Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 441631 |
|---|---|
| ensemblid | ENSG00000110900.16 |
| hgncid | 30795 |
| symbol | TSPAN11 |
| name | tetraspanin 11 |
| refseq_nuc | NM_001370302.1 |
| refseq_prot | NP_001357231.1 |
| ensembl_nuc | ENST00000546076.6 |
| ensembl_prot | ENSP00000437403.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 30926748 |
| end | 30996599 |
| strand | + |
| ver | v1.2 |
| region | chr12:30926748-30996599 |
| region5000 | chr12:30921748-31001599 |
| regionname0 | TSPAN11_chr12_30926748_30996599 |
| regionname5000 | TSPAN11_chr12_30921748_31001599 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 253 | 245 | 59 | 55 | 89 | 9 | 32 | 66 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002 | 1/0 | 253 | 120 | 33 | 17 | 57 | 2 | 10 | 40 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003 | 0/0 | 253 | 17 | 0 | 1 | 11 | 1 | 4 | 8 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0004 | 0/0 | 253 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0005 | 0/0 | 253 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0006 | 0/0 | 253 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0007 | 0/0 | 253 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0008 | 0/0 | 253 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0009 | 0/0 | 253 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0010 | 0/0 | 253 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0011 | 0/0 | 253 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0012 | 0/0 | 253 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 762 | 241 | 57 | 55 | 87 | 9 | 32 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0002 | 0/0 | 762 | 102 | 29 | 12 | 52 | 1 | 8 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0003 | 0/0 | 762 | 17 | 0 | 1 | 11 | 1 | 4 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0004 | 1/0 | 762 | 15 | 1 | 5 | 5 | 1 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0005 | 0/0 | 762 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0006 | 0/0 | 762 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0007 | 0/0 | 762 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0008 | 0/0 | 762 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0009 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0010 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0011 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0012 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0013 | 0/0 | 762 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0014 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0015 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0016 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| c0017 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4744 | 71 | 6 | 3 | 54 | 1 | 7 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0002 | 0/1 | 4748 | 46 | 7 | 21 | 4 | 3 | 10 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0003 | 0/0 | 4744 | 29 | 0 | 0 | 27 | 0 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0004 | 0/0 | 4748 | 23 | 13 | 9 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0005 | 0/0 | 4744 | 21 | 0 | 5 | 8 | 1 | 7 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0006 | 0/0 | 4744 | 19 | 2 | 0 | 16 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0007 | 0/0 | 4744 | 18 | 0 | 0 | 17 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0008 | 0/0 | 4744 | 14 | 0 | 0 | 14 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0009 | 0/0 | 4748 | 11 | 2 | 8 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0010 | 0/0 | 4745 | 10 | 3 | 5 | 0 | 1 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0011 | 0/0 | 4744 | 9 | 0 | 6 | 3 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0012 | 0/0 | 4744 | 8 | 0 | 0 | 8 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0013 | 0/0 | 4744 | 7 | 7 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0014 | 0/0 | 4745 | 5 | 3 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0015 | 0/0 | 4748 | 5 | 4 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0016 | 0/0 | 4746 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0017 | 0/0 | 4741 | 5 | 0 | 3 | 0 | 0 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0018 | 0/0 | 4747 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0019 | 0/0 | 4744 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0020 | 0/0 | 4744 | 3 | 1 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0021 | 0/0 | 4744 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0022 | 0/0 | 4744 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0023 | 0/0 | 4745 | 3 | 0 | 1 | 0 | 2 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0024 | 0/0 | 4744 | 3 | 2 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0025 | 0/0 | 4744 | 3 | 0 | 1 | 0 | 0 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0026 | 0/0 | 4744 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0027 | 0/0 | 4744 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0028 | 0/0 | 4749 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0029 | 0/0 | 4745 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0030 | 0/0 | 4748 | 2 | 0 | 1 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0031 | 0/0 | 4749 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0032 | 0/0 | 4744 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0033 | 0/0 | 4744 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0034 | 0/0 | 4744 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0035 | 0/0 | 4748 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0036 | 0/0 | 4744 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0037 | 0/0 | 4744 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0038 | 0/0 | 4744 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0039 | 0/0 | 4748 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0040 | 0/0 | 4748 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0041 | 0/0 | 4744 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0042 | 0/0 | 4748 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0043 | 0/0 | 4748 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0044 | 0/0 | 4744 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0045 | 0/0 | 4744 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0046 | 0/0 | 4744 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0047 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0048 | 0/0 | 4744 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0049 | 0/0 | 4748 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0050 | 0/0 | 4748 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0051 | 0/0 | 4744 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0052 | 0/0 | 4745 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0053 | 0/0 | 4741 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0054 | 1/0 | 4745 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0055 | 0/0 | 4748 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0056 | 0/0 | 4744 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0057 | 0/0 | 4748 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0058 | 0/0 | 4748 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0059 | 0/0 | 4748 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0060 | 0/0 | 4744 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0061 | 0/0 | 4744 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0062 | 0/0 | 4744 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0063 | 0/0 | 4748 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0064 | 0/0 | 4749 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0065 | 0/0 | 4744 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0066 | 0/0 | 4744 