0013others(2): Show | 5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1570T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843752 | ||||||
| chr16:89843758
|
G | T | 5 | a0001c0001t0001g0189a0001c0006t0001g0007a0001c0006t0001g0013others(2): Show | 5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1564G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843758 | ||||||
| chr16:89843760
|
C | CATGATCT others(296): Show |
1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.245-1562_245-1561i others(305): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843760 | ||||||
| chr16:89843760
|
C | CGTGATCT others(612): Show |
1 | a0001c0001t0001g0063 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(621): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(298): Show |
1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(307): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(289): Show |
1 | a0001c0001t0001g0354 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.245-1555_245-1554i others(298): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(297): Show |
22 | a0001c0001t0001g0108a0001c0001t0001g0124a0001c0001t0001g0129others(19): Show | 22 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(306): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(298): Show |
177 | a0001c0001t0001g0006a0001c0001t0001g0054a0001c0001t0001g0057others(174): Show | 177 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(307): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(299): Show |
32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0099others(29): Show | 32 | HG00323.hp2 HG00733.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(308): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(300): Show |
2 | a0001c0001t0001g0353a0001c0012t0005g0272 | 2 | HG02300.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(309): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(301): Show |
1 | a0010c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.245-1555_245-1554i others(310): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(294): Show |
2 | a0001c0001t0001g0328a0001c0001t0003g0329 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(303): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(295): Show |
11 | a0001c0001t0001g0071a0001c0001t0003g0325a0001c0001t0003g0326others(8): Show | 11 | HG00099.hp2 HG01192.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(304): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(295): Show |
1 | a0001c0006t0001g0012 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(304): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(296): Show |
34 | a0001c0001t0003g0320a0001c0001t0003g0332a0001c0001t0003g0334others(31): Show | 34 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(305): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(296): Show |
6 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0009t0001g0017others(3): Show | 6 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(305): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(297): Show |
5 | a0001c0001t0003g0323a0002c0002t0002g0045a0002c0002t0002g0047others(2): Show | 5 | HG00438.hp2 HG02040.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(306): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(298): Show |
1 | a0001c0001t0003g0344 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.245-1555_245-1554i others(307): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(639): Show |
1 | a0001c0001t0001g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(648): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(638): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0282 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(647): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(635): Show |
2 | a0001c0001t0001g0279a0001c0001t0001g0284 | 2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(644): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(636): Show |
2 | a0001c0001t0001g0280a0001c0001t0001g0285 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(645): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(634): Show |
2 | a0001c0001t0001g0281a0001c0001t0001g0286 | 2 | HG02886.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(643): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(635): Show |
1 | a0001c0001t0001g0283 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(644): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(632): Show |
1 | a0001c0001t0001g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(641): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(630): Show |
1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(639): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(629): Show |
1 | a0001c0008t0001g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(638): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(628): Show |
1 | a0001c0001t0001g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.245-1555_245-1554i others(637): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(626): Show |
4 | a0001c0008t0001g0008a0001c0008t0001g0011a0001c0011t0001g0318others(1): Show | 4 | HG01167.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(635): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(639): Show |
1 | a0001c0001t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(648): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(616): Show |
1 | a0001c0008t0001g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.245-1555_245-1554i others(625): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(613): Show |
1 | a0001c0001t0001g0059 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.245-1555_245-1554i others(622): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(611): Show |
2 | a0001c0001t0001g0069a0001c0001t0001g0086 | 2 | HG00140.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.245-1555_245-1554i others(620): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(612): Show |
20 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0061others(17): Show | 20 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(621): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(613): Show |
4 | a0001c0001t0001g0060a0001c0001t0001g0082a0001c0001t0001g0089others(1): Show | 4 | HG00741.hp2 HG01175.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(622): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | CGTGATCT others(612): Show |
5 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG00642.hp1 HG01074.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1555_245-1554i others(621): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89843760 | |||||
| chr16:89843760
|
C | T | 5 | a0001c0001t0001g0189a0001c0006t0001g0007a0001c0006t0001g0013others(2): Show | 5 | HG03139.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1562C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843760 | ||||||
| chr16:89843818
|
G | A | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.245-1504G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843818 | ||||||
| chr16:89843822
|
C | G | 32 | a0001c0019t0001g0317a0002c0002t0002g0022a0002c0002t0002g0023others(29): Show | 32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.245-1500C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843822 | ||||||
| chr16:89843842
|
T | G | 36 | a0001c0001t0002g0051a0001c0001t0007g0026a0001c0019t0001g0317others(33): Show | 36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.245-1480T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843842 | ||||||
| chr16:89843948
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0286 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.245-1374G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89843948 | ||||||
| chr16:89844000
|
C | CT | 6 | a0001c0001t0001g0100a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 6 | HG03041.hp2 HG03225.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-1309dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89844000 | |||||
| chr16:89844027
|
ACT | A | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0014c0024t0001g0270 | 3 | HG02071.hp2 HG03927.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.245-1292_245-1291d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 89844027 | |||||
| chr16:89844073
|
G | A | 1 | a0002c0002t0002g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1249G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844073 | ||||||
| chr16:89844080
|
C | A | 1 | a0002c0002t0002g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1242C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844080 | ||||||
| chr16:89844081
|
A | G | 1 | a0002c0002t0002g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1241A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844081 | ||||||
| chr16:89844083
|
C | T | 1 | a0002c0002t0002g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1239C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844083 | ||||||
| chr16:89844085
|
T | G | 1 | a0002c0002t0002g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1237T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844085 | ||||||
| chr16:89844087
|
C | G | 1 | a0002c0002t0002g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1235C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844087 | ||||||
| chr16:89844090
|
G | T | 1 | a0002c0002t0002g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.245-1232G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844090 | ||||||
| chr16:89844128
|
C | T | 1 | a0001c0001t0004g0230 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.245-1194C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844128 | ||||||
| chr16:89844155
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.245-1167T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844155 | ||||||
| chr16:89844280
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.245-1042C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844280 | ||||||
| chr16:89844309
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.245-1013C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844309 | ||||||
| chr16:89844425
|
C | T | 28 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.245-897C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844425 | ||||||
| chr16:89844429
|
G | T | 1 | a0001c0001t0003g0343 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.245-893G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844429 | ||||||
| chr16:89844432
|
T | A | 1 | a0003c0005t0001g0295 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.245-890T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844432 | ||||||
| chr16:89844473
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.245-849C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844473 | ||||||
| chr16:89844532
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.245-790G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844532 | ||||||
| chr16:89844539
|
C | T | 23 | a0001c0001t0001g0071a0001c0001t0001g0328a0001c0001t0001g0337others(20): Show | 23 | HG00099.hp2 HG01109.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.245-783C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844539 | ||||||
| chr16:89844692
|
C | T | 1 | a0001c0003t0001g0120 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.245-630C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844692 | ||||||
| chr16:89844718
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.245-604G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844718 | ||||||
| chr16:89844764
|
G | T | 3 | a0001c0008t0001g0008a0001c0008t0001g0010a0001c0008t0001g0011 | 3 | HG01167.hp2 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.245-558G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844764 | ||||||
| chr16:89844832
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.245-490C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844832 | ||||||
| chr16:89844840
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.245-482C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89844840 | ||||||
| chr16:89845103
|
G | A | 3 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286 | 3 | HG02257.hp2 HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.245-219G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89845103 | ||||||
| chr16:89845217
|
A | G | 1 | a0001c0003t0001g0102 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.245-105A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89845217 | ||||||
| chr16:89845220
|
G | T | 1 | a0007c0026t0001g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.245-102G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89845220 | ||||||
| chr16:89845273
|
G | C | 28 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.245-49G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 1/14 | chr16 | 89845273 | ||||||
| chr16:89845446
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.288+81T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845446 | ||||||
| chr16:89845592
|
C | T | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.288+227C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845592 | ||||||
| chr16:89845640
|
G | A | 13 | a0001c0001t0001g0302a0001c0001t0001g0303a0003c0005t0001g0296others(10): Show | 13 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.288+275G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845640 | ||||||
| chr16:89845655
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(230): Show | 233 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.288+290T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845655 | ||||||
| chr16:89845873
|
G | C | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.288+508G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845873 | ||||||
| chr16:89845918
|
A | G | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.288+553A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845918 | ||||||
| chr16:89845991
|
G | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(204): Show | 207 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.288+626G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89845991 | ||||||
| chr16:89846047
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.288+682C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846047 | ||||||
| chr16:89846049
|
A | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(227): Show | 230 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.288+684A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846049 | ||||||
| chr16:89846054
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(224): Show | 227 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.288+689G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846054 | ||||||
| chr16:89846057
|
C | T | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.288+692C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846057 | ||||||
| chr16:89846058
|
G | A | 10 | a0001c0006t0001g0007a0001c0006t0001g0012a0001c0006t0001g0013others(7): Show | 10 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+693G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846058 | ||||||
| chr16:89846099
|
G | A | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.288+734G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846099 | ||||||
| chr16:89846312
|
C | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(234): Show | 237 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.288+947C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846312 | ||||||
| chr16:89846328
|
C | CT | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.288+974dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89846328 | |||||
| chr16:89846416
|
C | T | 2 | a0001c0001t0003g0336a0001c0001t0003g0345 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.288+1051C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846416 | ||||||
| chr16:89846429
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.288+1064G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846429 | ||||||
| chr16:89846499
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.288+1134C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846499 | ||||||
| chr16:89846517
|
GT | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.288+1161delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89846517 | |||||
| chr16:89846600
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0099others(106): Show | 109 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.288+1235G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846600 | ||||||
| chr16:89846756
|
C | T | 41 | a0001c0001t0004g0170a0001c0001t0004g0204a0001c0001t0004g0212others(38): Show | 41 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.288+1391C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846756 | ||||||
| chr16:89846810
|
C | CT | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.288+1462dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89846810 | |||||
| chr16:89846871
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.288+1506C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846871 | ||||||
| chr16:89846880
|
C | T | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.288+1515C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846880 | ||||||
| chr16:89846930
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.288+1565G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846930 | ||||||
| chr16:89846964
|
C | T | 1 | a0001c0003t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.288+1599C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89846964 | ||||||
| chr16:89846973
|
GATTA | G | 10 | a0001c0006t0001g0007a0001c0006t0001g0012a0001c0006t0001g0013others(7): Show | 10 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+1612_288+1615d others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89846973 | |||||
| chr16:89847023
|
C | T | 2 | a0001c0006t0001g0007a0001c0006t0001g0014 | 2 | NA18939.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.288+1658C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847023 | ||||||
| chr16:89847252
|
C | G | 1 | a0001c0001t0001g0184 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.288+1887C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847252 | ||||||
| chr16:89847318
|
G | A | 10 | a0001c0006t0001g0007a0001c0006t0001g0012a0001c0006t0001g0013others(7): Show | 10 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+1953G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847318 | ||||||
| chr16:89847327
|
C | T | 2 | a0001c0001t0001g0321a0001c0001t0001g0322 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.288+1962C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847327 | ||||||
| chr16:89847385
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.288+2020C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847385 | ||||||
| chr16:89847392
|
C | G | 1 | a0001c0008t0001g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.288+2027C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847392 | ||||||
| chr16:89847402
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.288+2037G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847402 | ||||||
| chr16:89847408
|
G | A | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.288+2043G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847408 | ||||||
| chr16:89847466
|
A | T | 10 | a0001c0006t0001g0007a0001c0006t0001g0012a0001c0006t0001g0013others(7): Show | 10 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+2101A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847466 | ||||||
| chr16:89847588
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.288+2223A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847588 | ||||||
| chr16:89847839
|
T | G | 2 | a0001c0001t0001g0337a0001c0001t0003g0330 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.289-2465T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847839 | ||||||
| chr16:89847886
|
C | T | 1 | a0001c0018t0012g0346 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.289-2418C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847886 | ||||||
| chr16:89847943
|
G | A | 2 | a0001c0001t0003g0336a0001c0001t0003g0345 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.289-2361G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89847943 | ||||||
| chr16:89848013
|
G | A | 6 | a0001c0001t0001g0112a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 6 | HG01891.hp1 HG02970.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-2291G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848013 | ||||||
| chr16:89848017
|
C | T | 8 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(5): Show | 8 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.289-2287C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848017 | ||||||
| chr16:89848059
|
G | A | 1 | a0001c0001t0004g0204 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.289-2245G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848059 | ||||||
| chr16:89848085
|
C | T | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.289-2219C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848085 | ||||||
| chr16:89848100
|
C | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(270): Show | 273 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.289-2204C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848100 | ||||||
| chr16:89848186
|
G | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG02738.hp1 HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.289-2118G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848186 | ||||||
| chr16:89848225
|
T | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.289-2079T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848225 | ||||||
| chr16:89848397
|
A | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.289-1907A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848397 | ||||||
| chr16:89848438
|
TGGCGTTT others(37): Show |
T | 3 | a0001c0001t0001g0064a0001c0011t0001g0318a0001c0011t0001g0319 | 3 | HG01081.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.289-1822_289-1779d others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848438 | |||||
| chr16:89848486
|
GTTTCTGC others(81): Show |
G | 31 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(28): Show | 31 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.289-1778_289-1691d others(90): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848486 | |||||
| chr16:89848526
|
T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.289-1778T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848526 | ||||||
| chr16:89848545
|
A | T | 1 | a0001c0003t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.289-1759A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848545 | ||||||
| chr16:89848571
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.289-1733A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848571 | ||||||
| chr16:89848634
|
T | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | NA18949.hp1 NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.289-1670T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848634 | ||||||
| chr16:89848659
|
G | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.289-1645G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848659 | ||||||
| chr16:89848738
|
GCCTTCTG others(37): Show |
G | 1 | a0001c0001t0001g0086 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.289-1522_289-1479d others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848738 | |||||
| chr16:89848781
|
G | T | 1 | a0001c0001t0001g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.289-1523G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848781 | ||||||
| chr16:89848822
|
C | T | 1 | a0004c0004t0001g0205 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.289-1482C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848822 | ||||||
| chr16:89848835
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0221 | 2 | HG02735.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.289-1469G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848835 | ||||||
| chr16:89848878
|
CGGCGTTT others(125): Show |
C | 32 | a0001c0019t0001g0317a0002c0002t0002g0022a0002c0002t0002g0023others(29): Show | 32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.289-1406_289-1275d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848878 | |||||
| chr16:89848906
|
G | GTTCCAGG others(301): Show |
1 | a0003c0005t0001g0295 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.289-1380_289-1379i others(310): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848906 | |||||
| chr16:89848906
|
G | GTTCCAGG others(301): Show |
1 | a0003c0005t0001g0311 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.289-1363_289-1362i others(310): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848906 | |||||
| chr16:89848906
|
G | GTTCCAGG others(37): Show |
27 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.289-1363_289-1362i others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89848906 | |||||
| chr16:89848942
|
C | T | 2 | a0004c0004t0001g0355a0004c0004t0001g0356 | 2 | NA18945.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.289-1362C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848942 | ||||||
| chr16:89848947
|
C | G | 1 | a0001c0001t0001g0160 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289-1357C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89848947 | ||||||
| chr16:89849010
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.289-1294T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849010 | ||||||
| chr16:89849088
|
G | A | 1 | a0004c0004t0001g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.289-1216G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849088 | ||||||
| chr16:89849158
|
A | G | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.289-1146A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849158 | ||||||
| chr16:89849408
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.289-896G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849408 | ||||||
| chr16:89849424
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.289-880G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849424 | ||||||
| chr16:89849429
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.289-875A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849429 | ||||||
| chr16:89849786
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.289-518G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849786 | ||||||
| chr16:89849828
|
G | A | 29 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.289-476G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849828 | ||||||
| chr16:89849844
|
C | CT | 36 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(33): Show | 36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.289-449dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89849844 | |||||
| chr16:89849844
|
CT | C | 7 | a0001c0001t0001g0062a0001c0001t0001g0081a0001c0001t0001g0082others(4): Show | 7 | HG00741.hp2 HG01256.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.289-449delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 89849844 | |||||
| chr16:89849873
|
TG | T | 6 | a0001c0001t0001g0172a0001c0001t0001g0216a0001c0001t0001g0228others(3): Show | 6 | HG01993.hp2 HG02148.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-430delG | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849873 | ||||||
| chr16:89849983
|
G | A | 137 | a0001c0001t0001g0054a0001c0001t0001g0071a0001c0001t0001g0091others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.289-321G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89849983 | ||||||
| chr16:89850192
|
C | A | 32 | a0001c0019t0001g0317a0002c0002t0002g0022a0002c0002t0002g0023others(29): Show | 32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.289-112C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89850192 | ||||||
| chr16:89850276
|
G | A | 2 | a0002c0002t0002g0025a0002c0002t0002g0050 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.289-28G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89850276 | ||||||
| chr16:89850300
|
G | A | 1 | a0001c0001t0003g0334 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.289-4G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 2/14 | chr16 | 89850300 | ||||||
| chr16:89850722
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.645+62G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850722 | ||||||
| chr16:89850749
|
C | T | 1 | a0001c0008t0001g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.645+89C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850749 | ||||||
| chr16:89850824
|
G | GTT | 28 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(25): Show | 28 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.645+165_645+166dup others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89850824 | |||||
| chr16:89850824
|
G | GTTT | 3 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0037 | 3 | HG02083.hp1 NA18967.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.645+166_645+167ins others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89850824 | |||||
| chr16:89850827
|
G | T | 59 | a0001c0001t0001g0071a0001c0001t0001g0328a0001c0001t0001g0337others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.645+167G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850827 | ||||||
| chr16:89850832
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.645+172T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850832 | ||||||
| chr16:89850835
|
G | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0071others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.645+175G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850835 | ||||||
| chr16:89850850
|
T | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(203): Show | 206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.645+190T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850850 | ||||||
| chr16:89850867
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.645+207A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850867 | ||||||
| chr16:89850967
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.645+307G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850967 | ||||||
| chr16:89850988
|
C | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0160a0012c0017t0001g0148 | 3 | HG02145.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.645+328C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850988 | ||||||
| chr16:89850990
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.645+330C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89850990 | ||||||
| chr16:89851021
|
A | T | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.645+361A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851021 | ||||||
| chr16:89851064
|
A | G | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.645+404A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851064 | ||||||
| chr16:89851072
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.645+412C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851072 | ||||||
| chr16:89851098
|
G | A | 1 | a0001c0001t0001g0327 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.645+438G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851098 | ||||||
| chr16:89851129
|
T | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.645+469T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851129 | ||||||
| chr16:89851215
|
G | A | 1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.645+555G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851215 | ||||||
| chr16:89851322
|
A | G | 1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.645+662A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851322 | ||||||
| chr16:89851340
|
C | T | 26 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(23): Show | 26 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.645+680C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851340 | ||||||
| chr16:89851367
|
C | T | 32 | a0001c0019t0001g0317a0002c0002t0002g0022a0002c0002t0002g0023others(29): Show | 32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.645+707C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851367 | ||||||
| chr16:89851396
|
C | T | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+736C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851396 | ||||||
| chr16:89851470
|
G | A | 1 | a0001c0001t0004g0204 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.645+810G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851470 | ||||||
| chr16:89851519
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.645+859C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851519 | ||||||
| chr16:89851557
|
G | A | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.645+897G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851557 | ||||||
| chr16:89851764
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.645+1104C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851764 | ||||||
| chr16:89851949
|
C | G | 9 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0137others(6): Show | 9 | HG02451.hp1 HG02976.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.645+1289C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89851949 | ||||||
| chr16:89852013
|
T | TCTCCCCC others(32): Show |
6 | a0001c0001t0001g0087a0001c0001t0001g0100a0001c0001t0001g0107others(3): Show | 6 | HG00597.hp1 HG00733.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.645+1361_645+1399d others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852013 | |||||
| chr16:89852015
|
T | TC | 7 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0180others(4): Show | 7 | HG01106.hp2 HG01175.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.645+1361dupC | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852015 | |||||
| chr16:89852026
|
CCCAGATC others(32): Show |
C | 1 | a0001c0001t0001g0266 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.645+1400_645+1438d others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852026 | |||||
| chr16:89852036
|
CTGGCCCA others(71): Show |
C | 1 | a0001c0003t0001g0278 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.645+1400_645+1477d others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852036 | |||||
| chr16:89852036
|
CTGGCCCA others(149): Show |
C | 1 | a0001c0001t0001g0126 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.645+1400_645+1555d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852036 | |||||
| chr16:89852037
|
TGGCCCAT others(31): Show |
T | 1 | a0001c0006t0001g0012 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.645+1378_645+1415d others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852037 | ||||||
| chr16:89852060
|
A | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0054others(189): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.645+1400A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852060 | ||||||
| chr16:89852060
|
A | G | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1400A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852060 | ||||||
| chr16:89852061
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.645+1401A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852061 | ||||||
| chr16:89852065
|
G | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0054others(191): Show | 194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.645+1405G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852065 | ||||||
| chr16:89852069
|
G | T | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1409G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852069 | ||||||
| chr16:89852072
|
C | T | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1412C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852072 | ||||||
| chr16:89852075
|
C | A | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1415C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852075 | ||||||
| chr16:89852075
|
C | CTGGCCCA others(149): Show |
1 | a0001c0001t0001g0234 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.645+1443_645+1444i others(158): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852075 | |||||
| chr16:89852075
|
CTGGCCCA others(32): Show |
C | 1 | a0001c0001t0001g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.645+1444_645+1482d others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852075 | |||||
| chr16:89852076
|
T | TGGCCCAT others(504): Show |
1 | a0001c0001t0001g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.645+1438_645+1439i others(513): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852076 | |||||
| chr16:89852089
|
A | G | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1429A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852089 | ||||||
| chr16:89852095
|
C | CCCCAACC others(71): Show |
1 | a0001c0001t0001g0057 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.645+1438_645+1439i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852095 | |||||
| chr16:89852095
|
C | T | 1 | a0005c0014t0002g0021 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.645+1435C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852095 | ||||||
| chr16:89852098
|
C | T | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1438C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852098 | ||||||
| chr16:89852099
|
C | A | 80 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0084others(77): Show | 80 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.645+1439C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852099 | ||||||
| chr16:89852102
|
C | A | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1442C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852102 | ||||||
| chr16:89852104
|
A | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0099others(117): Show | 120 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.645+1444A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852104 | ||||||
| chr16:89852104
|
A | G | 70 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0084others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.645+1444A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852104 | ||||||
| chr16:89852107
|
A | G | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1447A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852107 | ||||||
| chr16:89852114
|
A | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0054others(178): Show | 181 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.645+1454A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852114 | ||||||
| chr16:89852115
|
T | TGGCCCAT others(32): Show |
1 | a0001c0008t0001g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.645+1473_645+1474i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852115 | |||||
| chr16:89852121
|
A | G | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1461A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852121 | ||||||
| chr16:89852128
|
A | ATCCTCTC others(1596): Show |
1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.645+1473_645+1474i others(1605): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852128 | |||||
| chr16:89852128
|
A | G | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1468A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852128 | ||||||
| chr16:89852134
|
C | T | 10 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(7): Show | 10 | HG00735.hp2 HG01109.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.645+1474C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852134 | ||||||
| chr16:89852134
|
CCCCCACC others(32): Show |
C | 1 | a0001c0003t0001g0101 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.645+1483_645+1521d others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852134 | |||||
| chr16:89852137
|
C | T | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1477C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852137 | ||||||
| chr16:89852138
|
C | A | 2 | a0001c0001t0001g0160a0012c0017t0001g0148 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.645+1478C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852138 | ||||||
| chr16:89852138
|
C | T | 30 | a0001c0019t0001g0317a0002c0002t0002g0022a0002c0002t0002g0023others(27): Show | 30 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.645+1478C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852138 | ||||||
| chr16:89852143
|
C | A | 84 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0084others(81): Show | 84 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.645+1483C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852143 | ||||||
| chr16:89852143
|
C | CCCAGATC others(71): Show |
1 | a0001c0001t0001g0107 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.645+1512_645+1513i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852143 | |||||
| chr16:89852143
|
C | G | 3 | a0001c0001t0001g0160a0001c0006t0001g0012a0012c0017t0001g0148 | 3 | HG02922.hp2 HG03471.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.645+1483C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852143 | ||||||
| chr16:89852146
|
A | G | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1486A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852146 | ||||||
| chr16:89852150
|
CCCATGGC others(188): Show |
C | 3 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0324 | 3 | HG01192.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.645+1513_645+1707d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852150 | |||||
| chr16:89852153
|
A | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0099others(106): Show | 109 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.645+1493A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852153 | ||||||
| chr16:89852156
|
G | A | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1496G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852156 | ||||||
| chr16:89852157
|
C | T | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1497C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852157 | ||||||
| chr16:89852160
|
A | G | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1500A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852160 | ||||||
| chr16:89852167
|
A | G | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1507A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852167 | ||||||
| chr16:89852167
|
ATCCTCTC others(701): Show |
A | 10 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 10 | HG01891.hp2 HG02451.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.645+1513_646-1406d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852167 | |||||
| chr16:89852172
|
CTCCCCAC others(148): Show |
C | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1513_645+1667d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852172 | ||||||
| chr16:89852173
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0054others(197): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.645+1513T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852173 | ||||||
| chr16:89852177
|
C | A | 1 | a0001c0003t0001g0278 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.645+1517C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852177 | ||||||
| chr16:89852182
|
A | ACCAGATC others(343): Show |
1 | a0001c0001t0001g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.645+1555_645+1556i others(352): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852182 | |||||
| chr16:89852182
|
A | ACCAGATC others(109): Show |
3 | a0001c0008t0001g0008a0001c0008t0001g0010a0001c0008t0001g0011 | 3 | HG01167.hp2 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.645+1563_645+1564i others(118): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852182 | |||||
| chr16:89852182
|
A | C | 92 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0001t0001g0071others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.645+1522A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852182 | ||||||
| chr16:89852182
|
A | G | 1 | a0001c0003t0001g0278 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.645+1522A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852182 | ||||||
| chr16:89852189
|
C | CCCATGGC others(927): Show |
1 | a0001c0001t0001g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.645+1555_645+1556i others(936): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852189 | |||||
| chr16:89852189
|
C | T | 2 | a0001c0001t0001g0071a0005c0014t0002g0021 | 2 | HG00099.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.645+1529C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852189 | ||||||
| chr16:89852189
|
CCCATGGC others(149): Show |
C | 1 | a0003c0005t0001g0300 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.645+1600_645+1755d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852189 | |||||
| chr16:89852192
|
A | ATGGCCCA others(266): Show |
1 | a0001c0008t0001g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.645+1563_645+1564i others(275): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852192 | |||||
| chr16:89852192
|
A | ATGGCCCA others(110): Show |
3 | a0001c0001t0003g0323a0001c0001t0003g0331a0001c0001t0003g0338 | 3 | HG02145.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.645+1551_645+1552i others(119): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852192 | |||||
| chr16:89852192
|
A | C | 25 | a0001c0001t0001g0057a0001c0001t0001g0087a0001c0001t0001g0100others(22): Show | 25 | HG00597.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.645+1532A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852192 | ||||||
| chr16:89852210
|
TC | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0056a0001c0001t0001g0059others(40): Show | 43 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.645+1556delC | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852210 | |||||
| chr16:89852212
|
C | CCCCACCC others(226): Show |
1 | a0001c0001t0001g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.645+1555_645+1556i others(235): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852212 | |||||
| chr16:89852212
|
C | CCCCACCC others(31): Show |
2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.645+1555_645+1556i others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852212 | |||||
| chr16:89852212
|
C | T | 21 | a0001c0001t0001g0054a0001c0001t0001g0134a0001c0001t0001g0328others(18): Show | 21 | HG01109.hp2 HG01192.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.645+1552C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852212 | ||||||
| chr16:89852214
|
C | T | 2 | a0001c0001t0001g0156a0010c0016t0001g0005 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.645+1554C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852214 | ||||||
| chr16:89852216
|
C | A | 2 | a0001c0001t0001g0087a0004c0004t0001g0186 | 2 | HG00733.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.645+1556C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852216 | ||||||
| chr16:89852216
|
C | T | 2 | a0002c0002t0002g0024a0002c0002t0002g0053 | 2 | HG02165.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.645+1556C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852216 | ||||||
| chr16:89852221
|
C | A | 9 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0134others(6): Show | 9 | HG00099.hp2 HG00621.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.645+1561C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852221 | ||||||
| chr16:89852221
|
C | CCCAGATC others(32): Show |
1 | a0001c0001t0001g0057 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.645+1570_645+1571i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852221 | |||||
| chr16:89852221
|
C | G | 2 | a0001c0001t0001g0087a0004c0004t0001g0186 | 2 | HG00733.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.645+1561C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852221 | ||||||
| chr16:89852222
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.645+1562C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852222 | ||||||
| chr16:89852224
|
A | AGATCCCC others(463): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0152a0001c0001t0001g0153others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.645+1570_645+1571i others(472): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852224 | |||||
| chr16:89852224
|
A | G | 3 | a0001c0001t0001g0058a0001c0001t0001g0156a0010c0016t0001g0005 | 3 | HG01884.hp2 HG03688.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.645+1564A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852224 | ||||||
| chr16:89852225
|
G | T | 3 | a0001c0001t0003g0323a0001c0001t0003g0331a0001c0001t0003g0338 | 3 | HG02145.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.645+1565G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852225 | ||||||
| chr16:89852228
|
C | CCCATGGC others(32): Show |
2 | a0002c0002t0002g0023a0002c0002t0002g0031 | 2 | HG00323.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.645+1590_645+1591i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852228 | |||||
| chr16:89852228
|
C | T | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.645+1568C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852228 | ||||||
| chr16:89852231
|
A | ATGGCCCA others(188): Show |
2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.645+1599_645+1600i others(197): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852231 | |||||
| chr16:89852231
|
A | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0057a0001c0001t0001g0068others(115): Show | 118 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.645+1571A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852231 | ||||||
| chr16:89852232
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.645+1572T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852232 | ||||||
| chr16:89852238
|
A | G | 4 | a0001c0001t0001g0134a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02622.hp2 HG03927.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1578A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852238 | ||||||
| chr16:89852245
|
A | G | 1 | a0010c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.645+1585A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852245 | ||||||
| chr16:89852251
|
C | T | 36 | a0001c0001t0001g0083a0001c0001t0001g0134a0001c0001t0001g0135others(33): Show | 36 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.645+1591C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852251 | ||||||
| chr16:89852251
|
CCCCCACC others(32): Show |
C | 1 | a0003c0005t0001g0295 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.645+1630_645+1668d others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852251 | |||||
| chr16:89852251
|
CCCCCACC others(188): Show |
C | 1 | a0001c0001t0001g0191 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.645+1630_646-1802d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852251 | |||||
| chr16:89852253
|
C | T | 30 | a0001c0001t0001g0104a0001c0001t0001g0158a0001c0001t0001g0159others(27): Show | 30 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.645+1593C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852253 | ||||||
| chr16:89852255
|
C | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0068others(31): Show | 34 | HG01071.hp1 HG01106.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.645+1595C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852255 | ||||||
| chr16:89852255
|
C | CACCCCCC others(32): Show |
2 | a0001c0001t0001g0177a0001c0001t0001g0267 | 2 | HG01934.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.645+1599_645+1600i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852255 | |||||
| chr16:89852255
|
C | T | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.645+1595C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852255 | ||||||
| chr16:89852260
|
A | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.645+1600A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852260 | ||||||
| chr16:89852260
|
A | G | 27 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0084others(24): Show | 27 | HG01071.hp1 HG01106.hp1 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.645+1600A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852260 | ||||||
| chr16:89852262
|
C | T | 1 | a0010c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.645+1602C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852262 | ||||||
| chr16:89852263
|
A | AGATCCCA others(149): Show |
1 | a0001c0001t0003g0343 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.645+1629_645+1630i others(158): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852263 | |||||
| chr16:89852263
|
A | G | 36 | a0001c0001t0001g0104a0001c0001t0001g0158a0001c0001t0001g0159others(33): Show | 36 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.645+1603A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852263 | ||||||
| chr16:89852267
|
C | T | 25 | a0001c0001t0001g0210a0001c0019t0001g0317a0002c0002t0002g0022others(22): Show | 25 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.645+1607C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852267 | ||||||
| chr16:89852267
|
CCCATGGC others(71): Show |
C | 9 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0112others(6): Show | 9 | HG01891.hp1 HG03017.hp2 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.645+1630_645+1707d others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852267 | |||||
| chr16:89852270
|
A | ATGGCCCA others(385): Show |
1 | a0001c0001t0001g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.645+1629_645+1630i others(394): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852270 | |||||
| chr16:89852270
|
A | ATGGCCCA others(32): Show |
1 | a0001c0001t0001g0213 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.645+1629_645+1630i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852270 | |||||
| chr16:89852270
|
A | ATGGCCCG others(71): Show |
1 | a0001c0001t0001g0087 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.645+1616_645+1617i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852270 | |||||
| chr16:89852270
|
A | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.645+1610A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852270 | ||||||
| chr16:89852271
|
T | TGGCCCAT others(500): Show |
1 | a0001c0001t0001g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.645+1629_645+1630i others(509): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852271 | |||||
| chr16:89852271
|
T | TGGCCCAT others(306): Show |
1 | a0001c0001t0001g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.645+1629_645+1630i others(315): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852271 | |||||
| chr16:89852277
|
A | ATCTTCCA others(506): Show |
1 | a0001c0001t0001g0354 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.645+1629_645+1630i others(515): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852277 | |||||
| chr16:89852284
|
A | G | 4 | a0001c0001t0001g0350a0004c0004t0001g0173a0004c0004t0001g0194others(1): Show | 4 | HG00408.hp1 HG03669.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+1624A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852284 | ||||||
| chr16:89852289
|
C | CCCCCCAC others(419): Show |
1 | a0001c0001t0001g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.645+1629_645+1630i others(428): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852289 | ||||||
| chr16:89852290
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.645+1630T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852290 | ||||||
| chr16:89852292
|
C | CCCACCCC others(773): Show |
1 | a0001c0009t0001g0019 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.645+1638_645+1639i others(782): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852292 | |||||
| chr16:89852292
|
C | CCCACCCC others(891): Show |
1 | a0001c0009t0001g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.645+1638_645+1639i others(900): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852292 | |||||
| chr16:89852292
|
C | CCCACCCC others(500): Show |
1 | a0001c0009t0001g0017 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.645+1638_645+1639i others(509): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852292 | |||||
| chr16:89852292
|
C | T | 13 | a0001c0001t0001g0134a0001c0001t0001g0248a0001c0001t0001g0249others(10): Show | 13 | HG00099.hp1 HG01109.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.645+1632C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852292 | ||||||
| chr16:89852292
|
CCCACCCA others(305): Show |
C | 1 | a0001c0001t0001g0149 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.645+1639_646-1676d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852292 | |||||
| chr16:89852293
|
C | CCACCCCC others(113): Show |
1 | a0001c0001t0001g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.645+1638_645+1639i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852293 | |||||
| chr16:89852294
|
C | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0087others(84): Show | 87 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.645+1634C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852294 | ||||||
| chr16:89852294
|
C | T | 1 | a0002c0002t0002g0034 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.645+1634C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852294 | ||||||
| chr16:89852299
|
A | ACCAGATC others(1163): Show |
1 | a0001c0011t0001g0319 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.645+1681_645+1682i others(1172): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852299 | |||||
| chr16:89852299
|
A | C | 123 | a0001c0001t0001g0057a0001c0001t0001g0071a0001c0001t0001g0083others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.645+1639A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852299 | ||||||
| chr16:89852299
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0087others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.645+1639A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852299 | ||||||
| chr16:89852299
|
ACCAGATC others(188): Show |
A | 1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.645+1671_646-1761d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852299 | |||||
| chr16:89852301
|
C | T | 8 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0160others(5): Show | 8 | HG00408.hp1 HG02717.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.645+1641C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852301 | ||||||
| chr16:89852302
|
A | AGATCCCA others(112): Show |
3 | a0001c0001t0001g0104a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG02717.hp2 HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.645+1672_645+1673i others(121): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852302 | |||||
| chr16:89852302
|
A | AGATCCCA others(110): Show |
3 | a0001c0001t0003g0323a0001c0001t0003g0331a0001c0001t0003g0338 | 3 | HG02145.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.645+1681_645+1682i others(119): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852302 | |||||
| chr16:89852302
|
A | G | 23 | a0001c0001t0001g0134a0001c0001t0001g0141a0001c0001t0001g0145others(20): Show | 23 | HG00099.hp1 HG00408.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.645+1642A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852302 | ||||||
| chr16:89852303
|
G | T | 1 | a0005c0014t0002g0021 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.645+1643G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852303 | ||||||
| chr16:89852306
|
C | T | 1 | a0005c0014t0002g0021 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.645+1646C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852306 | ||||||
| chr16:89852309
|
A | ATGGCCCA others(149): Show |
2 | a0002c0002t0002g0024a0002c0002t0002g0053 | 2 | HG02165.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.645+1681_645+1682i others(158): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852309 | |||||
| chr16:89852309
|
A | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0083others(133): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.645+1649A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852309 | ||||||
| chr16:89852310
|
T | C | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.645+1650T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852310 | ||||||
| chr16:89852310
|
T | TGGCCCAT others(811): Show |
1 | a0001c0001t0001g0063 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.645+1675_645+1676i others(820): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852310 | |||||
| chr16:89852312
|
G | GCCCATCT others(8): Show |
1 | a0001c0001t0001g0002 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.645+1656_645+1670d others(17): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852312 | |||||
| chr16:89852313
|
C | CCCGTCTT others(73): Show |
1 | a0001c0003t0005g0275 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.645+1655_645+1656i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852313 | |||||
| chr16:89852316
|
A | G | 20 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0115others(17): Show | 20 | HG01071.hp1 HG01099.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.645+1656A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852316 | ||||||
| chr16:89852323
|
A | G | 14 | a0001c0001t0001g0134a0001c0001t0001g0141a0001c0001t0001g0145others(11): Show | 14 | HG02258.hp2 HG02572.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.645+1663A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852323 | ||||||
| chr16:89852326
|
C | T | 1 | a0001c0006t0001g0012 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.645+1666C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852326 | ||||||
| chr16:89852327
|
T | C | 1 | a0001c0006t0001g0012 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.645+1667T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852327 | ||||||
| chr16:89852328
|
C | CCCCCCAC others(421): Show |
1 | a0001c0001t0001g0060 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.645+1681_645+1682i others(430): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852328 | |||||
| chr16:89852329
|
C | T | 14 | a0001c0001t0001g0104a0001c0001t0001g0134a0001c0001t0001g0158others(11): Show | 14 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.645+1669C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852329 | ||||||
| chr16:89852330
|
C | CT | 6 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0147others(3): Show | 6 | HG02622.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.645+1670_645+1671i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852330 | ||||||
| chr16:89852330
|
C | CTCTCACC others(554): Show |
1 | a0010c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.645+1670_645+1671i others(563): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852330 | ||||||
| chr16:89852330
|
C | T | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645+1670C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852330 | ||||||
| chr16:89852331
|
C | T | 10 | a0001c0001t0001g0083a0001c0001t0001g0105a0001c0001t0001g0106others(7): Show | 10 | HG01516.hp2 HG02683.hp2 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.645+1671C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852331 | ||||||
| chr16:89852332
|
C | A | 1 | a0001c0006t0001g0012 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.645+1672C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852332 | ||||||
| chr16:89852332
|
C | T | 8 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0147others(5): Show | 8 | HG02622.hp1 HG02717.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.645+1672C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852332 | ||||||
| chr16:89852333