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0067 | 0/0 | 4744 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0068 | 0/0 | 4748 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0069 | 0/0 | 4744 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0070 | 0/0 | 4744 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0071 | 0/0 | 4744 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0072 | 0/0 | 4748 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0073 | 0/0 | 4744 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0074 | 0/0 | 4744 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0075 | 0/0 | 4744 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| t0076 | 0/0 | 4747 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0311 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 762 | 241 | 57 | 55 | 87 | 9 | 32 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0007 | 0/0 | 762 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0008 | 0/0 | 762 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002 | 0/0 | 762 | 102 | 29 | 12 | 52 | 1 | 8 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0004 | 1/0 | 762 | 15 | 1 | 5 | 5 | 1 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0005 | 0/0 | 762 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003 | 0/0 | 762 | 17 | 0 | 1 | 11 | 1 | 4 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0004c0006 | 0/0 | 762 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0004c0016 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0005c0017 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0006c0013 | 0/0 | 762 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0007c0009 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0008c0011 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0009c0015 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0010c0012 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0011c0010 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0012c0014 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5505 | 34 | 6 | 2 | 21 | 1 | 4 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0002 | 0/1 | 5509 | 40 | 3 | 20 | 3 | 3 | 10 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0003 | 0/0 | 5505 | 25 | 0 | 0 | 23 | 0 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0004 | 0/0 | 5509 | 8 | 6 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0005 | 0/0 | 5505 | 12 | 0 | 5 | 3 | 1 | 3 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0006 | 0/0 | 5505 | 12 | 2 | 0 | 9 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0007 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0008 | 0/0 | 5505 | 12 | 0 | 0 | 12 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0009 | 0/0 | 5509 | 10 | 2 | 7 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0010 | 0/0 | 5506 | 9 | 3 | 5 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0011 | 0/0 | 5505 | 7 | 0 | 5 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0012 | 0/0 | 5505 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0014 | 0/0 | 5506 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0015 | 0/0 | 5509 | 4 | 3 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0016 | 0/0 | 5507 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0017 | 0/0 | 5502 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0018 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0019 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0020 | 0/0 | 5505 | 3 | 1 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0021 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0022 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0023 | 0/0 | 5506 | 3 | 0 | 1 | 0 | 2 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0024 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0025 | 0/0 | 5505 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0027 | 0/0 | 5505 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0028 | 0/0 | 5510 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0029 | 0/0 | 5506 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0031 | 0/0 | 5510 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0032 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0033 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0034 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0036 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0037 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0039 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0040 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0042 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0043 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0044 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0048 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0049 | 0/0 | 5509 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0051 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0055 | 0/0 | 5509 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0056 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0057 | 0/0 | 5509 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0058 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0059 | 0/0 | 5509 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0063 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0064 | 0/0 | 5510 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0065 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0067 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0069 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0070 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0071 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0001t0076 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0007t0013 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0001c0008t0001 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0001 | 0/0 | 5505 | 27 | 0 | 1 | 24 | 0 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0002 | 0/0 | 5509 | 5 | 4 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0003 | 0/0 | 5505 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0004 | 0/0 | 5509 | 11 | 4 | 6 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0005 | 0/0 | 5505 | 5 | 0 | 0 | 3 | 0 | 2 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0006 | 0/0 | 5505 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0007 | 0/0 | 5505 | 14 | 0 | 0 | 13 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0012 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0013 | 0/0 | 5505 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0014 | 0/0 | 5506 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0015 | 0/0 | 5509 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0018 | 0/0 | 5508 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0021 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0024 | 0/0 | 5505 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0025 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0026 | 0/0 | 5505 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0030 | 0/0 | 5509 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0038 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0041 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0045 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0046 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0047 | 0/0 | 5507 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0060 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0061 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0066 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0072 | 0/0 | 5509 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0073 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0074 