|
C | A | 44 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0115others(41): Show | 44 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.645+1673C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852333 | ||||||
| chr16:89852338
|
C | A | 85 | a0001c0001t0001g0006a0001c0001t0001g0054a0001c0001t0001g0087others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.645+1678C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852338 | ||||||
| chr16:89852338
|
C | CCCAGATC others(1240): Show |
1 | a0001c0001t0001g0080 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.645+1681_645+1682i others(1249): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852338 | |||||
| chr16:89852338
|
C | G | 13 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0115others(10): Show | 13 | HG01071.hp1 HG01106.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.645+1678C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852338 | ||||||
| chr16:89852340
|
C | T | 11 | a0001c0001t0001g0104a0001c0001t0001g0134a0001c0001t0001g0158others(8): Show | 11 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.645+1680C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852340 | ||||||
| chr16:89852341
|
A | G | 30 | a0001c0001t0001g0083a0001c0001t0001g0104a0001c0001t0001g0105others(27): Show | 30 | HG01081.hp1 HG01516.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.645+1681A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852341 | ||||||
| chr16:89852342
|
T | C | 2 | a0001c0001t0001g0145a0006c0010t0001g0314 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.645+1682T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852342 | ||||||
| chr16:89852342
|
T | G | 291 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.645+1682T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852342 | ||||||
| chr16:89852345
|
T | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.645+1685T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852345 | ||||||
| chr16:89852348
|
A | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0056others(156): Show | 159 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.645+1688A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852348 | ||||||
| chr16:89852349
|
T | C | 2 | a0001c0001t0001g0071a0001c0008t0001g0009 | 2 | HG00099.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.645+1689T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852349 | ||||||
| chr16:89852352
|
C | CCCGTCTT others(73): Show |
2 | a0001c0001t0001g0294a0003c0005t0001g0297 | 2 | HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.645+1694_645+1695i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852352 | |||||
| chr16:89852352
|
C | CCCGTCTT others(193): Show |
3 | a0003c0005t0001g0296a0003c0005t0001g0298a0003c0005t0001g0299 | 3 | HG01167.hp1 HG01169.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.645+1694_645+1695i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852352 | |||||
| chr16:89852352
|
C | CCCGTCTT others(393): Show |
1 | a0001c0001t0001g0351 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.645+1694_645+1695i others(402): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852352 | |||||
| chr16:89852355
|
A | G | 33 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0147others(30): Show | 33 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(30): Show |
intron_variant | MODIFIER | c.645+1695A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852355 | ||||||
| chr16:89852358
|
T | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0160others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1698T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852358 | ||||||
| chr16:89852362
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0105others(48): Show | 51 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.645+1702A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852362 | ||||||
| chr16:89852365
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0160others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1705C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852365 | ||||||
| chr16:89852367
|
C | CT | 4 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0160others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1707_645+1708i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852367 | ||||||
| chr16:89852368
|
C | CCCCCACC others(1163): Show |
1 | a0001c0011t0001g0318 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.645+1720_645+1721i others(1172): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852368 | |||||
| chr16:89852368
|
C | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0058others(23): Show | 26 | HG00621.hp1 HG01243.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.645+1708C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852368 | ||||||
| chr16:89852369
|
C | CT | 26 | a0001c0001t0001g0145a0001c0001t0001g0290a0001c0001t0001g0294others(23): Show | 26 | HG00280.hp1 HG00408.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.645+1709_645+1710i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852369 | ||||||
| chr16:89852369
|
C | CTCTCACC others(114): Show |
5 | a0001c0001t0001g0293a0001c0001t0001g0305a0001c0001t0001g0347others(2): Show | 5 | HG00733.hp1 HG00735.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.645+1709_645+1710i others(123): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852369 | ||||||
| chr16:89852369
|
C | CTCTCACC others(234): Show |
2 | a0001c0001t0010g0348a0003c0005t0001g0304 | 2 | HG01099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.645+1709_645+1710i others(243): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852369 | ||||||
| chr16:89852369
|
C | CTCTCACC others(354): Show |
1 | a0001c0001t0001g0349 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.645+1709_645+1710i others(363): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852369 | ||||||
| chr16:89852369
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0160others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1709C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852369 | ||||||
| chr16:89852370
|
C | T | 20 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(17): Show | 20 | HG00621.hp2 HG00673.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.645+1710C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852370 | ||||||
| chr16:89852371
|
C | CAACCCCC others(193): Show |
1 | a0001c0001t0001g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.645+1711_645+1712i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852371 | ||||||
| chr16:89852371
|
C | T | 38 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0147others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.645+1711C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852371 | ||||||
| chr16:89852372
|
C | A | 23 | a0001c0001t0001g0099a0001c0001t0001g0178a0001c0001t0001g0179others(20): Show | 23 | HG00099.hp1 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.645+1712C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852372 | ||||||
| chr16:89852377
|
C | A | 12 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0001t0001g0081others(9): Show | 12 | HG00733.hp2 HG01081.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.645+1717C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852377 | ||||||
| chr16:89852377
|
C | CCCAGATC others(32): Show |
1 | a0001c0001t0001g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.645+1755_645+1756i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCAGATC others(32): Show |
1 | a0001c0001t0001g0190 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.645+1746_645+1747i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCAGATC others(32): Show |
3 | a0001c0001t0001g0100a0001c0001t0001g0177a0001c0001t0001g0253 | 3 | HG01934.hp2 HG02083.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.645+1726_645+1727i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCAGATC others(422): Show |
1 | a0001c0001t0001g0234 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.645+1726_645+1727i others(431): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(2271): Show |
1 | a0001c0001t0001g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.645+1720_645+1721i others(2280): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(2428): Show |
1 | a0001c0001t0001g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.645+1720_645+1721i others(2437): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(2428): Show |
1 | a0001c0001t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.645+1720_645+1721i others(2437): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(501): Show |
1 | a0001c0021t0001g0065 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.645+1720_645+1721i others(510): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(267): Show |
3 | a0001c0001t0001g0066a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG00642.hp2 HG00735.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.645+1720_645+1721i others(276): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(267): Show |
1 | a0001c0001t0001g0067 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.645+1720_645+1721i others(276): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(306): Show |
6 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0079others(3): Show | 6 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.645+1720_645+1721i others(315): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(618): Show |
1 | a0001c0001t0001g0086 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.645+1720_645+1721i others(627): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(306): Show |
1 | a0001c0001t0006g0070 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.645+1720_645+1721i others(315): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(384): Show |
4 | a0001c0001t0001g0059a0001c0001t0001g0069a0001c0001t0001g0075others(1): Show | 4 | HG01070.hp1 HG01074.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+1720_645+1721i others(393): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(345): Show |
1 | a0001c0001t0001g0085 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.645+1720_645+1721i others(354): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(307): Show |
1 | a0001c0001t0001g0094 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.645+1720_645+1721i others(316): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | CCCATATT others(307): Show |
1 | a0001c0001t0001g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.645+1720_645+1721i others(316): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852377 | |||||
| chr16:89852377
|
C | G | 10 | a0001c0001t0001g0099a0001c0001t0001g0178a0001c0001t0001g0179others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.645+1717C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852377 | ||||||
| chr16:89852379
|
C | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0105others(15): Show | 18 | HG01243.hp2 HG01516.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.645+1719C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852379 | ||||||
| chr16:89852380
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0105others(80): Show | 83 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.645+1720A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852380 | ||||||
| chr16:89852381
|
G | C | 2 | a0001c0001t0010g0348a0003c0005t0001g0304 | 2 | HG01099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.645+1721G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852381 | ||||||
| chr16:89852381
|
G | GATCCCAT others(233): Show |
1 | a0001c0001t0001g0307 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.645+1733_645+1734i others(242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852381 | |||||
| chr16:89852381
|
G | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0062others(53): Show | 56 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.645+1721G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852381 | ||||||
| chr16:89852384
|
C | CCCATGGC others(228): Show |
1 | a0001c0001t0003g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.645+1746_645+1747i others(237): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852384 | |||||
| chr16:89852384
|
C | CCCATGGC others(227): Show |
5 | a0001c0001t0003g0320a0001c0001t0003g0330a0001c0001t0003g0341others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.645+1746_645+1747i others(236): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852384 | |||||
| chr16:89852384
|
C | CCCATGGC others(227): Show |
1 | a0001c0001t0003g0340 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.645+1746_645+1747i others(236): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852384 | |||||
| chr16:89852384
|
C | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0062others(54): Show | 57 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.645+1724C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852384 | ||||||
| chr16:89852387
|
A | ATGGCCCA others(32): Show |
1 | a0001c0001t0004g0316 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.645+1750_645+1751i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852387 | |||||
| chr16:89852387
|
A | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0068others(82): Show | 85 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.645+1727A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852387 | ||||||
| chr16:89852390
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0160others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1730G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852390 | ||||||
| chr16:89852391
|
C | CCCGTCAT others(33): Show |
7 | a0001c0001t0001g0290a0001c0001t0001g0327a0001c0001t0001g0352others(4): Show | 7 | HG00280.hp1 HG01243.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.645+1733_645+1734i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852391 | |||||
| chr16:89852391
|
C | CCCGTCTT others(73): Show |
3 | a0001c0001t0001g0289a0001c0001t0001g0306a0001c0001t0001g0308 | 3 | HG01109.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.645+1733_645+1734i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852391 | |||||
| chr16:89852391
|
C | CCCGTCTT others(193): Show |
1 | a0001c0003t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.645+1733_645+1734i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852391 | |||||
| chr16:89852391
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0160others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1731C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852391 | ||||||
| chr16:89852394
|
A | G | 40 | a0001c0001t0001g0134a0001c0001t0001g0145a0001c0001t0001g0150others(37): Show | 40 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.645+1734A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852394 | ||||||
| chr16:89852397
|
T | A | 4 | a0001c0001t0001g0353a0004c0004t0001g0173a0004c0004t0001g0194others(1): Show | 4 | HG00408.hp1 HG02300.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+1737T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852397 | ||||||
| chr16:89852401
|
A | G | 56 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(53): Show | 56 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.645+1741A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852401 | ||||||
| chr16:89852404
|
C | T | 13 | a0001c0001t0001g0145a0001c0001t0001g0347a0001c0001t0001g0353others(10): Show | 13 | HG00408.hp1 HG00733.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.645+1744C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852404 | ||||||
| chr16:89852406
|
C | CT | 14 | a0001c0001t0001g0145a0001c0001t0001g0347a0001c0001t0001g0353others(11): Show | 14 | HG00408.hp1 HG00733.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.645+1746_645+1747i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852406 | ||||||
| chr16:89852407
|
C | T | 27 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(24): Show | 27 | HG00621.hp2 HG00673.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.645+1747C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852407 | ||||||
| chr16:89852408
|
C | CT | 40 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0150others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.645+1748_645+1749i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852408 | ||||||
| chr16:89852408
|
C | T | 13 | a0001c0001t0001g0145a0001c0001t0001g0347a0001c0001t0001g0353others(10): Show | 13 | HG00408.hp1 HG00733.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.645+1748C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852408 | ||||||
| chr16:89852409
|
C | T | 15 | a0001c0001t0001g0083a0001c0001t0001g0108a0001c0001t0001g0112others(12): Show | 15 | HG00741.hp1 HG01891.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.645+1749C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852409 | ||||||
| chr16:89852410
|
C | T | 53 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0147others(50): Show | 53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.645+1750C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852410 | ||||||
| chr16:89852411
|
C | A | 23 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0105others(20): Show | 23 | HG01071.hp1 HG01106.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.645+1751C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852411 | ||||||
| chr16:89852411
|
C | CACCCGCC others(71): Show |
1 | a0001c0001t0001g0057 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.645+1755_645+1756i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852411 | |||||
| chr16:89852416
|
C | A | 25 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0134others(22): Show | 25 | HG00621.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.645+1756C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852416 | ||||||
| chr16:89852416
|
C | CCCAGATC others(781): Show |
1 | a0004c0004t0001g0197 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.645+1785_645+1786i others(790): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852416 | |||||
| chr16:89852416
|
C | G | 13 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0001t0001g0084others(10): Show | 13 | HG01071.hp1 HG01106.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.645+1756C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852416 | ||||||
| chr16:89852417
|
C | G | 1 | a0004c0004t0001g0186 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.645+1757C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852417 | ||||||
| chr16:89852418
|
C | T | 18 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(15): Show | 18 | HG00621.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.645+1758C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852418 | ||||||
| chr16:89852419
|
A | G | 103 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.645+1759A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852419 | ||||||
| chr16:89852419
|
AGATCCCA others(149): Show |
A | 1 | a0001c0001t0001g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.645+1766_646-1705d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852419 | |||||
| chr16:89852420
|
G | C | 3 | a0001c0001t0001g0293a0001c0001t0001g0305a0001c0003t0001g0121 | 3 | HG00735.hp2 HG01123.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.645+1760G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852420 | ||||||
| chr16:89852420
|
G | GATCCCCT others(193): Show |
1 | a0001c0001t0001g0083 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.645+1765_645+1766i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852420 | |||||
| chr16:89852420
|
G | T | 1 | a0002c0002t0002g0023 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.645+1760G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852420 | ||||||
| chr16:89852423
|
C | T | 7 | a0002c0002t0002g0023a0002c0002t0002g0024a0002c0002t0002g0031others(4): Show | 7 | HG00323.hp1 HG02015.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.645+1763C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852423 | ||||||
| chr16:89852426
|
A | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(129): Show | 132 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.645+1766A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852426 | ||||||
| chr16:89852429
|
G | A | 15 | a0001c0001t0001g0145a0001c0001t0001g0321a0001c0001t0001g0322others(12): Show | 15 | HG00408.hp1 HG00733.hp1 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.645+1769G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852429 | ||||||
| chr16:89852430
|
C | T | 15 | a0001c0001t0001g0145a0001c0001t0001g0321a0001c0001t0001g0322others(12): Show | 15 | HG00408.hp1 HG00733.hp1 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.645+1770C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852430 | ||||||
| chr16:89852433
|
A | C | 1 | a0001c0001t0001g0083 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.645+1773A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852433 | ||||||
| chr16:89852433
|
A | G | 47 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(44): Show | 47 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.645+1773A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852433 | ||||||
| chr16:89852436
|
T | A | 8 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(5): Show | 8 | HG00099.hp1 HG01993.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.645+1776T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852436 | ||||||
| chr16:89852440
|
A | ATCCTCCC others(32): Show |
1 | a0001c0001t0001g0264 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.645+1785_645+1786i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852440 | |||||
| chr16:89852440
|
A | ATCCTCTC others(1593): Show |
1 | a0001c0001t0001g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.646-1783_646-1782i others(1602): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852440 | |||||
| chr16:89852440
|
A | G | 56 | a0001c0001t0001g0083a0001c0001t0001g0105a0001c0001t0001g0106others(53): Show | 56 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.645+1780A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852440 | ||||||
| chr16:89852441
|
T | TCCTCCCT others(33): Show |
1 | a0001c0001t0001g0247 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.645+1785_645+1786i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852441 | |||||
| chr16:89852443
|
C | T | 13 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG00099.hp1 HG00323.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.645+1783C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852443 | ||||||
| chr16:89852444
|
T | TCCCTCTC others(351): Show |
1 | a0001c0001t0001g0130 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.645+1785_645+1786i others(360): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852444 | |||||
| chr16:89852444
|
T | TCCCTCTC others(391): Show |
2 | a0001c0001t0001g0129a0001c0003t0001g0165 | 2 | HG01516.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.645+1785_645+1786i others(400): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852444 | |||||
| chr16:89852445
|
CTCCCCAC others(106): Show |
C | 2 | a0004c0004t0001g0173a0004c0004t0001g0196 | 2 | HG00408.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.645+1786_646-1728d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852445 | ||||||
| chr16:89852446
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(212): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.645+1786T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852446 | ||||||
| chr16:89852447
|
C | CT | 57 | a0001c0001t0001g0083a0001c0001t0001g0105a0001c0001t0001g0106others(54): Show | 57 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.645+1787_645+1788i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852447 | ||||||
| chr16:89852448
|
C | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0084others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.645+1788C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852448 | ||||||
| chr16:89852449
|
C | CTCT | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0003t0001g0165 | 3 | HG01516.hp2 HG02683.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.645+1789_645+1790i others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852449 | ||||||
| chr16:89852449
|
C | T | 57 | a0001c0001t0001g0083a0001c0001t0001g0105a0001c0001t0001g0106others(54): Show | 57 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.645+1789C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852449 | ||||||
| chr16:89852450
|
C | A | 22 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(19): Show | 22 | HG00621.hp2 HG00673.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.645+1790C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852450 | ||||||
| chr16:89852455
|
A | ACCAGATC others(71): Show |
1 | a0001c0001t0001g0151 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.646-1783_646-1782i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852455 | |||||
| chr16:89852455
|
A | ACCAGATC others(346): Show |
1 | a0001c0001t0001g0064 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.646-1783_646-1782i others(355): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852455 | |||||
| chr16:89852455
|
A | ACCAGATC others(189): Show |
1 | a0001c0001t0001g0089 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.646-1783_646-1782i others(198): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852455 | |||||
| chr16:89852455
|
A | ACCAGATC others(423): Show |
1 | a0001c0001t0001g0062 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.646-1783_646-1782i others(432): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852455 | |||||
| chr16:89852455
|
A | C | 241 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0058others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.645+1795A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852455 | ||||||
| chr16:89852455
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.645+1795A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852455 | ||||||
| chr16:89852457
|
C | T | 12 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0162others(9): Show | 12 | HG01256.hp2 HG01891.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.645+1797C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852457 | ||||||
| chr16:89852458
|
A | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0083others(149): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.645+1798A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852458 | ||||||
| chr16:89852459
|
G | C | 10 | a0001c0001t0001g0129a0001c0001t0001g0141a0001c0001t0001g0147others(7): Show | 10 | HG01099.hp2 HG01516.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.645+1799G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852459 | ||||||
| chr16:89852459
|
G | T | 2 | a0005c0007t0002g0032a0005c0007t0002g0036 | 2 | HG01175.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.645+1799G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852459 | ||||||
| chr16:89852462
|
C | CCCATGGC others(227): Show |
1 | a0001c0001t0003g0333 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.646-1802_646-1801i others(236): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852462 | |||||
| chr16:89852462
|
C | T | 22 | a0002c0002t0002g0022a0002c0002t0002g0025a0002c0002t0002g0027others(19): Show | 22 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.645+1802C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852462 | ||||||
| chr16:89852465
|
A | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0057others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.645+1805A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852465 | ||||||
| chr16:89852466
|
T | C | 2 | a0005c0014t0002g0021a0016c0015t0002g0049 | 2 | HG00621.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.645+1806T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852466 | ||||||
| chr16:89852468
|
G | A | 13 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG00099.hp1 HG00323.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.645+1808G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852468 | ||||||
| chr16:89852469
|
C | CCCGTCAT others(33): Show |
3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0167 | 3 | HG03491.hp1 NA18993.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.645+1811_645+1812i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852469 | |||||
| chr16:89852469
|
C | CCCGTCAT others(153): Show |
1 | a0001c0001t0001g0166 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.645+1811_645+1812i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852469 | |||||
| chr16:89852469
|
C | CCCGTCTT others(73): Show |
6 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0127others(3): Show | 6 | HG01928.hp2 HG01943.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.645+1811_645+1812i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852469 | |||||
| chr16:89852469
|
C | CCCGTCTT others(193): Show |
3 | a0001c0001t0001g0114a0001c0001t0001g0123a0001c0001t0007g0026 | 3 | HG02027.hp2 NA18960.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.645+1811_645+1812i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852469 | |||||
| chr16:89852469
|
C | CCCGTCTT others(353): Show |
1 | a0001c0001t0001g0110 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.645+1811_645+1812i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852469 | |||||
| chr16:89852469
|
C | CCCGTCTT others(433): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0111 | 2 | NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.645+1811_645+1812i others(442): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852469 | |||||
| chr16:89852469
|
C | T | 13 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG00099.hp1 HG00323.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.645+1809C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852469 | ||||||
| chr16:89852472
|
A | G | 56 | a0001c0001t0001g0083a0001c0001t0001g0113a0001c0001t0001g0129others(53): Show | 56 | HG00280.hp1 HG00621.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.645+1812A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852472 | ||||||
| chr16:89852475
|
T | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0291 | 2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.646-1811T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852475 | ||||||
| chr16:89852479
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0084others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.646-1807A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852479 | ||||||
| chr16:89852482
|
C | T | 9 | a0001c0001t0001g0113a0001c0001t0001g0291a0001c0001t0001g0321others(6): Show | 9 | HG00280.hp1 HG01243.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1804C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852482 | ||||||
| chr16:89852484
|
C | CT | 9 | a0001c0001t0001g0113a0001c0001t0001g0291a0001c0001t0001g0321others(6): Show | 9 | HG00280.hp1 HG01243.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1802_646-1801i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852484 | ||||||
| chr16:89852485
|
C | CCCCCACC others(812): Show |
3 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286 | 3 | HG02257.hp2 HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.646-1783_646-1782i others(821): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852485 | |||||
| chr16:89852485
|
C | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0084others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.646-1801C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852485 | ||||||
| chr16:89852486
|
C | CT | 65 | a0001c0001t0001g0083a0001c0001t0001g0105a0001c0001t0001g0106others(62): Show | 65 | HG00099.hp1 HG00323.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.646-1800_646-1799i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852486 | ||||||
| chr16:89852486
|
C | CTCTCACC others(74): Show |
1 | a0001c0001t0001g0141 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.646-1800_646-1799i others(83): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852486 | ||||||
| chr16:89852486
|
C | CTCTCACC others(194): Show |
2 | a0001c0001t0001g0231a0001c0001t0001g0245 | 2 | NA18949.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.646-1800_646-1799i others(203): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852486 | ||||||
| chr16:89852486
|
C | CTCTCACC others(234): Show |
1 | a0004c0004t0001g0186 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.646-1800_646-1799i others(243): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852486 | ||||||
| chr16:89852486
|
C | CTCTCACC others(354): Show |
1 | a0001c0001t0002g0122 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.646-1800_646-1799i others(363): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852486 | ||||||
| chr16:89852486
|
C | T | 10 | a0001c0001t0001g0113a0001c0001t0001g0291a0001c0001t0001g0321others(7): Show | 10 | HG00280.hp1 HG01243.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.646-1800C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852486 | ||||||
| chr16:89852487
|
C | T | 9 | a0001c0001t0001g0134a0001c0001t0001g0191a0001c0001t0001g0210others(6): Show | 9 | HG00408.hp2 HG02622.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1799C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852487 | ||||||
| chr16:89852488
|
C | T | 80 | a0001c0001t0001g0083a0001c0001t0001g0105a0001c0001t0001g0106others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.646-1798C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852488 | ||||||
| chr16:89852489
|
C | A | 16 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0162others(13): Show | 16 | HG00741.hp1 HG01175.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.646-1797C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852489 | ||||||
| chr16:89852489
|
C | CACCCCCC others(773): Show |
1 | a0001c0001t0001g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.646-1783_646-1782i others(782): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852489 | |||||
| chr16:89852489
|
C | CACCCCCC others(1202): Show |
1 | a0001c0001t0001g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.646-1783_646-1782i others(1211): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852489 | |||||
| chr16:89852494
|
C | A | 23 | a0001c0001t0001g0087a0001c0001t0001g0287a0001c0001t0001g0324others(20): Show | 23 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.646-1792C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852494 | ||||||
| chr16:89852495
|
C | G | 2 | a0004c0004t0001g0187a0004c0004t0001g0205 | 2 | NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.646-1791C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852495 | ||||||
| chr16:89852496
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0084others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.646-1790C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852496 | ||||||
| chr16:89852497
|
A | ATATTCCA others(578): Show |
1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.646-1789_646-1788i others(587): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852497 | ||||||
| chr16:89852497
|
A | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0083others(166): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.646-1789A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852497 | ||||||
| chr16:89852498
|
G | C | 24 | a0001c0001t0001g0083a0001c0001t0001g0145a0001c0001t0001g0147others(21): Show | 24 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.646-1788G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852498 | ||||||
| chr16:89852498
|
G | T | 2 | a0005c0014t0002g0021a0016c0015t0002g0049 | 2 | HG00621.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.646-1788G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852498 | ||||||
| chr16:89852501
|
C | T | 2 | a0005c0014t0002g0021a0016c0015t0002g0049 | 2 | HG00621.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.646-1785C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852501 | ||||||
| chr16:89852504
|
A | ATGGCCCA others(71): Show |
1 | a0001c0001t0001g0063 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.646-1763_646-1762i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852504 | |||||
| chr16:89852504
|
A | ATGGCCCA others(711): Show |
1 | a0001c0008t0001g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.646-1763_646-1762i others(720): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852504 | |||||
| chr16:89852504
|
A | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0054others(95): Show | 98 | HG00099.hp2 HG00408.hp2 HG00741.hp1 others(95): Show |
intron_variant | MODIFIER | c.646-1782A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852504 | ||||||
| chr16:89852505
|
T | C | 5 | a0001c0001t0001g0337a0002c0002t0002g0024a0002c0002t0002g0053others(2): Show | 5 | HG01109.hp2 HG02080.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1781T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852505 | ||||||
| chr16:89852507
|
G | A | 10 | a0001c0001t0001g0113a0001c0001t0001g0141a0001c0001t0001g0291others(7): Show | 10 | HG00280.hp1 HG01243.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.646-1779G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852507 | ||||||
| chr16:89852508
|
C | CCCGTCAT others(33): Show |
1 | a0001c0001t0002g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.646-1776_646-1775i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852508 | |||||
| chr16:89852508
|
C | CCCGTCTT others(73): Show |
1 | a0001c0001t0001g0350 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.646-1776_646-1775i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852508 | |||||
| chr16:89852508
|
C | T | 10 | a0001c0001t0001g0113a0001c0001t0001g0141a0001c0001t0001g0291others(7): Show | 10 | HG00280.hp1 HG01243.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.646-1778C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852508 | ||||||
| chr16:89852511
|
A | G | 81 | a0001c0001t0001g0083a0001c0001t0001g0105a0001c0001t0001g0106others(78): Show | 81 | HG00099.hp1 HG00323.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.646-1775A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852511 | ||||||
| chr16:89852514
|
T | A | 6 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(3): Show | 6 | NA18949.hp1 NA18951.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1772T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852514 | ||||||
| chr16:89852517
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.646-1769C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852517 | ||||||
| chr16:89852518
|
A | ATCCTCCC others(384): Show |
1 | a0001c0001t0001g0077 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.646-1759_646-1758i others(393): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852518 | |||||
| chr16:89852518
|
A | ATCCTCCC others(384): Show |
1 | a0001c0001t0001g0082 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.646-1759_646-1758i others(393): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852518 | |||||
| chr16:89852518
|
A | ATCCTCTC others(71): Show |
4 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00642.hp1 HG01123.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1763_646-1762i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852518 | |||||
| chr16:89852518
|
A | G | 87 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0108others(84): Show | 87 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.646-1768A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852518 | ||||||
| chr16:89852521
|
C | T | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0353others(2): Show | 5 | HG02300.hp2 NA18951.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1765C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852521 | ||||||
| chr16:89852524
|
C | T | 18 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(15): Show | 18 | HG01081.hp1 HG01175.hp1 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.646-1762C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852524 | ||||||
| chr16:89852526
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0060others(136): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.646-1760T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852526 | ||||||
| chr16:89852526
|
T | TCTCACCC others(825): Show |
2 | a0001c0008t0001g0008a0001c0008t0001g0011 | 2 | HG01167.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.646-1759_646-1758i others(834): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852526 | |||||
| chr16:89852526
|
T | TCTCACCC others(666): Show |
1 | a0001c0008t0001g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.646-1759_646-1758i others(675): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852526 | |||||
| chr16:89852527
|
C | CCACCCCC others(1032): Show |
1 | a0001c0001t0001g0328 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.646-1751_646-1750i others(1041): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | |||||
| chr16:89852527
|
C | CCACCCCC others(832): Show |
1 | a0001c0001t0003g0329 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.646-1751_646-1750i others(841): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | |||||
| chr16:89852527
|
C | CCACCCCC others(1152): Show |
1 | a0001c0001t0003g0345 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.646-1751_646-1750i others(1161): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | |||||
| chr16:89852527
|
C | CCACCCCC others(1192): Show |
1 | a0001c0001t0003g0335 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.646-1751_646-1750i others(1201): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | |||||
| chr16:89852527
|
C | CCACCCCC others(1112): Show |
1 | a0001c0001t0003g0325 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.646-1751_646-1750i others(1121): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | |||||
| chr16:89852527
|
C | CCACCCCC others(1112): Show |
1 | a0001c0001t0003g0326 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.646-1751_646-1750i others(1121): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | |||||
| chr16:89852527
|
C | CT | 91 | a0001c0001t0001g0083a0001c0001t0001g0105a0001c0001t0001g0106others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.646-1759_646-1758i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852527 | ||||||
| chr16:89852527
|
C | CTCACCCC others(891): Show |
3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.646-1759_646-1758i others(900): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852527 | ||||||
| chr16:89852527
|
C | CTCACCCC others(874): Show |
1 | a0001c0001t0003g0334 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.646-1759_646-1758i others(883): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852527 | ||||||
| chr16:89852527
|
CCACCCCC others(70): Show |
C | 1 | a0001c0001t0001g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.646-1757_646-1681d others(79): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852527 | |||||
| chr16:89852528
|
C | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0084others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.646-1758C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852528 | ||||||
| chr16:89852528
|
C | CACCCCCC others(227): Show |
1 | a0002c0002t0002g0022 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.646-1751_646-1750i others(236): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852528 | |||||
| chr16:89852528
|
C | CACCCCCC others(71): Show |
13 | a0002c0002t0002g0027a0002c0002t0002g0028a0002c0002t0002g0029others(10): Show | 13 | HG00438.hp2 HG00597.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.646-1751_646-1750i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852528 | |||||
| chr16:89852528
|
C | CACCCCCC others(188): Show |
1 | a0009c0025t0002g0039 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.646-1751_646-1750i others(197): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852528 | |||||
| chr16:89852528
|
C | CACCCCCC others(266): Show |
1 | a0002c0002t0002g0034 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.646-1751_646-1750i others(275): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852528 | |||||
| chr16:89852528
|
C | CACCCCCC others(32): Show |
5 | a0002c0002t0002g0024a0002c0002t0002g0031a0002c0002t0002g0053others(2): Show | 5 | HG02015.hp1 HG02080.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1751_646-1750i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852528 | |||||
| chr16:89852528
|
C | CACCCCCC others(72): Show |
1 | a0002c0002t0014g0044 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.646-1751_646-1750i others(81): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852528 | |||||
| chr16:89852533
|
C | A | 2 | a0002c0002t0002g0025a0002c0002t0002g0050 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.646-1753C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852533 | ||||||
| chr16:89852533
|
C | CCCATATT others(539): Show |
1 | a0001c0001t0001g0176 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.646-1751_646-1750i others(548): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852533 | |||||
| chr16:89852535
|
C | T | 9 | a0001c0001t0001g0134a0001c0001t0001g0210a0001c0001t0001g0232others(6): Show | 9 | HG01175.hp1 HG02148.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1751C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852535 | ||||||
| chr16:89852536
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0060others(132): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.646-1750G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852536 | ||||||
| chr16:89852537
|
G | C | 19 | a0001c0001t0001g0114a0001c0001t0001g0123a0001c0001t0001g0166others(16): Show | 19 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.646-1749G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852537 | ||||||
| chr16:89852537
|
G | T | 2 | a0001c0001t0003g0332a0001c0001t0003g0336 | 2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.646-1749G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852537 | ||||||
| chr16:89852540
|
C | CCCATGGC others(232): Show |
1 | a0001c0006t0001g0016 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.646-1744_646-1743i others(241): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852540 | |||||
| chr16:89852540
|
C | T | 2 | a0001c0001t0003g0332a0001c0001t0003g0336 | 2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.646-1746C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852540 | ||||||
| chr16:89852542
|
C | T | 12 | a0001c0001t0001g0337a0001c0001t0003g0320a0001c0001t0003g0323others(9): Show | 12 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.646-1744C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852542 | ||||||
| chr16:89852543
|
C | A | 120 | a0001c0001t0001g0060a0001c0001t0001g0083a0001c0001t0001g0089others(117): Show | 120 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.646-1743C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852543 | ||||||
| chr16:89852543
|
C | CTGGCCCA others(32): Show |
1 | a0001c0009t0001g0017 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.646-1730_646-1729i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852543 | |||||
| chr16:89852544
|
T | C | 1 | a0002c0002t0002g0045 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.646-1742T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852544 | ||||||
| chr16:89852546
|
G | A | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0353others(2): Show | 5 | HG02300.hp2 NA18951.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1740G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852546 | ||||||
| chr16:89852547
|
C | T | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0353others(2): Show | 5 | HG02300.hp2 NA18951.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1739C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852547 | ||||||
| chr16:89852550
|
A | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0072others(172): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.646-1736A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852550 | ||||||
| chr16:89852553
|
T | A | 13 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0162others(10): Show | 13 | HG00741.hp1 HG01891.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.646-1733T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852553 | ||||||
| chr16:89852557
|
G | A | 68 | a0001c0001t0001g0060a0001c0001t0001g0089a0001c0001t0001g0095others(65): Show | 68 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.646-1729G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852557 | ||||||
| chr16:89852557
|
GTCCTCTC others(32): Show |
G | 1 | a0003c0005t0001g0301 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.646-1723_646-1685d others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852557 | |||||
| chr16:89852560
|
C | T | 29 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0112others(26): Show | 29 | HG00741.hp1 HG01099.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.646-1726C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852560 | ||||||
| chr16:89852561
|
T | TCCCTCTC others(76): Show |
1 | a0004c0004t0001g0271 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.646-1724_646-1723i others(85): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(71): Show |
1 | a0001c0001t0001g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.646-1724_646-1723i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(71): Show |
44 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0168others(41): Show | 44 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.646-1724_646-1723i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(111): Show |
2 | a0001c0001t0001g0260a0001c0001t0004g0208 | 2 | NA18947.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.646-1724_646-1723i others(120): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(312): Show |
1 | a0001c0001t0001g0256 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.646-1724_646-1723i others(321): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(151): Show |
1 | a0001c0001t0001g0199 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.646-1724_646-1723i others(160): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(311): Show |
2 | a0004c0004t0001g0187a0004c0004t0001g0205 | 2 | NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.646-1724_646-1723i others(320): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(551): Show |
1 | a0001c0001t0001g0254 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.646-1724_646-1723i others(560): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(191): Show |
5 | a0001c0001t0001g0181a0001c0001t0001g0219a0001c0001t0001g0236others(2): Show | 5 | HG01256.hp1 HG02572.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1724_646-1723i others(200): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(471): Show |
1 | a0001c0001t0001g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.646-1724_646-1723i others(480): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(871): Show |
1 | a0001c0001t0001g0302 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.646-1724_646-1723i others(880): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(871): Show |
1 | a0001c0001t0001g0303 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.646-1724_646-1723i others(880): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(110): Show |
1 | a0001c0001t0001g0169 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.646-1724_646-1723i others(119): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852561
|
T | TCCCTCTC others(71): Show |
4 | a0001c0001t0001g0113a0001c0001t0001g0206a0001c0001t0001g0291others(1): Show | 4 | HG00673.hp1 HG03017.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1724_646-1723i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852561 | |||||
| chr16:89852563
|
T | C | 112 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0084others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.646-1723T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852563 | ||||||
| chr16:89852563
|
T | TCCCCACC others(71): Show |
1 | a0001c0009t0001g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.646-1713_646-1712i others(80): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852563 | |||||
| chr16:89852564
|
C | CT | 104 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0084others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.646-1722_646-1721i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852564 | ||||||
| chr16:89852564
|
C | CTCTCACC others(34): Show |
4 | a0001c0001t0001g0147a0001c0001t0001g0202a0001c0001t0001g0240others(1): Show | 4 | HG02135.hp1 HG02970.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-1722_646-1721i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852564 | ||||||
| chr16:89852565
|
C | T | 7 | a0001c0001t0001g0089a0001c0001t0001g0135a0001c0006t0001g0012others(4): Show | 7 | HG02896.hp1 HG02897.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.646-1721C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852565 | ||||||
| chr16:89852566
|
C | CCACCCCC others(1193): Show |
1 | a0001c0001t0003g0332 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.646-1713_646-1712i others(1202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852566 | |||||
| chr16:89852566
|
C | CCACCCCC others(233): Show |
1 | a0001c0001t0003g0336 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.646-1713_646-1712i others(242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852566 | |||||
| chr16:89852566
|
C | CTCT | 65 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0115others(62): Show | 65 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.646-1720_646-1719i others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852566 | ||||||
| chr16:89852566
|
C | T | 108 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0084others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.646-1720C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852566 | ||||||
| chr16:89852567
|
C | A | 10 | a0001c0001t0001g0134a0001c0001t0001g0210a0001c0001t0001g0288others(7): Show | 10 | HG01175.hp1 HG02622.hp2 HG03834.hp1 others(7): Show |
intron_variant | MODIFIER | c.646-1719C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852567 | ||||||
| chr16:89852568
|
A | C | 2 | a0001c0006t0001g0012a0004c0004t0001g0271 | 2 | NA18951.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.646-1718A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852568 | ||||||
| chr16:89852572
|
C | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0176a0001c0001t0001g0305 | 3 | HG01123.hp2 HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.646-1714C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852572 | ||||||
| chr16:89852574
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(218): Show | 221 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.646-1712T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852574 | ||||||
| chr16:89852574
|
T | TGGATCCC others(507): Show |
1 | a0001c0001t0001g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.646-1705_646-1704i others(516): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852574 | |||||
| chr16:89852575
|
G | A | 34 | a0001c0001t0001g0060a0001c0001t0001g0095a0001c0001t0001g0096others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.646-1711G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852575 | ||||||
| chr16:89852575
|
G | GGATCCCC others(32): Show |
4 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00642.hp1 HG01123.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1683_646-1682i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852575 | |||||
| chr16:89852576
|
G | C | 30 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(27): Show | 30 | HG00280.hp1 HG00733.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.646-1710G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852576 | ||||||
| chr16:89852576
|
G | T | 3 | a0001c0001t0003g0333a0002c0002t0002g0030a0002c0002t0002g0045 | 3 | HG00609.hp1 HG02896.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.646-1710G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852576 | ||||||
| chr16:89852579
|
C | T | 3 | a0001c0001t0003g0333a0002c0002t0002g0030a0002c0002t0002g0045 | 3 | HG00609.hp1 HG02896.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.646-1707C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852579 | ||||||
| chr16:89852582
|
C | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.646-1704C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852582 | ||||||
| chr16:89852583
|
T | C | 1 | a0001c0006t0001g0016 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.646-1703T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852583 | ||||||
| chr16:89852583
|
T | TGGCCCAT others(351): Show |
1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.646-1691_646-1690i others(360): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852583 | |||||
| chr16:89852585
|
G | A | 25 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0112others(22): Show | 25 | HG00741.hp1 HG01099.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.646-1701G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852585 | ||||||
| chr16:89852586
|
C | CCCGTCAT others(33): Show |
7 | a0001c0001t0001g0184a0001c0001t0001g0192a0001c0001t0001g0220others(4): Show | 7 | HG02738.hp1 HG03654.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.646-1698_646-1697i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852586 | |||||
| chr16:89852586
|
C | CCCGTCTT others(73): Show |
1 | a0001c0001t0001g0006 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.646-1698_646-1697i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852586 | |||||
| chr16:89852586
|
C | CCCGTCTT others(393): Show |
1 | a0001c0001t0001g0288 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.646-1698_646-1697i others(402): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852586 | |||||
| chr16:89852586
|
C | T | 25 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0112others(22): Show | 25 | HG00741.hp1 HG01099.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.646-1700C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852586 | ||||||
| chr16:89852589
|
A | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0083a0001c0001t0001g0084others(149): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.646-1697A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852589 | ||||||
| chr16:89852592
|
T | A | 6 | a0001c0001t0001g0084a0001c0001t0001g0091a0001c0001t0001g0221others(3): Show | 6 | HG01106.hp1 HG02683.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1694T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852592 | ||||||
| chr16:89852596
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0083a0001c0001t0001g0084others(151): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.646-1690A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852596 | ||||||
| chr16:89852599
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0091a0001c0001t0001g0221others(2): Show | 5 | HG01106.hp1 HG02683.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-1687C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852599 | ||||||
| chr16:89852602
|
C | T | 9 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0091others(6): Show | 9 | HG01106.hp1 HG02683.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1684C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852602 | ||||||
| chr16:89852604
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0057others(103): Show | 106 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.646-1682T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852604 | ||||||
| chr16:89852604
|
T | TCCACCCC others(32): Show |
1 | a0001c0001t0001g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.646-1673_646-1672i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852604 | |||||
| chr16:89852605
|
C | CAACCCCC others(713): Show |
1 | a0002c0002t0002g0023 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.646-1681_646-1680i others(722): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852605 | ||||||
| chr16:89852605
|
C | CT | 188 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0083others(185): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.646-1681_646-1680i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852605 | ||||||
| chr16:89852605
|
C | CTCACCCC others(674): Show |
2 | a0005c0007t0002g0032a0005c0007t0002g0036 | 2 | HG01175.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.646-1681_646-1680i others(683): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852605 | ||||||
| chr16:89852605
|
C | CTCACCCC others(114): Show |
1 | a0001c0006t0001g0013 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.646-1681_646-1680i others(123): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852605 | ||||||
| chr16:89852605
|
C | CTCACCCC others(274): Show |
1 | a0011c0022t0001g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.646-1681_646-1680i others(283): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852605 | ||||||
| chr16:89852605
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.646-1681C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852605 | ||||||
| chr16:89852606
|
C | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0057others(89): Show | 92 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.646-1680C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852606 | ||||||
| chr16:89852606
|
C | CACCCCCC others(32): Show |
2 | a0001c0001t0001g0156a0001c0001t0001g0164 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.646-1673_646-1672i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852606 | |||||
| chr16:89852613
|
C | T | 4 | a0001c0001t0001g0089a0001c0001t0001g0135a0001c0001t0001g0149others(1): Show | 4 | HG02015.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1673C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852613 | ||||||
| chr16:89852614
|
A | AGATCCCA others(151): Show |
2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.646-1666_646-1665i others(160): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852614 | |||||
| chr16:89852614
|
A | ATATTCCA others(1113): Show |
1 | a0001c0001t0003g0333 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.646-1672_646-1671i others(1122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852614 | ||||||
| chr16:89852614
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0081others(193): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.646-1672A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852614 | ||||||
| chr16:89852615
|
G | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0083a0001c0001t0001g0105others(90): Show | 93 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.646-1671G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852615 | ||||||
| chr16:89852615
|
G | GATCCCAT others(1146): Show |
1 | a0002c0002t0002g0030 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.646-1666_646-1665i others(1155): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852615 | |||||
| chr16:89852618
|
C | CCCATGGC others(383): Show |
1 | a0001c0009t0001g0017 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.646-1666_646-1665i others(392): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852618 | |||||
| chr16:89852621
|