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0002t0075 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0004t0001 | 0/0 | 5505 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0004t0004 | 0/0 | 5509 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0004t0005 | 0/0 | 5505 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0004t0014 | 0/0 | 5506 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0004t0017 | 0/0 | 5502 | 4 | 0 | 3 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0004t0030 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0004t0053 | 0/0 | 5502 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0004t0054 | 1/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0002c0005t0004 | 0/0 | 5509 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0001 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0003 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0005 | 0/0 | 5505 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0006 | 0/0 | 5505 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0008 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0009 | 0/0 | 5509 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0010 | 0/0 | 5506 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0012 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0032 | 0/0 | 5505 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0035 | 0/0 | 5509 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0052 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0062 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0003c0003t0068 | 0/0 | 5509 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0004c0006t0001 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0004c0006t0007 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0004c0016t0007 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0005c0017t0011 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0006c0013t0011 | 0/0 | 5505 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0007c0009t0001 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0008c0011t0002 | 0/0 | 5509 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0009c0015t0019 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0010c0012t0050 | 0/0 | 5509 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0011c0010t0022 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| a0012c0014t0019 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | copy fasta | chr12 | 30921748 | 31001599 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0002g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0003g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0004g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0005g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0005g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0005g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0005g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0005g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0008g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0008g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0008g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0009g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0009g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0009g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0009g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0009g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0009g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0009g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0009g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0009g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0010g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0010g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0010g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0010g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0010g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0010g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0010g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0011g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0011g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0011g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0011g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0011g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0011g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0012g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0012g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0012g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0012g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0012g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0014g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0014g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0015g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0015g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0015g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0015g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0016g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0016g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0016g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0016g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0016g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0017g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0018g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0019g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0019g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0020g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0020g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0020g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0021g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0021g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0022g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0022g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0023g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0023g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0023g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0024g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0024g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0025g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0025g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0027g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0027g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0028g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0028g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0029g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0029g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0031g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0031g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0032g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0033g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0033g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0034g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0034g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0036g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0037g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0039g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0040g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0042g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0043g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0044g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0048g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0049g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0051g