C | A | 191 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0060others(188): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.646-1665C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852621 | ||||||
| chr16:89852621
|
C | CTGGCCCA others(507): Show |
2 | a0002c0002t0002g0025a0002c0002t0002g0050 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.646-1659_646-1658i others(516): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | |||||
| chr16:89852621
|
C | CTGGCCCA others(32): Show |
1 | a0001c0009t0001g0019 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.646-1659_646-1658i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | |||||
| chr16:89852621
|
C | CTGGCCCG others(234): Show |
1 | a0002c0002t0002g0045 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.646-1633_646-1632i others(243): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | |||||
| chr16:89852621
|
C | CTGGCCCG others(232): Show |
1 | a0005c0007t0002g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.646-1623_646-1622i others(241): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | |||||
| chr16:89852621
|
C | CTGGCCCG others(233): Show |
3 | a0002c0002t0002g0024a0002c0002t0002g0031a0002c0002t0002g0037 | 3 | HG02015.hp1 NA18947.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.646-1623_646-1622i others(242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | |||||
| chr16:89852621
|
C | CTGGCCCG others(913): Show |
1 | a0002c0002t0002g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.646-1623_646-1622i others(922): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | |||||
| chr16:89852621
|
C | CTGGCCCG others(73): Show |
1 | a0001c0001t0001g0107 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.646-1619_646-1618i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | |||||
| chr16:89852621
|
C | CTGGCCCG others(113): Show |
1 | a0001c0001t0001g0069 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | |||||
| chr16:89852621
|
C | CTGGCCCG others(112): Show |
1 | a0001c0001t0001g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.646-1646_646-1645i others(121): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852621 | |||||
| chr16:89852624
|
G | A | 5 | a0001c0001t0001g0084a0001c0001t0001g0091a0001c0001t0001g0221others(2): Show | 5 | HG01106.hp1 HG02683.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-1662G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852624 | ||||||
| chr16:89852625
|
C | CCCATCTT others(424): Show |
1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.646-1659_646-1658i others(433): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852625 | |||||
| chr16:89852625
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0091a0001c0001t0001g0221others(2): Show | 5 | HG01106.hp1 HG02683.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-1661C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852625 | ||||||
| chr16:89852628
|
G | A | 20 | a0001c0001t0001g0060a0001c0001t0001g0077a0001c0001t0001g0082others(17): Show | 20 | HG00741.hp2 HG01074.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.646-1658G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852628 | ||||||
| chr16:89852628
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.646-1658G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852628 | ||||||
| chr16:89852631
|
T | A | 6 | a0001c0001t0001g0134a0001c0001t0001g0150a0001c0001t0001g0210others(3): Show | 6 | HG01106.hp2 HG02622.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1655T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852631 | ||||||
| chr16:89852635
|
G | A | 19 | a0001c0001t0001g0060a0001c0001t0001g0077a0001c0001t0001g0082others(16): Show | 19 | HG00741.hp2 HG01074.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.646-1651G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852635 | ||||||
| chr16:89852637
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0243 | 2 | HG02738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.646-1649C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852637 | ||||||
| chr16:89852638
|
C | T | 6 | a0001c0001t0001g0134a0001c0001t0001g0150a0001c0001t0001g0210others(3): Show | 6 | HG01106.hp2 HG02622.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1648C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852638 | ||||||
| chr16:89852641
|
C | T | 7 | a0001c0001t0001g0134a0001c0001t0001g0150a0001c0001t0001g0210others(4): Show | 7 | HG01106.hp2 HG02622.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.646-1645C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852641 | ||||||
| chr16:89852644
|
C | CCACCCCC others(70): Show |
1 | a0001c0001t0001g0082 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.646-1642_646-1641i others(79): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852644 | ||||||
| chr16:89852644
|
CT | C | 4 | a0001c0001t0001g0060a0001c0001t0001g0077a0001c0001t0001g0089others(1): Show | 4 | HG01074.hp1 HG01261.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1641delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852644 | ||||||
| chr16:89852645
|
T | C | 2 | a0001c0001t0001g0082a0001c0009t0001g0018 | 2 | HG00741.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.646-1641T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852645 | ||||||
| chr16:89852645
|
T | TCACCCCC others(32): Show |
1 | a0001c0001t0001g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.646-1634_646-1633i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852645 | |||||
| chr16:89852654
|
G | A | 9 | a0001c0001t0001g0077a0001c0001t0001g0081a0001c0001t0001g0082others(6): Show | 9 | HG00741.hp2 HG01074.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.646-1632G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852654 | ||||||
| chr16:89852654
|
G | GCATCCCA others(833): Show |
1 | a0001c0001t0001g0248 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.646-1632_646-1631i others(842): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852654 | ||||||
| chr16:89852655
|
G | C | 41 | a0001c0001t0001g0105a0001c0001t0001g0114a0001c0001t0001g0116others(38): Show | 41 | HG00735.hp2 HG01099.hp2 HG01928.hp2 others(38): Show |
intron_variant | MODIFIER | c.646-1631G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852655 | ||||||
| chr16:89852655
|
G | GATCCCAT others(593): Show |
2 | a0002c0002t0002g0048a0008c0013t0002g0033 | 2 | HG02074.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.646-1623_646-1622i others(602): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | |||||
| chr16:89852655
|
G | GATCCCAT others(753): Show |
1 | a0002c0002t0002g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.646-1623_646-1622i others(762): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | |||||
| chr16:89852655
|
G | GATCCCAT others(830): Show |
1 | a0002c0002t0002g0038 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.646-1623_646-1622i others(839): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | |||||
| chr16:89852655
|
G | GATCCCAT others(633): Show |
1 | a0002c0002t0002g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.646-1623_646-1622i others(642): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | |||||
| chr16:89852655
|
G | GATCCCAT others(634): Show |
1 | a0002c0002t0002g0029 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.646-1623_646-1622i others(643): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | |||||
| chr16:89852655
|
G | GATCCCAT others(633): Show |
11 | a0002c0002t0002g0022a0002c0002t0002g0028a0002c0002t0002g0034others(8): Show | 11 | HG00438.hp2 HG00621.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.646-1623_646-1622i others(642): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | |||||
| chr16:89852655
|
G | GATCCCAT others(673): Show |
1 | a0009c0025t0002g0039 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.646-1623_646-1622i others(682): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | |||||
| chr16:89852655
|
G | GATCCCAT others(673): Show |
1 | a0002c0002t0002g0035 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.646-1623_646-1622i others(682): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852655 | |||||
| chr16:89852661
|
A | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0077a0001c0001t0001g0081others(3): Show | 6 | HG00741.hp2 HG01074.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-1625A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852661 | ||||||
| chr16:89852664
|
G | A | 6 | a0001c0001t0001g0134a0001c0001t0001g0150a0001c0001t0001g0210others(3): Show | 6 | HG01106.hp2 HG02622.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1622G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852664 | ||||||
| chr16:89852665
|
C | T | 6 | a0001c0001t0001g0134a0001c0001t0001g0150a0001c0001t0001g0210others(3): Show | 6 | HG01106.hp2 HG02622.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1621C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852665 | ||||||
| chr16:89852665
|
CCCGTCAT others(33): Show |
C | 8 | a0001c0001t0001g0099a0001c0001t0001g0125a0001c0001t0001g0160others(5): Show | 8 | HG00408.hp2 HG00741.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.646-1615_646-1576d others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852665 | |||||
| chr16:89852668
|
G | A | 8 | a0001c0001t0001g0060a0001c0001t0001g0134a0001c0001t0001g0150others(5): Show | 8 | HG01106.hp2 HG01261.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.646-1618G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852668 | ||||||
| chr16:89852671
|
A | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0077others(221): Show | 224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.646-1615A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852671 | ||||||
| chr16:89852673
|
C | A | 7 | a0002c0002t0002g0024a0002c0002t0002g0025a0002c0002t0002g0031others(4): Show | 7 | HG02015.hp1 HG02080.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.646-1613C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852673 | ||||||
| chr16:89852675
|
G | A | 7 | a0001c0001t0001g0083a0001c0001t0001g0134a0001c0001t0001g0150others(4): Show | 7 | HG01106.hp2 HG02622.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.646-1611G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852675 | ||||||
| chr16:89852678
|
T | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0077others(192): Show | 195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.646-1608T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852678 | ||||||
| chr16:89852681
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0081others(190): Show | 193 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.646-1605T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852681 | ||||||
| chr16:89852683
|
T | C | 2 | a0001c0001t0001g0060a0001c0009t0001g0018 | 2 | HG01261.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.646-1603T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852683 | ||||||
| chr16:89852684
|
C | CCACCCCC others(31): Show |
1 | a0001c0001t0001g0060 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.646-1602_646-1601i others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852684 | ||||||
| chr16:89852685
|
T | C | 2 | a0001c0001t0001g0060a0001c0009t0001g0018 | 2 | HG01261.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.646-1601T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852685 | ||||||
| chr16:89852694
|
G | A | 7 | a0001c0001t0001g0060a0001c0001t0001g0181a0001c0001t0001g0219others(4): Show | 7 | HG00621.hp2 HG01256.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.646-1592G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852694 | ||||||
| chr16:89852694
|
G | C | 1 | a0001c0006t0001g0012 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.646-1592G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852694 | ||||||
| chr16:89852695
|
G | C | 49 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0091others(46): Show | 49 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.646-1591G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852695 | ||||||
| chr16:89852695
|
G | T | 1 | a0001c0009t0001g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.646-1591G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852695 | ||||||
| chr16:89852696
|
A | C | 1 | a0001c0006t0001g0012 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.646-1590A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852696 | ||||||
| chr16:89852697
|
T | A | 1 | a0001c0006t0001g0012 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.646-1589T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852697 | ||||||
| chr16:89852698
|
C | T | 2 | a0001c0006t0001g0012a0001c0009t0001g0018 | 2 | HG03669.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.646-1588C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852698 | ||||||
| chr16:89852701
|
A | C | 1 | a0001c0001t0001g0060 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.646-1585A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852701 | ||||||
| chr16:89852703
|
G | GGCCCGTC others(230): Show |
2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.646-1583_646-1582i others(239): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852703 | ||||||
| chr16:89852703
|
G | GGCCCGTC others(270): Show |
1 | a0001c0001t0001g0177 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.646-1583_646-1582i others(279): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852703 | ||||||
| chr16:89852703
|
G | GGCCCGTC others(310): Show |
1 | a0001c0001t0001g0151 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.646-1583_646-1582i others(319): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852703 | ||||||
| chr16:89852703
|
G | GGCCCGTC others(110): Show |
1 | a0001c0001t0001g0079 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.646-1583_646-1582i others(119): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852703 | ||||||
| chr16:89852704
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0062others(190): Show | 193 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.646-1582A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852704 | ||||||
| chr16:89852705
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0062others(190): Show | 193 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.646-1581T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852705 | ||||||
| chr16:89852705
|
T | TCCATCTT others(153): Show |
1 | a0001c0001t0001g0006 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(994): Show |
1 | a0001c0001t0001g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1003): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(33): Show |
19 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0001t0001g0087others(16): Show | 19 | HG00597.hp1 HG00733.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.646-1579_646-1578i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(553): Show |
1 | a0001c0001t0001g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(562): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(74): Show |
1 | a0001c0001t0001g0213 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(83): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(73): Show |
6 | a0001c0001t0001g0104a0001c0001t0001g0159a0001c0001t0001g0289others(3): Show | 6 | HG01109.hp1 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-1579_646-1578i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(313): Show |
1 | a0001c0001t0001g0350 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(322): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(711): Show |
1 | a0001c0027t0001g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(720): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(153): Show |
1 | a0001c0001t0001g0253 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(113): Show |
4 | a0003c0005t0001g0309a0003c0005t0001g0310a0003c0005t0001g0311others(1): Show | 4 | HG02602.hp1 HG03688.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1579_646-1578i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(233): Show |
1 | a0001c0001t0001g0117 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(274): Show |
1 | a0001c0001t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(283): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(153): Show |
1 | a0001c0001t0001g0209 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(193): Show |
1 | a0001c0001t0001g0176 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(473): Show |
1 | a0001c0001t0001g0264 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(482): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(353): Show |
1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(433): Show |
1 | a0001c0001t0001g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(442): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(473): Show |
1 | a0001c0003t0001g0120 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(482): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(73): Show |
1 | a0003c0005t0001g0299 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(393): Show |
1 | a0001c0001t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(402): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(353): Show |
1 | a0001c0001t0003g0320 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(1434): Show |
1 | a0001c0001t0003g0331 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1443): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(1313): Show |
2 | a0001c0001t0003g0323a0001c0001t0003g0338 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.646-1579_646-1578i others(1322): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(1793): Show |
1 | a0001c0001t0003g0344 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1802): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(1153): Show |
1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(1313): Show |
1 | a0001c0001t0003g0341 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1322): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(1953): Show |
1 | a0001c0001t0003g0342 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1962): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(1193): Show |
2 | a0001c0001t0003g0330a0001c0001t0003g0339 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.646-1579_646-1578i others(1202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(953): Show |
1 | a0001c0001t0003g0343 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(962): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(1233): Show |
1 | a0001c0001t0003g0340 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(393): Show |
1 | a0002c0002t0002g0045 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(402): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(433): Show |
1 | a0005c0007t0002g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(442): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(273): Show |
1 | a0001c0001t0004g0316 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(282): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(993): Show |
1 | a0001c0001t0001g0154 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1002): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(1073): Show |
3 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0157 | 3 | HG02109.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.646-1579_646-1578i others(1082): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(913): Show |
1 | a0001c0001t0001g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(922): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(1073): Show |
1 | a0001c0001t0001g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1082): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(1073): Show |
1 | a0001c0001t0001g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(1082): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCATCTT others(233): Show |
1 | a0001c0001t0001g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.646-1579_646-1578i others(242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCGTCTT others(33): Show |
1 | a0001c0001t0001g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.646-1471_646-1432d others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCGTCTT others(73): Show |
1 | a0001c0001t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.646-1511_646-1432d others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TCCGTCTT others(113): Show |
1 | a0001c0001t0001g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.646-1551_646-1432d others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
T | TGGC | 5 | a0001c0001t0001g0079a0001c0001t0001g0151a0001c0001t0001g0177others(2): Show | 5 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-1581_646-1580i others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852705 | ||||||
| chr16:89852705
|
TCCGTCTT others(33): Show |
T | 3 | a0001c0001t0001g0112a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.646-1471_646-1432d others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852705
|
TCCGTCTT others(73): Show |
T | 1 | a0001c0001t0001g0242 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.646-1511_646-1432d others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852705 | |||||
| chr16:89852708
|
G | A | 21 | a0001c0001t0001g0126a0001c0001t0001g0149a0001c0001t0001g0161others(18): Show | 21 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.646-1578G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852708 | ||||||
| chr16:89852711
|
T | A | 8 | a0001c0001t0001g0077a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 8 | HG00741.hp2 HG01074.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.646-1575T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852711 | ||||||
| chr16:89852714
|
C | T | 23 | a0001c0001t0001g0254a0002c0002t0002g0022a0002c0002t0002g0023others(20): Show | 23 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.646-1572C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852714 | ||||||
| chr16:89852715
|
G | A | 20 | a0001c0001t0001g0083a0001c0001t0001g0126a0001c0001t0001g0149others(17): Show | 20 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.646-1571G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852715 | ||||||
| chr16:89852718
|
C | T | 6 | a0001c0001t0001g0077a0001c0001t0001g0081a0001c0001t0001g0082others(3): Show | 6 | HG00741.hp2 HG01074.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-1568C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852718 | ||||||
| chr16:89852721
|
C | T | 6 | a0001c0001t0001g0077a0001c0001t0001g0081a0001c0001t0001g0082others(3): Show | 6 | HG00741.hp2 HG01074.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-1565C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852721 | ||||||
| chr16:89852734
|
G | A | 21 | a0001c0001t0001g0099a0001c0001t0001g0117a0001c0001t0001g0130others(18): Show | 21 | HG00408.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.646-1552G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852734 | ||||||
| chr16:89852735
|
G | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0001g0057others(156): Show | 159 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.646-1551G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852735 | ||||||
| chr16:89852735
|
G | GATCCCAT others(152): Show |
1 | a0001c0001t0001g0265 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.646-1512_646-1511i others(161): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852735 | |||||
| chr16:89852735
|
G | GATCCCAT others(353): Show |
2 | a0002c0002t0002g0025a0002c0002t0002g0050 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.646-1474_646-1473i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852735 | |||||
| chr16:89852735
|
G | GATCCCAT others(473): Show |
1 | a0002c0002t0002g0031 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.646-1474_646-1473i others(482): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852735 | |||||
| chr16:89852741
|
A | ATGGCCCA others(32): Show |
1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.646-1539_646-1538i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852741 | |||||
| chr16:89852744
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0135a0006c0010t0008g0313 | 3 | HG01074.hp1 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.646-1542G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852744 | ||||||
| chr16:89852745
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0135a0006c0010t0008g0313 | 3 | HG01074.hp1 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.646-1541C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852745 | ||||||
| chr16:89852748
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.646-1538G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852748 | ||||||
| chr16:89852748
|
G | GTCTTCCG others(153): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0086 | 2 | HG00140.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.646-1419_646-1418i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852748 | |||||
| chr16:89852748
|
GTCTTCCG others(113): Show |
G | 1 | a0001c0001t0001g0149 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.646-1471_646-1352d others(2): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852748 | |||||
| chr16:89852751
|
T | A | 2 | a0001c0001t0001g0060a0001c0001t0002g0051 | 2 | HG00673.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.646-1535T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852751 | ||||||
| chr16:89852755
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.646-1531G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852755 | ||||||
| chr16:89852758
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0352a0004c0004t0001g0196 | 3 | HG01261.hp1 HG02293.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.646-1528C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852758 | ||||||
| chr16:89852761
|
C | CCTCTCAC others(33): Show |
1 | a0001c0001t0001g0254 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.646-1516_646-1515i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852761 | |||||
| chr16:89852761
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0352a0004c0004t0001g0196 | 3 | HG01261.hp1 HG02293.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.646-1525C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852761 | ||||||
| chr16:89852774
|
G | A | 16 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0071others(13): Show | 16 | HG00099.hp2 HG00621.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.646-1512G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852774 | ||||||
| chr16:89852775
|
G | C | 70 | a0001c0001t0001g0054a0001c0001t0001g0084a0001c0001t0001g0100others(67): Show | 70 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.646-1511G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852775 | ||||||
| chr16:89852775
|
G | GATCCCAT others(591): Show |
1 | a0001c0001t0001g0354 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.646-1489_646-1488i others(600): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852775 | |||||
| chr16:89852784
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0352 | 2 | HG01261.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.646-1502G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852784 | ||||||
| chr16:89852785
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0352 | 2 | HG01261.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.646-1501C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852785 | ||||||
| chr16:89852788
|
G | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0352 | 2 | HG02293.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.646-1498G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852788 | ||||||
| chr16:89852788
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.646-1498G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852788 | ||||||
| chr16:89852788
|
GTCTTCCG others(73): Show |
G | 4 | a0001c0001t0001g0099a0001c0001t0001g0191a0001c0001t0001g0203others(1): Show | 4 | HG00408.hp2 NA19005.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-1418_646-1339d others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852788 | |||||
| chr16:89852791
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.646-1495T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852791 | ||||||
| chr16:89852794
|
C | CGTCCTCC others(353): Show |
1 | a0002c0002t0002g0024 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.646-1474_646-1473i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852794 | |||||
| chr16:89852795
|
G | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0352a0006c0010t0001g0314 | 3 | HG02293.hp2 HG03017.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.646-1491G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852795 | ||||||
| chr16:89852798
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0353 | 2 | HG01192.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.646-1488C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852798 | ||||||
| chr16:89852801
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0353 | 2 | HG01192.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.646-1485C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852801 | ||||||
| chr16:89852814
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0115others(72): Show | 75 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.646-1472G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852814 | ||||||
| chr16:89852814
|
G | GCATCCCA others(73): Show |
1 | a0001c0001t0001g0213 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.646-1472_646-1471i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852814 | ||||||
| chr16:89852814
|
G | GCATCCCA others(273): Show |
1 | a0001c0001t0001g0349 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.646-1472_646-1471i others(282): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852814 | ||||||
| chr16:89852814
|
G | GCATCCCA others(193): Show |
1 | a0012c0017t0001g0148 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.646-1472_646-1471i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852814 | ||||||
| chr16:89852814
|
G | GGATCCCA others(553): Show |
1 | a0001c0001t0001g0353 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.646-1463_646-1462i others(562): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852814 | |||||
| chr16:89852815
|
G | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0062others(61): Show | 64 | HG00597.hp1 HG00733.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.646-1471G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852815 | ||||||
| chr16:89852821
|
A | C | 1 | a0001c0001t0001g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.646-1465A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852821 | ||||||
| chr16:89852824
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0003g0320 | 2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.646-1462G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852824 | ||||||
| chr16:89852825
|
C | CCCGTCTT others(33): Show |
1 | a0002c0002t0002g0037 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.646-1451_646-1450i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852825 | |||||
| chr16:89852825
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0003g0320 | 2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.646-1461C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852825 | ||||||
| chr16:89852828
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.646-1458G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852828 | ||||||
| chr16:89852828
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.646-1458G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852828 | ||||||
| chr16:89852828
|
GTCTTCCG others(33): Show |