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0055g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0056g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0057g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0058g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0059g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0063g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0064g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0065g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0067g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0069g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0070g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0071g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0001t0076g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0007t0013g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0007t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0008t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0001c0008t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0004g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0004g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0005g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0005g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0007g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0012g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0012g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0013g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0013g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0013g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0013g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0014g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0014g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0015g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0018g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0018g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0018g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0018g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0021g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0024g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0025g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0026g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0026g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0026g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0030g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0038g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0041g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0045g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0046g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0047g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0060g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0061g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0066g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0072g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0073g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0074g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0002t0075g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0005g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0014g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0017g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0017g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0017g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0030g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0053g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0004t0054g0311 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0005t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0005t0004g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0002c0005t0004g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0008g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0008g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0009g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0010g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0012g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0032g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0035g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0052g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0062g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0003c0003t0068g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0004c0006t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0004c0006t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0004c0006t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0004c0016t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0005c0017t0011g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0006c0013t0011g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0007c0009t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0008c0011t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0009c0015t0019g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0010c0012t0050g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0011c0010t0022g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| a0012c0014t0019g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0003 | c0003 | t0010 | g0161 | EUR | GBR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0290 | EUR | GBR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00280 | hp1 | a0001 | c0001 | t0043 | g0256 | EUR | FIN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0220 | EUR | FIN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00323 | hp2 | a0002 | c0002 | t0007 | g0076 | EUR | FIN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00408 | hp2 | a0001 | c0001 | t0032 | g0268 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00423 | hp1 | a0008 | c0011 | t0002 | g0260 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0375 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00438 | hp2 | a0002 | c0002 | t0007 | g0150 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00544 | hp2 | a0001 | c0001 | t0067 | g0305 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0159 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0030 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00639 | hp2 | a0003 | c0003 | t0009 | g0162 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00642 | hp1 | a0001 | c0001 | t0009 | g0329 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00642 | hp2 | a0001 | c0001 | t0010 | g0273 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00673 | hp1 | a0003 | c0003 | t0012 | g0216 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00673 | hp2 | a0002 | c0002 | t0007 | g0251 | EAS | CHS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00733 | hp1 | a0001 | c0001 | t0009 | g0348 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0277 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0325 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0341 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00738 | hp1 | a0002 | c0004 | t0014 | g0195 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00738 | hp2 | a0002 | c0002 | t0004 | g0300 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00741 | hp1 | a0001 | c0001 | t0010 | g0050 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG00741 | hp2 | a0002 | c0002 | t0004 | g0323 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01069 | hp2 | a0002 | c0004 | t0004 | g0283 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01070 | hp1 | a0002 | c0002 | t0030 | g0308 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01070 | hp2 | a0002 | c0004 | t0017 | g0003 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01071 | hp1 | a0002 | c0004 | t0017 | g0003 