G | 1 | a0001c0001t0001g0126 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.646-1431_646-1392d others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852828 | |||||
| chr16:89852835
|
G | A | 3 | a0001c0001t0001g0123a0001c0019t0001g0317a0006c0010t0001g0314 | 3 | HG03139.hp1 NA19007.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.646-1451G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852835 | ||||||
| chr16:89852837
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.646-1449C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852837 | ||||||
| chr16:89852847
|
A | ACCCCCCG others(314): Show |
1 | a0001c0006t0001g0016 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.646-1432_646-1431i others(323): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852847 | |||||
| chr16:89852851
|
C | T | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.646-1435C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852851 | ||||||
| chr16:89852853
|
C | A | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.646-1433C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852853 | ||||||
| chr16:89852853
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.646-1433C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852853 | ||||||
| chr16:89852854
|
G | A | 31 | a0001c0001t0001g0054a0001c0001t0001g0100a0001c0001t0001g0105others(28): Show | 31 | HG00280.hp1 HG00621.hp2 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.646-1432G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852854 | ||||||
| chr16:89852854
|
G | GGATCCCA others(33): Show |
1 | a0001c0001t0001g0091 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.646-1432_646-1431i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852854 | ||||||
| chr16:89852854
|
G | GGATCCCA others(153): Show |
1 | a0001c0001t0001g0184 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.646-1432_646-1431i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852854 | ||||||
| chr16:89852855
|
C | CATCCCAT others(353): Show |
1 | a0001c0001t0001g0347 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.646-1419_646-1418i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852855 | |||||
| chr16:89852855
|
C | CATCCCAT others(33): Show |
1 | a0001c0001t0002g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.646-1419_646-1418i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852855 | |||||
| chr16:89852855
|
C | CATCCCAT others(473): Show |
1 | a0010c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.646-1419_646-1418i others(482): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852855 | |||||
| chr16:89852855
|
C | CATCCCAT others(33): Show |
1 | a0001c0001t0001g0352 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.646-1419_646-1418i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852855 | |||||
| chr16:89852855
|
C | CATCCCAT others(73): Show |
7 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0267others(4): Show | 7 | HG00597.hp1 HG01106.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.646-1419_646-1418i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852855 | |||||
| chr16:89852855
|
C | CATCCCAT others(113): Show |
11 | a0001c0001t0001g0190a0001c0001t0001g0210a0001c0001t0001g0221others(8): Show | 11 | HG01168.hp2 HG01169.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.646-1419_646-1418i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852855 | |||||
| chr16:89852855
|
C | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(182): Show | 185 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.646-1431C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852855 | ||||||
| chr16:89852861
|
A | ATGGCCCG others(33): Show |
5 | a0001c0001t0001g0289a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG01109.hp1 HG01123.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-1419_646-1418i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852861 | |||||
| chr16:89852861
|
A | ATGGCCCG others(193): Show |
1 | a0001c0001t0001g0290 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.646-1419_646-1418i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852861 | |||||
| chr16:89852861
|
A | ATGGCCCG others(753): Show |
1 | a0001c0001t0001g0327 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.646-1419_646-1418i others(762): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852861 | |||||
| chr16:89852861
|
A | C | 1 | a0001c0001t0001g0288 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.646-1425A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852861 | ||||||
| chr16:89852868
|
C | A | 9 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(6): Show | 9 | HG01109.hp1 HG01123.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-1418C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852868 | ||||||
| chr16:89852868
|
C | CTCTTCCG others(113): Show |
6 | a0001c0001t0001g0279a0001c0001t0001g0282a0001c0001t0001g0283others(3): Show | 6 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-1332_646-1331i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852868 | |||||
| chr16:89852868
|
C | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.646-1418C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852868 | ||||||
| chr16:89852868
|
C | TTCTTCCG others(113): Show |
2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.646-1418delCinsTTC others(118): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852868 | ||||||
| chr16:89852875
|
G | A | 1 | a0001c0001t0003g0320 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.646-1411G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852875 | ||||||
| chr16:89852875
|
G | GTCCTCCC others(193): Show |
1 | a0011c0022t0001g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.646-1396_646-1395i others(202): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852875 | |||||
| chr16:89852891
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0219 | 2 | HG03209.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.646-1395C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852891 | ||||||
| chr16:89852893
|
C | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0219 | 2 | HG03209.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.646-1393C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852893 | ||||||
| chr16:89852893
|
C | CAGATCCC others(33): Show |
4 | a0001c0003t0001g0127a0001c0003t0001g0132a0001c0003t0001g0133others(1): Show | 4 | HG01928.hp2 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1393_646-1392i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852893 | ||||||
| chr16:89852894
|
G | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0219a0001c0001t0001g0233 | 3 | HG03209.hp2 HG04199.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.646-1392G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852894 | ||||||
| chr16:89852895
|
G | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0062a0001c0001t0001g0083others(48): Show | 51 | HG00099.hp1 HG00741.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.646-1391G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852895 | ||||||
| chr16:89852895
|
G | GATCCCAT others(113): Show |
3 | a0001c0001t0001g0057a0001c0001t0001g0104a0001c0001t0001g0159 | 3 | HG02698.hp2 HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.646-1353_646-1352i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | |||||
| chr16:89852895
|
G | GATCCCAT others(153): Show |
2 | a0001c0006t0001g0007a0001c0006t0001g0015 | 2 | HG03490.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.646-1353_646-1352i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | |||||
| chr16:89852895
|
G | GATCCCAT others(33): Show |
2 | a0001c0001t0001g0068a0001c0001t0001g0087 | 2 | HG00733.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.646-1371_646-1332d others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | |||||
| chr16:89852895
|
G | GATCCCAT others(73): Show |
1 | a0001c0001t0001g0119 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.646-1352_646-1351i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | |||||
| chr16:89852895
|
G | GATCCCAT others(313): Show |
2 | a0003c0005t0001g0296a0003c0005t0001g0298 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.646-1352_646-1351i others(322): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | |||||
| chr16:89852895
|
G | GATCCCAT others(113): Show |
1 | a0001c0001t0001g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.646-1352_646-1351i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | |||||
| chr16:89852895
|
G | GATCCCAT others(313): Show |
1 | a0001c0001t0001g0236 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.646-1356_646-1355i others(322): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852895 | |||||
| chr16:89852908
|
G | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0083 | 2 | HG01074.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.646-1378G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852908 | ||||||
| chr16:89852908
|
G | GTCTTCCA others(33): Show |
1 | a0001c0001t0001g0079 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.646-1372_646-1371i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852908 | |||||
| chr16:89852908
|
G | GTCTTCCA others(353): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0085 | 3 | HG01123.hp1 HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.646-1372_646-1371i others(362): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852908 | |||||
| chr16:89852908
|
G | GTCTTCCA others(273): Show |
1 | a0001c0001t0001g0063 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.646-1372_646-1371i others(282): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852908 | |||||
| chr16:89852915
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0292a0003c0005t0001g0300 | 3 | HG00099.hp1 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.646-1371G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852915 | ||||||
| chr16:89852915
|
G | GTCCTCCC others(713): Show |
1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.646-1352_646-1351i others(722): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852915 | |||||
| chr16:89852921
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.646-1365C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852921 | ||||||
| chr16:89852931
|
C | T | 2 | a0001c0001t0001g0185a0011c0022t0001g0255 | 2 | HG01928.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.646-1355C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852931 | ||||||
| chr16:89852933
|
C | A | 2 | a0001c0001t0001g0185a0011c0022t0001g0255 | 2 | HG01928.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.646-1353C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852933 | ||||||
| chr16:89852934
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0247a0011c0022t0001g0255 | 3 | HG01928.hp1 NA19067.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.646-1352G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852934 | ||||||
| chr16:89852934
|
G | GGATCCCA others(313): Show |
1 | a0001c0001t0001g0222 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.646-1352_646-1351i others(322): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852934 | ||||||
| chr16:89852935
|
C | CATCCCAT others(113): Show |
1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.646-1332_646-1331i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852935 | |||||
| chr16:89852935
|
C | CATCCCAT others(33): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0147 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.646-1332_646-1331i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852935 | |||||
| chr16:89852935
|
C | CATCCCAT others(73): Show |
1 | a0001c0001t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.646-1332_646-1331i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852935 | |||||
| chr16:89852935
|
C | CATCCCAT others(233): Show |
1 | a0002c0002t0002g0037 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.646-1333_646-1332i others(242): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852935 | |||||
| chr16:89852935
|
C | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 174 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.646-1351C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852935 | ||||||
| chr16:89852944
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.646-1342G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852944 | ||||||
| chr16:89852948
|
G | GTCTTCCG others(153): Show |
2 | a0001c0001t0001g0231a0001c0001t0001g0245 | 2 | NA18949.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.646-1332_646-1331i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852948 | |||||
| chr16:89852948
|
G | GTCTTCCG others(73): Show |
1 | a0001c0001t0002g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.646-1332_646-1331i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852948 | |||||
| chr16:89852955
|
A | ATCCTCCC others(33): Show |
18 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(15): Show | 18 | HG00735.hp2 HG01109.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.646-1312_646-1311i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852955 | |||||
| chr16:89852955
|
A | ATCCTCCC others(113): Show |
1 | a0001c0018t0012g0346 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.646-1312_646-1311i others(122): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852955 | |||||
| chr16:89852955
|
A | ATCCTCCC others(153): Show |
1 | a0001c0001t0010g0348 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.646-1312_646-1311i others(162): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852955 | |||||
| chr16:89852955
|
A | ATCCTCCC others(73): Show |
1 | a0001c0001t0001g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.646-1292_646-1291i others(82): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852955 | |||||
| chr16:89852955
|
A | ATCCTCCC others(1673): Show |
1 | a0001c0001t0003g0336 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.646-1316_646-1315i others(1682): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852955 | |||||
| chr16:89852955
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(269): Show | 272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.646-1331A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852955 | ||||||
| chr16:89852967
|
A | ACCCCCCG others(118): Show |
1 | a0001c0001t0001g0247 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.646-1307_646-1306i others(127): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852967 | |||||
| chr16:89852971
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0264 | 2 | HG01256.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.646-1315C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852971 | ||||||
| chr16:89852973
|
C | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0264 | 2 | HG01256.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.646-1313C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852973 | ||||||
| chr16:89852974
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0264a0015c0023t0001g0055 | 3 | HG01256.hp2 HG01346.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.646-1312G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852974 | ||||||
| chr16:89852974
|
GGATCCCA others(33): Show |
G | 1 | a0013c0020t0001g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.646-1298_646-1259d others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89852974 | |||||
| chr16:89852975
|
G | C | 1 | a0001c0001t0003g0326 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.646-1311G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852975 | ||||||
| chr16:89852995
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 258 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.646-1291A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89852995 | ||||||
| chr16:89853028
|
A | G | 3 | a0001c0001t0001g0161a0001c0001t0001g0218a0001c0001t0001g0267 | 3 | HG00673.hp2 HG01192.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.646-1258A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853028 | ||||||
| chr16:89853081
|
C | T | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.646-1205C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853081 | ||||||
| chr16:89853310
|
ACTTT | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(242): Show | 245 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.646-971_646-968del others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 89853310 | |||||
| chr16:89853476
|
C | T | 12 | a0001c0001t0003g0320a0001c0001t0003g0323a0001c0001t0003g0330others(9): Show | 12 | HG01192.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.646-810C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853476 | ||||||
| chr16:89853602
|
C | T | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.646-684C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853602 | ||||||
| chr16:89853617
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(235): Show | 238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.646-669C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853617 | ||||||
| chr16:89853679
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.646-607C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853679 | ||||||
| chr16:89853705
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.646-581G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853705 | ||||||
| chr16:89853738
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.646-548G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853738 | ||||||
| chr16:89853794
|
G | A | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.646-492G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853794 | ||||||
| chr16:89853911
|
C | T | 8 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(5): Show | 8 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.646-375C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853911 | ||||||
| chr16:89853975
|
C | A | 33 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.646-311C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853975 | ||||||
| chr16:89853991
|
C | A | 3 | a0001c0009t0001g0017a0001c0009t0001g0018a0001c0009t0001g0019 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.646-295C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89853991 | ||||||
| chr16:89854089
|
C | T | 40 | a0001c0001t0001g0091a0001c0001t0001g0105a0001c0001t0001g0106others(37): Show | 40 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.646-197C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89854089 | ||||||
| chr16:89854105
|
T | G | 1 | a0001c0001t0003g0334 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.646-181T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89854105 | ||||||
| chr16:89854195
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.646-91C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 3/14 | chr16 | 89854195 | ||||||
| chr16:89854405
|
C | T | 1 | a0004c0004t0001g0205 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.726+39C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 4/14 | chr16 | 89854405 | ||||||
| chr16:89854649
|
A | ATGGTGAG others(39): Show |
1 | a0016c0015t0002g0049 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.891+12_891+57dupAG others(44): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854649 | |||||
| chr16:89854649
|
A | ATGGTGAG others(85): Show |
1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.891+57_891+58insAG others(90): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854649 | |||||
| chr16:89854649
|
A | ATGGTGAG others(85): Show |
26 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0024others(23): Show | 26 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.891+59_891+60insCC others(90): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854649 | |||||
| chr16:89854663
|
A | G | 2 | a0001c0019t0001g0317a0006c0010t0001g0314 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.891+12A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854663 | ||||||
| chr16:89854665
|
A | ACGCAGAG others(39): Show |
2 | a0005c0007t0002g0041a0005c0014t0002g0021 | 2 | HG00621.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.891+59_891+60insCC others(44): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854665 | |||||
| chr16:89854665
|
A | C | 2 | a0001c0019t0001g0317a0006c0010t0001g0314 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.891+14A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854665 | ||||||
| chr16:89854670
|
GA | G | 3 | a0001c0009t0001g0017a0001c0009t0001g0018a0001c0009t0001g0019 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.891+20delA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854670 | ||||||
| chr16:89854674
|
GGCAGCCT others(39): Show |
G | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.891+36_891+81delCA others(44): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854674 | |||||
| chr16:89854695
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.891+44G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854695 | ||||||
| chr16:89854709
|
G | A | 5 | a0001c0001t0001g0189a0001c0001t0001g0215a0001c0009t0001g0017others(2): Show | 5 | HG03669.hp2 HG04115.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+58G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854709 | ||||||
| chr16:89854711
|
A | ACGCAGAG others(85): Show |
1 | a0001c0001t0001g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.891+66_891+67insGG others(90): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854711 | |||||
| chr16:89854711
|
A | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0063others(53): Show | 56 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.891+60A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854711 | ||||||
| chr16:89854718
|
T | G | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0058others(56): Show | 59 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.891+67T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854718 | ||||||
| chr16:89854720
|
A | G | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0058others(56): Show | 59 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.891+69A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854720 | ||||||
| chr16:89854735
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.891+84G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89854735 | ||||||
| chr16:89854939
|
A | AT | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(242): Show | 245 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.891+298dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr16 | 89854939 | |||||
| chr16:89855001
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.891+350C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855001 | ||||||
| chr16:89855004
|
C | T | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.891+353C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855004 | ||||||
| chr16:89855042
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.891+391G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855042 | ||||||
| chr16:89855123
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.891+472A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855123 | ||||||
| chr16:89855150
|
C | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0076 | 2 | HG01074.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.892-450C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855150 | ||||||
| chr16:89855180
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.892-420T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855180 | ||||||
| chr16:89855185
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.892-415A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855185 | ||||||
| chr16:89855222
|
G | A | 1 | a0001c0001t0003g0343 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.892-378G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855222 | ||||||
| chr16:89855257
|
C | G | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.892-343C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855257 | ||||||
| chr16:89855387
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.892-213C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855387 | ||||||
| chr16:89855412
|
C | A | 11 | a0001c0001t0003g0320a0001c0001t0003g0323a0001c0001t0003g0330others(8): Show | 11 | HG01192.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.892-188C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855412 | ||||||
| chr16:89855585
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.892-15C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 5/14 | chr16 | 89855585 | ||||||
| chr16:89855810
|
C | T | 1 | a0001c0018t0012g0346 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.978+124C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89855810 | ||||||
| chr16:89855824
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.978+138C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89855824 | ||||||
| chr16:89855856
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0207a0001c0001t0004g0244 | 3 | NA18974.hp1 NA18974.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.978+170C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89855856 | ||||||
| chr16:89855973
|
G | T | 2 | a0003c0005t0001g0296a0003c0005t0001g0298 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.979-140G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89855973 | ||||||
| chr16:89855990
|
G | A | 2 | a0001c0001t0001g0321a0001c0001t0001g0322 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.979-123G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89855990 | ||||||
| chr16:89856018
|
A | G | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.979-95A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89856018 | ||||||
| chr16:89856057
|
CGCTTCCC others(13): Show |
C | 3 | a0001c0001t0001g0190a0001c0019t0001g0317a0006c0010t0001g0314 | 3 | HG03139.hp1 NA18954.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.979-37_979-18delCT others(18): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 89856057 | |||||
| chr16:89856077
|
T | C | 40 | a0001c0001t0001g0347a0001c0001t0001g0349a0001c0001t0001g0351others(37): Show | 40 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.979-36T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 6/14 | chr16 | 89856077 | ||||||
| chr16:89856319
|
A | C | 2 | a0001c0001t0001g0160a0012c0017t0001g0148 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1102+83A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856319 | ||||||
| chr16:89856327
|
G | A | 16 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0001t0001g0084others(13): Show | 16 | HG00733.hp2 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1102+91G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856327 | ||||||
| chr16:89856340
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1102+104C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856340 | ||||||
| chr16:89856459
|
G | C | 1 | a0001c0003t0001g0165 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1102+223G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856459 | ||||||
| chr16:89856508
|
G | A | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1102+272G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856508 | ||||||
| chr16:89856530
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1102+294C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856530 | ||||||
| chr16:89856538
|
G | A | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1102+302G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856538 | ||||||
| chr16:89856547
|
T | G | 1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1102+311T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856547 | ||||||
| chr16:89856551
|
G | T | 33 | a0001c0001t0002g0122a0002c0002t0002g0022a0002c0002t0002g0023others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1102+315G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856551 | ||||||
| chr16:89856611
|
AT | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0069others(15): Show | 18 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1102+395delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89856611 | |||||
| chr16:89856611
|
ATT | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(278): Show | 281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1102+394_1102+395d others(4): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89856611 | |||||
| chr16:89856611
|
ATTT | A | 13 | a0001c0001t0001g0104a0001c0001t0001g0124a0001c0001t0001g0125others(10): Show | 13 | HG02083.hp1 HG02083.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.1102+393_1102+395d others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89856611 | |||||
| chr16:89856718
|
C | T | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1102+482C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856718 | ||||||
| chr16:89856822
|
A | C | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1102+586A>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856822 | ||||||
| chr16:89856985
|
G | A | 2 | a0003c0005t0001g0311a0003c0005t0001g0312 | 2 | HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1102+749G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856985 | ||||||
| chr16:89856993
|
G | A | 3 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0018t0012g0346 | 3 | HG01243.hp1 HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1102+757G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89856993 | ||||||
| chr16:89857004
|
C | T | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(300): Show | 303 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1102+768C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857004 | ||||||
| chr16:89857065
|
C | CA | 44 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0089others(41): Show | 44 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1102+844dupA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89857065 | |||||
| chr16:89857136
|
C | CT | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0054others(233): Show | 236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1102+918dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89857136 | |||||
| chr16:89857136
|
CT | C | 28 | a0001c0001t0001g0064a0001c0001t0001g0071a0001c0001t0001g0328others(25): Show | 28 | HG00099.hp2 HG01081.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1102+918delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89857136 | |||||
| chr16:89857177
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0011t0001g0318others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102+941C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857177 | ||||||
| chr16:89857351
|
G | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(239): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1103-987G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857351 | ||||||
| chr16:89857396
|
G | A | 4 | a0001c0009t0001g0017a0001c0009t0001g0018a0001c0009t0001g0019others(1): Show | 4 | HG02451.hp2 HG03669.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-942G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857396 | ||||||
| chr16:89857427
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1103-911T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857427 | ||||||
| chr16:89857498
|
C | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(266): Show | 269 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1103-840C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857498 | ||||||
| chr16:89857552
|
T | A | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1103-786T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857552 | ||||||
| chr16:89857558
|
G | C | 1 | a0001c0001t0001g0182 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1103-780G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857558 | ||||||