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01074 | hp1 | a0002 | c0002 | t0004 | g0373 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0303 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0157 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01106 | hp1 | a0001 | c0001 | t0009 | g0204 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01109 | hp1 | a0002 | c0002 | t0024 | g0155 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0346 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01167 | hp1 | a0002 | c0002 | t0014 | g0124 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01167 | hp2 | a0001 | c0001 | t0020 | g0017 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01168 | hp1 | a0001 | c0001 | t0010 | g0335 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01169 | hp2 | a0001 | c0001 | t0020 | g0018 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01192 | hp1 | a0001 | c0001 | t0015 | g0366 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0231 | AMR | PUR | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01255 | hp1 | a0002 | c0002 | t0004 | g0096 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01255 | hp2 | a0002 | c0002 | t0072 | g0153 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01257 | hp1 | a0001 | c0001 | t0009 | g0372 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0377 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0345 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0378 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01358 | hp1 | a0001 | c0001 | t0055 | g0172 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01358 | hp2 | a0001 | c0001 | t0009 | g0271 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01361 | hp2 | a0002 | c0002 | t0004 | g0379 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0079 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01433 | hp2 | a0001 | c0001 | t0023 | g0170 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0376 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0344 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01516 | hp1 | a0001 | c0001 | t0023 | g0337 | EUR | IBS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01516 | hp2 | a0002 | c0004 | t0030 | g0206 | EUR | IBS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01517 | hp1 | a0001 | c0001 | t0023 | g0336 | EUR | IBS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0163 | EUR | IBS | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01884 | hp1 | a0001 | c0001 | t0034 | g0008 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01884 | hp2 | a0002 | c0002 | t0041 | g0012 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01891 | hp1 | a0011 | c0010 | t0022 | g0185 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01891 | hp2 | a0002 | c0002 | t0018 | g0201 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01928 | hp2 | a0001 | c0001 | t0031 | g0207 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0380 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01934 | hp2 | a0002 | c0002 | t0004 | g0021 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01943 | hp2 | a0001 | c0001 | t0010 | g0209 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01952 | hp2 | a0001 | c0001 | t0011 | g0340 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01975 | hp1 | a0001 | c0001 | t0011 | g0339 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01978 | hp1 | a0001 | c0001 | t0064 | g0208 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01978 | hp2 | a0006 | c0013 | t0011 | g0338 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01981 | hp1 | a0002 | c0004 | t0017 | g0152 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0048 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02004 | hp1 | a0001 | c0001 | t0031 | g0102 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02004 | hp2 | a0001 | c0001 | t0011 | g0221 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02015 | hp2 | a0001 | c0001 | t0006 | g0285 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02027 | hp2 | a0001 | c0001 | t0006 | g0328 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02055 | hp1 | a0001 | c0001 | t0021 | g0198 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02055 | hp2 | a0001 | c0001 | t0022 | g0179 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02056 | hp2 | a0002 | c0004 | t0001 | g0227 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02071 | hp1 | a0003 | c0003 | t0052 | g0349 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02074 | hp1 | a0002 | c0004 | t0001 | g0234 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02080 | hp2 | a0002 | c0002 | t0007 | g0128 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02083 | hp1 | a0001 | c0008 | t0001 | g0046 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0222 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02132 | hp1 | a0003 | c0003 | t0003 | g0078 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02132 | hp2 | a0002 | c0002 | t0007 | g0144 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02135 | hp1 | a0001 | c0008 | t0001 | g0045 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0363 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02145 | hp2 | a0002 | c0005 | t0004 | g0361 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0347 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02148 | hp2 | a0001 | c0001 | t0011 | g0097 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | CDX | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0104 | EAS | CDX | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02257 | hp1 | a0001 | c0001 | t0028 | g0181 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02258 | hp2 | a0001 | c0001 | t0021 | g0212 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02280 | hp1 | a0002 | c0005 | t0004 | g0362 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0156 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02293 | hp1 | a0001 | c0001 | t0011 | g0085 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0343 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02523 | hp1 | a0002 | c0002 | t0003 | g0121 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | KHV | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0357 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02572 | hp2 | a0001 | c0001 | t0044 | g0317 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0359 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02615 | hp1 | a0001 | c0001 | t0015 | g0367 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02615 | hp2 | a0001 | c0007 | t0013 | g0243 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02622 | hp1 | a0002 | c0002 | t0004 | g0295 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02622 | hp2 | a0001 | c0001 | t0034 | g0228 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0319 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02647 | hp1 | a0002 | c0002 | t0004 | g0182 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02647 | hp2 | a0001 | c0001 | t0024 | g0180 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0114 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02683 | hp2 | a0002 | c0002 | t0004 | g0239 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02717 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02717 | hp2 | a0002 | c0002 | t0018 | g0354 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02723 | hp1 | a0001 | c0001 | t0020 | g0024 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02723 | hp2 | a0002 | c0002 | t0014 | g0279 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0258 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02738 | hp1 | a0002 | c0002 | t0005 | g0322 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02738 | hp2 | a0003 | c0003 | t0035 | g0321 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02809 | hp1 | a0001 | c0001 | t0022 | g0051 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02809 | hp2 | a0002 | c0002 | t0004 | g0176 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02818 | hp1 | a0001 | c0001 | t0028 | g0316 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02818 | hp2 | a0002 | c0002 | t0045 | g0037 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02886 | hp1 | a0001 | c0001 | t0051 | g0177 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02886 | hp2 | a0002 | c0002 | t0046 | g0188 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02895 | hp1 | a0002 | c0002 | t0026 | g0025 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02895 | hp2 | a0001 | c0001 | t0029 | g0193 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0189 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0190 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02897 | hp2 | a0001 | c0001 | t0029 | g0192 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02922 | hp1 | a0001 | c0001 | t0036 | g0007 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02922 | hp2 | a0002 | c0002 | t0013 | g0016 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02965 | hp1 | a0001 | c0001 | t0016 | g0178 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0315 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02970 | hp1 | a0002 | c0002 | t0060 | g0138 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02976 | hp1 | a0002 | c0002 | t0026 | g0299 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02976 | hp2 | a0001 | c0001 | t0015 | g0370 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0364 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0122 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03041 | hp1 | a0001 | c0001 | t0016 | g0355 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03041 | hp2 | a0002 | c0002 | t0004 | g0318 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03098 | hp1 | a0001 | c0001 | t0018 | g0352 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0365 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03139 | hp1 | a0002 | c0002 | t0026 | g0281 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0214 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03195 | hp1 | a0001 | c0001 | t0015 | g0368 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03195 | hp2 | a0009 | c0015 | t0019 | g0004 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03209 | hp1 | a0001 | c0001 | t0057 | g0213 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0174 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03225 | hp1 | a0002 | c0004 | t0053 | g0019 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03225 | hp2 | a0001 | c0001 | t0014 | g0369 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03239 | hp1 | a0002 | c0002 | t0074 | g0371 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03239 | hp2 | a0002 | c0004 | t0017 | g0217 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03453 | hp1 | a0002 | c0002 | t0015 | g0385 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03453 | hp2 | a0001 | c0001 | t0076 | g0386 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03486 | hp1 | a0012 | c0014 | t0019 | g0125 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0324 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03491 | hp1 | a0001 | c0001 | t0027 | g0022 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03492 | hp2 | a0001 | c0001 | t0027 | g0023 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0184 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0387 | AFR | ESN | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03540 | hp2 | a0002 | c0002 | t0013 | g0001 | AFR | GWD | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03579 | hp1 | a0001 | c0001 | t0059 | g0332 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03579 | hp2 | a0001 | c0007 | t0013 | g0249 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03669 | hp1 | a0001 | c0001 | t0010 | g0127 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03669 | hp2 | a0001 | c0001 | t0058 | g0106 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03688 | hp1 | a0001 | c0001 | t0039 | g0109 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03688 | hp2 | a0003 | c0003 | t0005 | g0242 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03704 | hp2 | a0001 | c0001 | t0040 | g0255 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0287 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03710 | hp2 | a0001 | c0001 | t0017 | g0302 | SAS | PJL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0313 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03834 | hp1 | a0002 | c0002 | t0025 | g0139 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03834 | hp2 | a0002 | c0002 | t0005 | g0312 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03927 | hp1 | a0001 | c0001 | t0070 | g0119 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03927 | hp2 | a0001 | c0001 | t0063 | g0133 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0301 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03942 | hp2 | a0003 | c0003 | t0032 | g0241 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG04115 | hp2 | a0001 | c0001 | t0025 | g0219 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0238 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | BEB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG04199 | hp2 | a0001 | c0001 | t0048 | g0259 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG04204 | hp2 | a0002 | c0004 | t0005 | g0272 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG04228 | hp1 | a0002 | c0002 | t0073 | g0160 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | STU | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18522 | hp1 | a0001 | c0001 | t0019 | g0388 | AFR | YRI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18522 | hp2 | a0001 | c0001 | t0049 | g0010 | AFR | YRI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18612 | hp2 | a0002 | c0002 | t0006 | g0033 | EAS | CHB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | CHB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18747 | hp2 | a0001 | c0001 | t0033 | g0191 | EAS | CHB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0331 | AFR | YRI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18906 | hp2 | a0002 | c0002 | t0018 | g0038 | AFR | YRI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18940 | hp1 | a0002 | c0002 | t0007 | g0360 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18940 | hp2 | a0001 | c0001 | t0069 | g0304 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18941 | hp1 | a0004 | c0016 | t0007 | g0135 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18941 | hp2 | a0001 | c0001 | t0012 | g0147 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18943 | hp1 | a0002 | c0002 | t0003 | g0091 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18945 | hp1 | a0002 | c0002 | t0012 | g0384 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18946 | hp2 | a0001 | c0001 | t0008 | g0047 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18947 | hp1 | a0001 | c0001 | t0011 | g0075 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18947 | hp2 | a0001 | c0001 | t0008 | g0306 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18949 | hp1 | a0002 | c0002 | t0007 | g0027 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18950 | hp2 | a0002 | c0002 | t0061 | g0252 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18951 | hp1 | a0003 | c0003 | t0006 | g0166 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18951 | hp2 | a0002 | c0002 | t0007 | g0005 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18953 | hp1 | a0002 | c0002 | t0005 | g0143 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18954 | hp1 | a0001 | c0001 | t0008 | g0067 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0168 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18956 | hp2 | a0003 | c0003 | t0062 | g0265 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18957 | hp1 | a0004 | c0006 | t0001 | g0136 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18957 | hp2 | a0001 | c0001 | t0008 | g0090 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18959 | hp1 | a0001 | c0001 | t0012 | g0032 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18959 | hp2 | a0002 | c0002 | t0007 | g0005 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18960 | hp2 | a0001 | c0001 | t0008 | g0084 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18962 | hp1 | a0002 | c0004 | t0001 | g0044 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18964 | hp1 | a0002 | c0002 | t0006 | g0132 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18970 | hp2 | a0002 | c0002 | t0007 | g0095 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18971 | hp2 | a0002 | c0002 | t0006 | g0254 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0374 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18977 | hp2 | a0002 | c0002 | t0005 | g0131 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18978 | hp1 | a0002 | c0002 | t0007 | g0140 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18979 | hp1 | a0003 | c0003 | t0006 | g0232 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18980 | hp2 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18981 | hp1 | a0001 | c0001 | t0008 | g0063 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18981 | hp2 | a0003 | c0003 | t0008 | g0264 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18984 | hp1 | a0002 | c0004 | t0001 | g0247 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18984 | hp2 | a0001 | c0001 | t0071 | g0297 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18985 | hp1 | a0002 | c0002 | t0007 | g0053 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18986 | hp1 | a0002 | c0004 | t0005 | g0246 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18990 | hp1 | a0001 | c0001 | t0008 | g0129 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18990 | hp2 | a0001 | c0001 | t0011 | g0065 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18991 | hp1 | a0001 | c0001 | t0008 | g0105 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18993 | hp1 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18994 | hp2 | a0002 | c0002 | t0005 | g0130 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19005 | hp1 | a0002 | c0002 | t0075 | g0149 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19005 | hp2 | a0003 | c0003 | t0006 | g0270 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19007 | hp2 | a0002 | c0002 | t0066 | g0167 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19009 | hp2 | a0001 | c0001 | t0008 | g0058 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19012 | hp1 | a0004 | c0006 | t0007 | g0137 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19012 | hp2 | a0002 | c0002 | t0007 | g0100 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19030 | hp1 | a0010 | c0012 | t0050 | g0248 | AFR | LWK | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19030 | hp2 | a0001 | c0001 | t0019 | g0389 | AFR | LWK | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19043 | hp1 | a0002 | c0002 | t0038 | g0194 | AFR | LWK | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | LWK | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19054 | hp1 | a0002 | c0002 | t0012 | g0237 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0383 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19057 | hp1 | a0001 | c0001 | t0008 | g0103 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19057 | hp2 | a0001 | c0001 | t0012 | g0164 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19063 | hp1 | a0001 | c0001 | t0008 | g0089 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0382 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19064 | hp2 | a0002 | c0002 | t0007 | g0141 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19065 | hp1 | a0003 | c0003 | t0008 | g0263 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0092 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19078 | hp1 | a0001 | c0001 | t0012 | g0145 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19078 | hp2 | a0001 | c0001 | t0008 | g0093 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19079 | hp1 | a0001 | c0001 | t0012 | g0148 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19079 | hp2 | a0003 | c0003 | t0068 | g0226 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19081 | hp1 | a0001 | c0001 | t0006 | g0261 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19081 | hp2 | a0003 | c0003 | t0005 | g0054 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19082 | hp1 | a0007 | c0009 | t0001 | g0055 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19085 | hp1 | a0005 | c0017 | t0011 | g0171 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19087 | hp2 | a0001 | c0001 | t0033 | g0253 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19088 | hp1 | a0004 | c0006 | t0001 | g0134 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19088 | hp2 | a0002 | c0002 | t0006 | g0250 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19090 | hp2 | a0001 | c0001 | t0065 | g0064 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19240 | hp1 | a0002 | c0005 | t0004 | g0004 | AFR | YRI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | YRI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA20129 | hp1 | a0001 | c0001 | t0037 | g0014 | AFR | ASW | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA20129 | hp2 | a0002 | c0002 | t0013 | g0013 | AFR | ASW | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0381 | EUR | TSI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0298 | EUR | TSI | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0350 | SAS | GIH | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA20905 | hp2 | a0001 | c0001 | t0042 | g0333 | SAS | GIH | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01123 | hp1 | a0001 | c0001 | t0010 | g0294 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG01123 | hp2 | a0001 | c0001 | t0025 | g0205 | AMR | CLM | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0175 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02109 | hp2 | a0002 | c0002 | t0018 | g0183 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0330 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG02559 | hp2 | a0002 | c0002 | t0013 | g0280 | AFR | ACB | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03471 | hp1 | a0001 | c0001 | t0024 | g0015 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG06807 | hp1 | a0002 | c0002 | t0021 | g0034 | AFR | USA | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| HG06807 | hp2 | a0001 | c0001 | t0016 | g0187 | AFR | USA | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18955 | hp1 | a0001 | c0001 | t0007 | g0200 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA20300 | hp1 | a0001 | c0001 | t0056 | g0358 | AFR | USA | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0229 | AFR | USA | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA21309 | hp1 | a0002 | c0002 | t0013 | g0001 | AFR | LWK | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| NA21309 | hp2 | a0002 | c0002 | t0047 | g0309 | AFR | LWK | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0087 | REF | REF | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| homoSapiens_grch38 | hp1 | a0002 | c0004 | t0054 | g0311 | REF | REF | TSPAN11_chr12_30921748_31001599 | TSPAN11 | chr12 | 30921748 | 31001599 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:30954007