| chr16:89857601
|
G | A | 1 | a0001c0001t0003g0325 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1103-737G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857601 | ||||||
| chr16:89857603
|
C | T | 1 | a0001c0027t0001g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1103-735C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857603 | ||||||
| chr16:89857609
|
T | G | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1103-729T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857609 | ||||||
| chr16:89857620
|
G | T | 1 | a0001c0001t0003g0332 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1103-718G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857620 | ||||||
| chr16:89857624
|
G | A | 2 | a0001c0003t0001g0102a0001c0003t0001g0103 | 2 | NA18970.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1103-714G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857624 | ||||||
| chr16:89857714
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(240): Show | 243 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1103-624G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857714 | ||||||
| chr16:89857720
|
G | A | 1 | a0004c0004t0001g0195 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1103-618G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857720 | ||||||
| chr16:89857793
|
C | T | 1 | a0001c0021t0001g0065 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1103-545C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857793 | ||||||
| chr16:89857849
|
C | T | 4 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0087others(1): Show | 4 | HG00733.hp2 HG01071.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-489C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857849 | ||||||
| chr16:89857850
|
G | A | 3 | a0001c0009t0001g0017a0001c0009t0001g0018a0001c0009t0001g0019 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1103-488G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857850 | ||||||
| chr16:89857881
|
C | CT | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(213): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1103-438dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89857881 | |||||
| chr16:89857881
|
CT | C | 7 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0074others(4): Show | 7 | HG00099.hp2 HG01070.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1103-438delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 89857881 | |||||
| chr16:89857883
|
T | TC | 16 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0142others(13): Show | 16 | HG00099.hp1 HG00735.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1103-455_1103-454i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857883 | ||||||
| chr16:89857884
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0137 | 2 | HG01074.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1103-454T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857884 | ||||||
| chr16:89857916
|
T | C | 3 | a0001c0009t0001g0017a0001c0009t0001g0018a0001c0009t0001g0019 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1103-422T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857916 | ||||||
| chr16:89857951
|
C | T | 1 | a0001c0001t0001g0002 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1103-387C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857951 | ||||||
| chr16:89857994
|
T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(268): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1103-344T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89857994 | ||||||
| chr16:89858007
|
C | T | 13 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0087others(10): Show | 13 | HG00733.hp2 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1103-331C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858007 | ||||||
| chr16:89858038
|
A | G | 20 | a0001c0001t0001g0104a0001c0001t0001g0131a0001c0001t0001g0135others(17): Show | 20 | HG01891.hp2 HG02145.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1103-300A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858038 | ||||||
| chr16:89858121
|
G | A | 21 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(18): Show | 21 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1103-217G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858121 | ||||||
| chr16:89858128
|
A | G | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1103-210A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858128 | ||||||
| chr16:89858134
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1103-204C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858134 | ||||||
| chr16:89858136
|
T | C | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1103-202T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858136 | ||||||
| chr16:89858162
|
G | A | 2 | a0001c0011t0001g0318a0001c0011t0001g0319 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1103-176G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 7/14 | chr16 | 89858162 | ||||||
| chr16:89858542
|
G | A | 3 | a0001c0009t0001g0017a0001c0009t0001g0018a0001c0009t0001g0019 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1272+35G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/14 | chr16 | 89858542 | ||||||
| chr16:89858609
|
G | C | 3 | a0001c0009t0001g0017a0001c0009t0001g0018a0001c0009t0001g0019 | 3 | HG03669.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1272+102G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/14 | chr16 | 89858609 | ||||||
| chr16:89858711
|
C | T | 8 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(5): Show | 8 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+204C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/14 | chr16 | 89858711 | ||||||
| chr16:89858762
|
C | T | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1272+255C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/14 | chr16 | 89858762 | ||||||
| chr16:89858846
|
C | T | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1273-319C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/14 | chr16 | 89858846 | ||||||
| chr16:89859148
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(240): Show | 243 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1273-17G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 8/14 | chr16 | 89859148 | ||||||
| chr16:89859500
|
C | T | 1 | a0001c0003t0001g0277 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1462+146C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859500 | ||||||
| chr16:89859689
|
G | T | 1 | a0013c0020t0001g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1462+335G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859689 | ||||||
| chr16:89859697
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1462+343G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859697 | ||||||
| chr16:89859766
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1462+412G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859766 | ||||||
| chr16:89859785
|
G | A | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1462+431G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859785 | ||||||
| chr16:89859986
|
G | A | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1462+632G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859986 | ||||||
| chr16:89859995
|
G | C | 1 | a0003c0005t0001g0304 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1462+641G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89859995 | ||||||
| chr16:89860046
|
C | A | 1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1463-637C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860046 | ||||||
| chr16:89860110
|
T | G | 1 | a0004c0004t0001g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1463-573T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860110 | ||||||
| chr16:89860185
|
C | G | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1463-498C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860185 | ||||||
| chr16:89860214
|
C | T | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1463-469C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860214 | ||||||
| chr16:89860311
|
T | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0091others(146): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1463-372T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860311 | ||||||
| chr16:89860331
|
T | C | 1 | a0013c0020t0001g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1463-352T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860331 | ||||||
| chr16:89860365
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1463-318C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860365 | ||||||
| chr16:89860413
|
G | A | 14 | a0001c0001t0001g0001a0001c0001t0001g0328a0001c0001t0001g0337others(11): Show | 14 | HG01109.hp2 HG01192.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1463-270G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860413 | ||||||
| chr16:89860462
|
C | T | 34 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(31): Show | 34 | HG00099.hp1 HG00323.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.1463-221C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 9/14 | chr16 | 89860462 | ||||||
| chr16:89860810
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1575+15G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860810 | ||||||
| chr16:89860857
|
C | T | 34 | a0001c0001t0002g0051a0001c0001t0002g0122a0002c0002t0002g0022others(31): Show | 34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1575+62C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860857 | ||||||
| chr16:89860908
|
G | A | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1575+113G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860908 | ||||||
| chr16:89860917
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1575+122G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860917 | ||||||
| chr16:89860920
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0134 | 3 | HG02622.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1575+125C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860920 | ||||||
| chr16:89860926
|
G | C | 1 | a0001c0001t0001g0171 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1575+131G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860926 | ||||||
| chr16:89860926
|
G | T | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1575+131G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860926 | ||||||
| chr16:89860945
|
T | TC | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0091others(194): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1575+150_1575+151i others(3): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860945 | ||||||
| chr16:89860949
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0306a0001c0001t0001g0308 | 3 | HG01109.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1575+154G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860949 | ||||||
| chr16:89860974
|
G | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0324 | 2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1575+179G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89860974 | ||||||
| chr16:89861117
|
G | C | 1 | a0005c0007t0002g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1575+322G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861117 | ||||||
| chr16:89861387
|
G | A | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1575+592G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861387 | ||||||
| chr16:89861499
|
C | G | 1 | a0001c0001t0004g0316 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1575+704C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861499 | ||||||
| chr16:89861528
|
G | A | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1575+733G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861528 | ||||||
| chr16:89861595
|
CAAAT | C | 4 | a0001c0008t0001g0008a0001c0008t0001g0009a0001c0008t0001g0010others(1): Show | 4 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+802_1575+805d others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 89861595 | |||||
| chr16:89861705
|
C | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0147 | 3 | HG02622.hp1 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1575+910C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861705 | ||||||
| chr16:89861716
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1575+921C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861716 | ||||||
| chr16:89861730
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1575+935C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861730 | ||||||
| chr16:89861834
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1575+1039C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861834 | ||||||
| chr16:89861905
|
T | C | 1 | a0001c0001t0004g0212 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1575+1110T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89861905 | ||||||
| chr16:89862003
|
C | CT | 27 | a0001c0001t0001g0002a0001c0001t0001g0150a0001c0001t0001g0151others(24): Show | 27 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1575+1225dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 89862003 | |||||
| chr16:89862054
|
A | G | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1575+1259A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862054 | ||||||
| chr16:89862090
|
G | A | 33 | a0001c0001t0002g0051a0001c0001t0002g0122a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1575+1295G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862090 | ||||||
| chr16:89862104
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0091others(125): Show | 128 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1575+1309T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862104 | ||||||
| chr16:89862153
|
A | G | 1 | a0001c0008t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1576-1323A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862153 | ||||||
| chr16:89862158
|
C | A | 2 | a0004c0004t0001g0187a0004c0004t0001g0205 | 2 | NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1576-1318C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862158 | ||||||
| chr16:89862159
|
G | A | 1 | a0001c0008t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1576-1317G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862159 | ||||||
| chr16:89862161
|
A | G | 1 | a0001c0008t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1576-1315A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862161 | ||||||
| chr16:89862193
|
C | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0091others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1576-1283C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862193 | ||||||
| chr16:89862315
|
T | C | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1576-1161T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862315 | ||||||
| chr16:89862327
|
C | T | 1 | a0002c0002t0002g0047 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1576-1149C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862327 | ||||||
| chr16:89862374
|
GAC | G | 125 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0091others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1576-1098_1576-109 others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 89862374 | |||||
| chr16:89862446
|
G | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0091others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1576-1030G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862446 | ||||||
| chr16:89862610
|
C | G | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1576-866C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862610 | ||||||
| chr16:89862807
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1576-669C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89862807 | ||||||
| chr16:89863054
|
G | A | 1 | a0006c0010t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1576-422G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89863054 | ||||||
| chr16:89863168
|
A | G | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1576-308A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89863168 | ||||||
| chr16:89863173
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1576-303G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89863173 | ||||||
| chr16:89863321
|
GGATGGCT others(9): Show |
G | 1 | a0001c0001t0001g0119 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1576-139_1576-124d others(18): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 89863321 | |||||
| chr16:89863355
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0011t0001g0318others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-121G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89863355 | ||||||
| chr16:89863434
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1576-42G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89863434 | ||||||
| chr16:89863449
|
G | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0147 | 3 | HG02622.hp1 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1576-27G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 10/14 | chr16 | 89863449 | ||||||
| chr16:89863627
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1710+17G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 11/14 | chr16 | 89863627 | ||||||
| chr16:89863668
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1710+58G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 11/14 | chr16 | 89863668 | ||||||
| chr16:89863679
|
T | A | 56 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0002g0051others(53): Show | 56 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1710+69T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 11/14 | chr16 | 89863679 | ||||||
| chr16:89863721
|
G | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0091others(125): Show | 128 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1711-73G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 11/14 | chr16 | 89863721 | ||||||
| chr16:89863731
|
G | C | 23 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(20): Show | 23 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1711-63G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 11/14 | chr16 | 89863731 | ||||||
| chr16:89863734
|
C | T | 1 | a0001c0003t0001g0278 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1711-60C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 11/14 | chr16 | 89863734 | ||||||
| chr16:89863917
|
G | A | 21 | a0001c0001t0002g0051a0002c0002t0002g0022a0002c0002t0002g0027others(18): Show | 21 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1778+56G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89863917 | ||||||
| chr16:89864006
|
G | A | 33 | a0001c0001t0002g0051a0001c0001t0002g0122a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1778+145G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864006 | ||||||
| chr16:89864018
|
A | G | 56 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0002g0051others(53): Show | 56 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1778+157A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864018 | ||||||
| chr16:89864173
|
C | A | 1 | a0001c0019t0001g0317 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1778+312C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864173 | ||||||
| chr16:89864248
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0071others(193): Show | 196 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1778+387A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864248 | ||||||
| chr16:89864329
|
C | T | 1 | a0001c0001t0006g0070 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1778+468C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864329 | ||||||
| chr16:89864331
|
C | G | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1778+470C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864331 | ||||||
| chr16:89864332
|
C | T | 1 | a0010c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1778+471C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864332 | ||||||
| chr16:89864382
|
T | A | 1 | a0001c0003t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1778+521T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864382 | ||||||
| chr16:89864509
|
G | A | 1 | a0003c0005t0001g0304 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1778+648G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864509 | ||||||
| chr16:89864593
|
C | T | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1778+732C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864593 | ||||||
| chr16:89864599
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1778+738T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864599 | ||||||
| chr16:89864733
|
T | G | 1 | a0001c0003t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1778+872T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864733 | ||||||
| chr16:89864735
|
A | T | 1 | a0010c0016t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1778+874A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89864735 | ||||||
| chr16:89864831
|
TCAACAAA others(9): Show |
T | 1 | a0001c0001t0001g0002 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1778+973_1778+988d others(18): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89864831 | |||||
| chr16:89864995
|
CT | C | 32 | a0001c0001t0002g0051a0001c0001t0002g0122a0002c0002t0002g0022others(29): Show | 32 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1778+1141delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89864995 | |||||
| chr16:89865002
|
T | C | 1 | a0002c0002t0002g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1778+1141T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865002 | ||||||
| chr16:89865004
|
C | CT | 56 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0072others(53): Show | 56 | HG00280.hp1 HG00642.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1778+1163dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89865004 | |||||
| chr16:89865004
|
C | T | 1 | a0002c0002t0002g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1778+1143C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865004 | ||||||
| chr16:89865004
|
CT | C | 9 | a0001c0001t0001g0062a0001c0001t0001g0125a0001c0001t0001g0178others(6): Show | 9 | HG01070.hp2 HG01099.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1778+1163delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89865004 | |||||
| chr16:89865063
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG00735.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1778+1202G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865063 | ||||||
| chr16:89865069
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1778+1208C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865069 | ||||||
| chr16:89865078
|
C | G | 9 | a0001c0001t0001g0328a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1778+1217C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865078 | ||||||
| chr16:89865093
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1778+1232G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865093 | ||||||
| chr16:89865098
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1778+1237C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865098 | ||||||
| chr16:89865106
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1778+1245C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865106 | ||||||
| chr16:89865130
|
C | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0324 | 2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1778+1269C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865130 | ||||||
| chr16:89865357
|
G | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1778+1496G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865357 | ||||||
| chr16:89865566
|
C | G | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(325): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.1778+1705C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865566 | ||||||
| chr16:89865638
|
G | A | 8 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0252others(5): Show | 8 | HG00323.hp2 HG00733.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1778+1777G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865638 | ||||||
| chr16:89865735
|
A | G | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.1778+1874A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89865735 | ||||||
| chr16:89865965
|
C | CA | 79 | a0001c0001t0001g0054a0001c0001t0001g0081a0001c0001t0001g0083others(76): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1778+2126dupA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89865965 | |||||
| chr16:89865965
|
C | CAA | 44 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0068others(41): Show | 44 | HG00642.hp1 HG00733.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.1778+2125_1778+212 others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89865965 | |||||
| chr16:89865965
|
C | CAAA | 7 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0118others(4): Show | 7 | HG01123.hp1 HG01934.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1778+2124_1778+212 others(7): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89865965 | |||||
| chr16:89865965
|
CA | C | 55 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0223others(52): Show | 55 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1778+2126delA | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89865965 | |||||
| chr16:89866112
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1779-2077G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866112 | ||||||
| chr16:89866139
|
A | AC | 355 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(352): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1779-2048dupC | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89866139 | |||||
| chr16:89866168
|
T | C | 7 | a0001c0003t0001g0274a0001c0003t0001g0277a0001c0003t0005g0273others(4): Show | 7 | HG00280.hp1 NA18970.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1779-2021T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866168 | ||||||
| chr16:89866308
|
T | C | 11 | a0001c0001t0001g0071a0001c0001t0001g0161a0001c0006t0001g0007others(8): Show | 11 | HG00099.hp2 HG01192.hp1 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.1779-1881T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866308 | ||||||
| chr16:89866492
|
C | G | 1 | a0001c0001t0015g0229 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1779-1697C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866492 | ||||||
| chr16:89866523
|
C | G | 33 | a0001c0001t0002g0051a0001c0001t0002g0122a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1779-1666C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866523 | ||||||
| chr16:89866586
|
C | T | 22 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0003g0320others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1779-1603C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866586 | ||||||
| chr16:89866599
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(183): Show | 186 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1779-1590A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866599 | ||||||
| chr16:89866599
|
A | T | 2 | a0002c0002t0002g0027a0002c0002t0002g0043 | 2 | HG02056.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1779-1590A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866599 | ||||||
| chr16:89866599
|
AT | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0054others(119): Show | 122 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1779-1577delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89866599 | |||||
| chr16:89866672
|
A | G | 1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1779-1517A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866672 | ||||||
| chr16:89866898
|
C | T | 33 | a0001c0001t0002g0051a0001c0001t0002g0122a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1779-1291C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866898 | ||||||
| chr16:89866916
|
T | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(131): Show | 134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1779-1273T>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89866916 | ||||||
| chr16:89867012
|
A | G | 55 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0002g0051others(52): Show | 55 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1779-1177A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867012 | ||||||
| chr16:89867093
|
CTT | C | 8 | a0001c0006t0001g0007a0001c0006t0001g0012a0001c0006t0001g0013others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.1779-1094_1779-109 others(6): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89867093 | |||||
| chr16:89867101
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1779-1088G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867101 | ||||||
| chr16:89867124
|
G | T | 1 | a0003c0005t0001g0295 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1779-1065G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867124 | ||||||
| chr16:89867160
|
T | C | 3 | a0001c0019t0001g0317a0006c0010t0001g0314a0006c0010t0008g0313 | 3 | HG02451.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1779-1029T>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867160 | ||||||
| chr16:89867194
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG02559.hp2 HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1779-995C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867194 | ||||||
| chr16:89867213
|
C | T | 6 | a0001c0001t0001g0087a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG00733.hp2 HG01071.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1779-976C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867213 | ||||||
| chr16:89867264
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1779-925C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867264 | ||||||
| chr16:89867304
|
C | T | 1 | a0001c0001t0001g0002 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1779-885C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867304 | ||||||
| chr16:89867306
|
GC | G | 35 | a0001c0001t0001g0057a0001c0001t0001g0083a0001c0001t0001g0105others(32): Show | 35 | HG00280.hp1 HG00597.hp1 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.1779-882delC | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867306 | ||||||
| chr16:89867369
|
A | G | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG02738.hp1 HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1779-820A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867369 | ||||||
| chr16:89867421
|
G | T | 2 | a0001c0019t0001g0317a0006c0010t0001g0314 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1779-768G>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867421 | ||||||
| chr16:89867443
|
G | A | 34 | a0001c0001t0001g0057a0001c0001t0001g0105a0001c0001t0001g0106others(31): Show | 34 | HG00280.hp1 HG00597.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.1779-746G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867443 | ||||||
| chr16:89867451
|
G | A | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1779-738G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867451 | ||||||
| chr16:89867587
|
A | AT | 119 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0057others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1779-587dupT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 89867587 | |||||
| chr16:89867646
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1779-543G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867646 | ||||||
| chr16:89867841
|
T | A | 1 | a0001c0003t0001g0101 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1779-348T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89867841 | ||||||
| chr16:89868115
|
C | T | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1779-74C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89868115 | ||||||
| chr16:89868122
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1779-67C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 12/14 | chr16 | 89868122 | ||||||
| chr16:89868346
|
C | T | 1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1806+130C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868346 | ||||||
| chr16:89868391
|
G | C | 2 | a0004c0004t0001g0187a0004c0004t0001g0205 | 2 | NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1806+175G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868391 | ||||||
| chr16:89868425
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1806+209C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868425 | ||||||
| chr16:89868437
|
C | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0087 | 3 | HG00733.hp2 HG01106.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1806+221C>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868437 | ||||||
| chr16:89868478
|
A | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0091others(123): Show | 126 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1806+262A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868478 | ||||||
| chr16:89868681
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1806+465C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868681 | ||||||
| chr16:89868891
|
C | T | 2 | a0001c0001t0001g0160a0001c0019t0001g0317 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1806+675C>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89868891 | ||||||
| chr16:89869032
|
A | T | 1 | a0001c0001t0001g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1807-535A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869032 | ||||||
| chr16:89869045
|
A | AACATATA others(19): Show |
1 | a0002c0002t0002g0038 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1807-521_1807-520i others(28): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869045 | |||||
| chr16:89869045
|
A | ACAT | 3 | a0002c0002t0014g0044a0005c0007t0002g0032a0005c0014t0002g0021 | 3 | HG00621.hp1 HG02040.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1807-522_1807-521i others(5): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | ||||||
| chr16:89869045
|
A | ACATATAT others(6): Show |
1 | a0002c0002t0002g0047 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1807-522_1807-521i others(15): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | ||||||
| chr16:89869045
|
A | ACATATAT others(10): Show |
1 | a0016c0015t0002g0049 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1807-522_1807-521i others(19): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | ||||||
| chr16:89869045
|
A | ACATATAT others(12): Show |
8 | a0001c0001t0002g0051a0002c0002t0002g0028a0002c0002t0002g0031others(5): Show | 8 | HG00673.hp1 HG02015.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1807-522_1807-521i others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | ||||||
| chr16:89869045
|
A | ACATATAT others(14): Show |
2 | a0002c0002t0002g0029a0002c0002t0002g0043 | 2 | HG02056.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1807-522_1807-521i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | ||||||
| chr16:89869045
|
A | ACATATAT others(16): Show |
4 | a0002c0002t0002g0027a0002c0002t0002g0035a0002c0002t0002g0053others(1): Show | 4 | HG02165.hp1 NA18943.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807-522_1807-521i others(25): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | ||||||
| chr16:89869045
|
A | ACATATAT others(18): Show |
2 | a0002c0002t0002g0034a0002c0002t0002g0048 | 2 | HG02074.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1807-522_1807-521i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | ||||||
| chr16:89869045
|
A | ACATATAT others(20): Show |
1 | a0002c0002t0002g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1807-522_1807-521i others(29): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | ||||||
| chr16:89869045
|
A | ACATATAT others(24): Show |
2 | a0002c0002t0002g0023a0002c0002t0002g0045 | 2 | HG00323.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1807-522_1807-521i others(33): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | ||||||
| chr16:89869045
|
A | ACATATAT others(26): Show |
3 | a0001c0001t0002g0122a0002c0002t0002g0030a0005c0007t0002g0052 | 3 | HG00609.hp1 HG00621.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1807-522_1807-521i others(35): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | ||||||
| chr16:89869045
|
A | ACATATAT others(30): Show |
2 | a0002c0002t0002g0024a0005c0007t0002g0036 | 2 | HG01175.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1807-522_1807-521i others(39): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869045 | ||||||
| chr16:89869047
|
A | AACATATA others(25): Show |
1 | a0001c0001t0003g0320 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1807-519_1807-518i others(34): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869047 | |||||
| chr16:89869047
|
A | T | 33 | a0001c0001t0002g0051a0001c0001t0002g0122a0002c0002t0002g0022others(30): Show | 33 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1807-520A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869047 | ||||||
| chr16:89869049
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0083 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1807-518_1807-517i others(15): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869049 | ||||||
| chr16:89869049
|
A | ATATATAT others(20): Show |
1 | a0001c0006t0001g0012 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1807-518_1807-517i others(29): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869049 | ||||||
| chr16:89869049
|
A | T | 34 | a0001c0001t0002g0051a0001c0001t0002g0122a0001c0001t0003g0320others(31): Show | 34 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1807-518A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869049 | ||||||
| chr16:89869051
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0130a0006c0010t0001g0314 | 2 | HG02683.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1807-516_1807-515i others(15): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869051 | ||||||
| chr16:89869051
|
A | ATATATAT others(18): Show |
1 | a0012c0017t0001g0148 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1807-516_1807-515i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869051 | ||||||
| chr16:89869051
|
A | T | 36 | a0001c0001t0001g0083a0001c0001t0002g0051a0001c0001t0002g0122others(33): Show | 36 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.1807-516A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869051 | ||||||
| chr16:89869053
|
A | AAAAAAAA others(46): Show |
1 | a0001c0009t0001g0017 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(55): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0001g0240 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(39): Show |
1 | a0001c0001t0010g0348 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(48): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(49): Show |
1 | a0001c0001t0001g0232 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(58): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0283 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0001g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(35): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(32): Show |
1 | a0001c0001t0001g0188 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(34): Show |
2 | a0001c0001t0009g0174a0004c0004t0001g0173 | 2 | HG00408.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0099 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(30): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(29): Show |
1 | a0004c0004t0001g0205 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(38): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(18): Show |
1 | a0004c0004t0001g0186 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(26): Show |
2 | a0001c0001t0001g0222a0001c0001t0001g0235 | 2 | HG01261.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(35): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0001g0202 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(32): Show |
2 | a0001c0001t0001g0216a0001c0001t0001g0246 | 2 | HG02300.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(40): Show |
2 | a0001c0001t0001g0219a0001c0001t0001g0347 | 2 | HG00733.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(49): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(11): Show |
1 | a0001c0018t0012g0346 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0149 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(26): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0059 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(32): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0239 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(34): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0011g0217 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(36): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(33): Show |
3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213 | 3 | NA19000.hp2 NA19007.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(37): Show |
1 | a0001c0001t0001g0225 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(10): Show |
1 | a0015c0023t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(19): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(12): Show |
3 | a0001c0001t0001g0107a0001c0001t0001g0162a0001c0001t0001g0184 | 3 | HG00597.hp1 NA18522.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(14): Show |
4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG02615.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(24): Show |
1 | a0007c0026t0001g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(33): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(28): Show |
2 | a0001c0001t0001g0209a0001c0001t0001g0238 | 2 | NA18612.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(34): Show |
1 | a0001c0001t0001g0261 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(36): Show |
1 | a0001c0001t0001g0236 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(45): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(38): Show |
1 | a0001c0001t0001g0253 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(47): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0085 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(18): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(11): Show |
7 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0105others(4): Show | 7 | HG01928.hp2 HG01952.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(13): Show |
5 | a0001c0001t0001g0245a0001c0001t0001g0352a0001c0003t0001g0120others(2): Show | 5 | HG02293.hp2 HG03942.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(22): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(17): Show |
1 | a0004c0004t0001g0187 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(26): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(28): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(23): Show |
2 | a0001c0001t0001g0002a0001c0001t0001g0185 | 2 | NA19000.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(32): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(25): Show |
4 | a0001c0001t0001g0171a0001c0001t0001g0210a0001c0001t0001g0214others(1): Show | 4 | NA18979.hp2 NA18982.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(34): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(27): Show |
5 | a0001c0001t0001g0190a0001c0001t0001g0254a0001c0001t0001g0257others(2): Show | 5 | HG02027.hp1 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(36): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(29): Show |
2 | a0001c0001t0001g0176a0004c0004t0001g0196 | 2 | HG01358.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(38): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0001g0091 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(33): Show |
1 | a0001c0001t0004g0316 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(35): Show |
1 | a0001c0001t0001g0233 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(44): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(37): Show |
1 | a0001c0001t0001g0237 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(41): Show |
1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(50): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(4): Show |
3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG00642.hp1 HG01074.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(13): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(17): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(10): Show |
10 | a0001c0001t0001g0108a0001c0001t0001g0158a0001c0001t0001g0287others(7): Show | 10 | HG00741.hp1 HG01106.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(19): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(12): Show |
7 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0282others(4): Show | 7 | HG00323.hp2 HG01891.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(14): Show |
2 | a0001c0003t0005g0275a0001c0003t0005g0276 | 2 | NA18983.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0123 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(29): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0266 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(31): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(26): Show |
3 | a0001c0001t0001g0100a0001c0001t0001g0192a0004c0004t0001g0197 | 3 | HG02015.hp2 NA18940.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(35): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(28): Show |
3 | a0001c0001t0001g0183a0001c0001t0001g0218a0001c0001t0004g0259 | 3 | HG00673.hp2 NA18971.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(30): Show |
4 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(39): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(32): Show |
3 | a0001c0001t0001g0071a0001c0001t0001g0226a0001c0001t0004g0244 | 3 | HG00099.hp2 HG02165.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(34): Show |
2 | a0001c0001t0001g0075a0001c0001t0001g0169 | 2 | HG01168.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(38): Show |
1 | a0001c0001t0001g0242 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(47): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(40): Show |
1 | a0013c0020t0001g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(49): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0072 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(12): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(11): Show |
7 | a0001c0001t0001g0084a0001c0001t0001g0118a0001c0001t0001g0291others(4): Show | 7 | HG01106.hp1 HG02148.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(13): Show |
9 | a0001c0001t0001g0104a0001c0001t0001g0134a0001c0001t0001g0163others(6): Show | 9 | HG02071.hp1 HG02622.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(22): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(17): Show |
3 | a0001c0001t0001g0131a0001c0001t0001g0292a0001c0001t0001g0294 | 3 | HG00099.hp1 HG01978.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(26): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(30): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(25): Show |
2 | a0001c0001t0001g0264a0001c0001t0001g0269 | 2 | HG01256.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(34): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(27): Show |
2 | a0001c0001t0001g0006a0001c0001t0001g0221 | 2 | HG01255.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(36): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(29): Show |
3 | a0001c0001t0001g0076a0001c0001t0001g0247a0004c0004t0001g0195 | 3 | HG01074.hp2 HG03927.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(38): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(31): Show |
5 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0207others(2): Show | 5 | NA18945.hp1 NA18945.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(33): Show |
4 | a0001c0001t0001g0198a0001c0001t0001g0223a0001c0001t0001g0265others(1): Show | 4 | NA18943.hp2 NA19060.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAA others(35): Show |
1 | a0001c0009t0001g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(44): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAC others(24): Show |
1 | a0001c0001t0003g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(33): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAC others(28): Show |
1 | a0001c0001t0003g0329 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAC others(34): Show |
1 | a0001c0001t0003g0344 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAC others(38): Show |
1 | a0001c0001t0003g0343 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(47): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAT others(4): Show |
1 | a0004c0004t0001g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(13): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAT others(10): Show |
1 | a0001c0001t0001g0126 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(19): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAT others(12): Show |
6 | a0001c0001t0001g0152a0001c0001t0001g0263a0001c0001t0001g0289others(3): Show | 6 | HG00280.hp1 HG01123.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAT others(14): Show |
3 | a0001c0001t0001g0151a0001c0001t0001g0249a0001c0003t0001g0277 | 3 | HG02258.hp2 HG02970.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAT others(16): Show |
1 | a0001c0001t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(25): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAT others(24): Show |
2 | a0001c0001t0001g0189a0001c0001t0001g0267 | 2 | NA18951.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(33): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAT others(28): Show |
2 | a0001c0001t0004g0262a0001c0001t0015g0229 | 2 | HG01256.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAT others(34): Show |
1 | a0011c0022t0001g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAAAT others(38): Show |
1 | a0001c0001t0001g0069 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(47): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAACA others(7): Show |
1 | a0001c0001t0003g0340 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(16): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAACA others(25): Show |
1 | a0001c0001t0003g0330 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(34): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAACA others(27): Show |
1 | a0001c0001t0003g0331 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(36): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAACA others(31): Show |
1 | a0001c0001t0003g0341 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAACA others(37): Show |
2 | a0001c0001t0003g0323a0001c0001t0003g0342 | 2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(5): Show |
1 | a0006c0010t0008g0313 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(11): Show |
10 | a0001c0001t0001g0068a0001c0001t0001g0087a0001c0001t0001g0106others(7): Show | 10 | HG00733.hp2 HG01071.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(13): Show |
7 | a0001c0001t0001g0110a0001c0001t0001g0156a0001c0001t0001g0172others(4): Show | 7 | HG00408.hp2 HG01884.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(22): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(15): Show |
2 | a0001c0001t0001g0114a0001c0001t0001g0160 | 2 | HG02027.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(24): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(21): Show |
1 | a0001c0001t0001g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(30): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(25): Show |
3 | a0001c0001t0001g0256a0001c0001t0001g0268a0014c0024t0001g0270 | 3 | HG02071.hp2 HG03927.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(34): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(27): Show |
4 | a0001c0001t0001g0227a0001c0001t0001g0303a0001c0001t0004g0224others(1): Show | 4 | HG00280.hp2 HG01168.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1807-513_1807-512i others(36): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(29): Show |
1 | a0001c0001t0004g0230 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(38): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(31): Show |
1 | a0001c0001t0001g0234 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(40): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(33): Show |
1 | a0001c0001t0001g0182 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(42): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(35): Show |
2 | a0001c0001t0001g0168a0001c0001t0001g0206 | 2 | HG00438.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(44): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(39): Show |
1 | a0001c0001t0001g0243 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(48): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAAATA others(51): Show |
1 | a0001c0001t0001g0241 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(60): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAACAT others(30): Show |
1 | a0001c0001t0003g0338 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(39): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAATAT others(10): Show |
2 | a0003c0005t0001g0311a0003c0005t0001g0312 | 2 | HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(19): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAATAT others(12): Show |
2 | a0001c0001t0001g0308a0001c0001t0001g0322 | 2 | HG01109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(21): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAATAT others(14): Show |
1 | a0001c0001t0001g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAATAT others(16): Show |
3 | a0001c0001t0001g0147a0001c0001t0001g0290a0001c0001t0001g0293 | 3 | HG00735.hp2 HG01358.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(25): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAATAT others(22): Show |
3 | a0001c0001t0001g0138a0001c0001t0001g0143a0001c0001t0001g0251 | 3 | HG02976.hp2 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(31): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAATAT others(26): Show |
3 | a0001c0001t0001g0215a0001c0001t0004g0170a0001c0027t0001g0020 | 3 | HG01169.hp2 HG03831.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(35): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAATAT others(28): Show |
1 | a0001c0001t0001g0302 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAAATAT others(32): Show |
1 | a0001c0003t0001g0165 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAACAAA others(37): Show |
1 | a0001c0001t0001g0337 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0177 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAATATA others(7): Show |
1 | a0001c0001t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(16): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAATATA others(9): Show |
1 | a0003c0005t0001g0309 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(18): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAATATA others(11): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0157 | 2 | HG01516.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAATATA others(15): Show |
2 | a0001c0001t0001g0150a0001c0019t0001g0317 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(24): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAATATA others(17): Show |
1 | a0001c0001t0001g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(26): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAATATA others(21): Show |
1 | a0001c0001t0001g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(30): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAAATATA others(23): Show |
2 | a0001c0001t0001g0137a0001c0001t0001g0144 | 2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(32): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAACAAAC others(37): Show |
1 | a0001c0001t0003g0326 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(46): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAACAAAC others(30): Show |
1 | a0001c0001t0003g0345 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(39): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAACAAAC others(32): Show |
1 | a0001c0001t0003g0336 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAACAAAC others(34): Show |
1 | a0001c0001t0003g0335 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAACAAAC others(36): Show |
2 | a0001c0001t0001g0328a0001c0001t0003g0325 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(45): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAACAAAC others(38): Show |
1 | a0001c0001t0003g0332 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(47): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAACAAAC others(32): Show |
2 | a0001c0001t0003g0333a0001c0001t0003g0334 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1807-513_1807-512i others(41): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAATATAT others(6): Show |
1 | a0001c0001t0001g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(15): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAATATAT others(14): Show |
1 | a0001c0012t0005g0272 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAATATAT others(18): Show |
1 | a0001c0001t0001g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAATATAT others(20): Show |
1 | a0001c0001t0001g0125 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(29): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAATATAT others(22): Show |
1 | a0001c0001t0001g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(31): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAATATAT others(28): Show |
1 | a0001c0001t0001g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1807-513_1807-512i others(37): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AAATATAT others(34): Show |
1 | a0001c0001t0004g0315 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1807-513_1807-512i others(43): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AATATATA others(13): Show |
1 | a0001c0001t0001g0199 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1807-511_1807-492d others(22): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0193 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1807-513_1807-492d others(24): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869053 | |||||
| chr16:89869053
|
A | ATATATAT others(4): Show |
1 | a0003c0005t0001g0310 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1807-514_1807-513i others(13): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869053 | ||||||
| chr16:89869053
|
A | ATATATAT others(14): Show |
1 | a0001c0006t0001g0013 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1807-514_1807-513i others(23): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869053 | ||||||
| chr16:89869053
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0203 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1807-514_1807-513i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869053 | ||||||
| chr16:89869053
|
A | ATATATAT others(24): Show |
1 | a0001c0006t0001g0014 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1807-514_1807-513i others(33): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869053 | ||||||
| chr16:89869053
|
A | T | 45 | a0001c0001t0001g0067a0001c0001t0001g0074a0001c0001t0001g0083others(42): Show | 45 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1807-514A>T | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869053 | ||||||
| chr16:89869054
|
AT | A | 3 | a0001c0001t0001g0284a0001c0008t0001g0010a0001c0011t0001g0318 | 3 | HG02572.hp2 HG02647.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1807-512delT | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869054 | ||||||
| chr16:89869055
|
T | A | 8 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(5): Show | 8 | HG01081.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1807-512T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869055 | ||||||
| chr16:89869057
|
T | A | 7 | a0001c0001t0001g0004a0001c0008t0001g0009a0001c0008t0001g0010others(4): Show | 7 | HG01081.hp1 HG01167.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1807-510T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869057 | ||||||
| chr16:89869059
|
T | A | 5 | a0001c0001t0001g0004a0001c0008t0001g0008a0001c0008t0001g0010others(2): Show | 5 | HG01167.hp2 HG02572.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1807-508T>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869059 | ||||||
| chr16:89869072
|
A | ATATATAT others(23): Show |
1 | a0001c0006t0001g0007 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1807-492_1807-491i others(32): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | |||||
| chr16:89869072
|
A | ATATATAT others(21): Show |
1 | a0001c0006t0001g0016 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1807-492_1807-491i others(30): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | |||||
| chr16:89869072
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0141 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1807-492_1807-491i others(22): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | |||||
| chr16:89869072
|
A | ATATATAT others(11): Show |
1 | a0001c0003t0001g0278 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1807-492_1807-491i others(20): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | |||||
| chr16:89869072
|
A | ATATATAT others(18): Show |
1 | a0001c0009t0001g0019 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1807-492_1807-491i others(27): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | |||||
| chr16:89869072
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0111 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1807-492_1807-491i others(14): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | |||||
| chr16:89869072
|
A | ATGTATG | 5 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG00642.hp1 HG01074.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1807-494_1807-493i others(8): Show |
SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 89869072 | |||||
| chr16:89869072
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0057others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1807-495A>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869072 | ||||||
| chr16:89869239
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1807-328G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869239 | ||||||
| chr16:89869302
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1807-265G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 13/14 | chr16 | 89869302 | ||||||
| chr16:89869725
|
G | C | 1 | a0001c0001t0001g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1922+43G>C | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 14/14 | chr16 | 89869725 | ||||||
| chr16:89869745
|
G | A | 1 | a0003c0005t0001g0312 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1922+63G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 14/14 | chr16 | 89869745 | ||||||
| chr16:89869746
|
C | G | 1 | a0001c0001t0003g0329 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1922+64C>G | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 14/14 | chr16 | 89869746 | ||||||
| chr16:89869817
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1922+135G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 14/14 | chr16 | 89869817 | ||||||
| chr16:89869959
|
G | A | 1 | a0001c0001t0003g0344 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1923-91G>A | SPIRE2 | ENSG00000204991.11 | transcript | ENST00000378247.8 | protein_coding | 14/14 | chr16 | 89869959 |