|
A | C | 3 | a0003a0004a0005 | 22 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(19): Show |
missense_variant | MODERATE | c.16A>C | p.Thr6Pro | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/8 | 76/5506 | 16/762 | 6/253 | chr12 | 30954007 | ||
| chr12:30963892
|
G | T | 1 | a0006 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.151G>T | p.Val51Phe | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/8 | 211/5506 | 151/762 | 51/253 | chr12 | 30963892 | ||
| chr12:30978613
|
T | C | 1 | a0012 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.329T>C | p.Leu110Pro | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/8 | 389/5506 | 329/762 | 110/253 | chr12 | 30978613 | ||
| chr12:30979597
|
G | A | 1 | a0007 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.383G>A | p.Arg128Gln | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/8 | 443/5506 | 383/762 | 128/253 | chr12 | 30979597 | ||
| chr12:30982598
|
G | A | 1 | a0011 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.523G>A | p.Ala175Thr | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/8 | 583/5506 | 523/762 | 175/253 | chr12 | 30982598 | ||
| chr12:30982644
|
T | C | 8 | a0001a0003a0005others(5): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
missense_variant | MODERATE | c.569T>C | p.Val190Ala | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/8 | 629/5506 | 569/762 | 190/253 | chr12 | 30982644 | ||
| chr12:30982680
|
A | G | 1 | a0005 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.605A>G | p.Tyr202Cys | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/8 | 665/5506 | 605/762 | 202/253 | chr12 | 30982680 | ||
| chr12:30983100
|
G | A | 1 | a0008 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.652G>A | p.Asp218Asn | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/8 | 712/5506 | 652/762 | 218/253 | chr12 | 30983100 | ||
| chr12:30991875
|
C | A | 1 | a0009 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.722C>A | p.Thr241Asn | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 782/5506 | 722/762 | 241/253 | chr12 | 30991875 | ||
| chr12:30991902
|
G | A | 1 | a0010 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.749G>A | p.Arg250Gln | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 809/5506 | 749/762 | 250/253 | chr12 | 30991902 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:30954018
|
C | T | 1 | a0001c0008 | 2 | HG02083.hp1 HG02135.hp1 |
synonymous_variant | LOW | c.27C>T | p.Asp9Asp | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/8 | 87/5506 | 27/762 | 9/253 | chr12 | 30954018 | ||
| chr12:30963888
|
C | G | 3 | a0002c0005a0009c0015a0012c0014 | 5 | HG02145.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
synonymous_variant | LOW | c.147C>G | p.Leu49Leu | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/8 | 207/5506 | 147/762 | 49/253 | chr12 | 30963888 | ||
| chr12:30982543
|
T | C | 14 | a0001c0001a0001c0007a0001c0008others(11): Show | 375 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(372): Show |
synonymous_variant | LOW | c.468T>C | p.Cys156Cys | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/8 | 528/5506 | 468/762 | 156/253 | chr12 | 30982543 | ||
| chr12:30982579
|
G | A | 1 | a0004c0016 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.504G>A | p.Thr168Thr | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/8 | 564/5506 | 504/762 | 168/253 | chr12 | 30982579 | ||
| chr12:30982651
|
C | T | 1 | a0001c0007 | 2 | HG02615.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.576C>T | p.Cys192Cys | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/8 | 636/5506 | 576/762 | 192/253 | chr12 | 30982651 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:30991949
|
A | G | 74 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(71): Show | 263 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*34A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 34 | chr12 | 30991949 | |||||
| chr12:30991971
|
A | G | 2 | a0001c0001t0056a0001c0001t0057 | 2 | HG03209.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*56A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 56 | chr12 | 30991971 | |||||
| chr12:30992037
|
A | G | 1 | a0001c0001t0055 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 122 | chr12 | 30992037 | |||||
| chr12:30992075
|
T | TCTA | 114 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(111): Show | 387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
3_prime_UTR_variant | MODIFIER | c.*162_*163insACT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 163 | INFO_REALIGN_3_PRIME | chr12 | 30992075 | ||||
| chr12:30992094
|
A | G | 68 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(65): Show | 251 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*179A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 179 | chr12 | 30992094 | |||||
| chr12:30992101
|
C | T | 3 | a0001c0001t0016a0001c0001t0056a0001c0001t0057 | 7 | HG02965.hp1 HG03041.hp1 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*186C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 186 | chr12 | 30992101 | |||||
| chr12:30992149
|
G | A | 10 | a0001c0001t0006a0001c0001t0028a0001c0001t0029others(7): Show | 28 | HG00558.hp2 HG00621.hp1 HG01070.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*234G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 234 | chr12 | 30992149 | |||||
| chr12:30992151
|
G | A | 1 | a0003c0003t0035 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 236 | chr12 | 30992151 | |||||
| chr12:30992234
|
C | A | 3 | a0001c0001t0011a0005c0017t0011a0006c0013t0011 | 9 | HG01952.hp2 HG01975.hp1 HG01978.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*319C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 319 | chr12 | 30992234 | |||||
| chr12:30992270
|
G | C | 3 | a0001c0001t0016a0001c0001t0056a0001c0001t0057 | 7 | HG02965.hp1 HG03041.hp1 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*355G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 355 | chr12 | 30992270 | |||||
| chr12:30992370
|
G | C | 12 | a0001c0001t0010a0001c0001t0014a0001c0001t0018others(9): Show | 28 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*455G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 455 | chr12 | 30992370 | |||||
| chr12:30992590
|
G | A | 1 | a0001c0001t0037 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*675G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 675 | chr12 | 30992590 | |||||
| chr12:30992698
|
G | A | 3 | a0001c0001t0008a0001c0001t0065a0003c0003t0008 | 15 | NA18946.hp2 NA18947.hp2 NA18954.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*783G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 783 | chr12 | 30992698 | |||||
| chr12:30992739
|
A | G | 11 | a0001c0001t0007a0001c0001t0018a0001c0001t0034others(8): Show | 31 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*824A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 824 | chr12 | 30992739 | |||||
| chr12:30992791
|
A | C | 46 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(43): Show | 161 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*876A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 876 | chr12 | 30992791 | |||||
| chr12:30992981
|
A | T | 12 | a0001c0001t0004a0001c0001t0048a0001c0001t0049others(9): Show | 31 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1066A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1066 | chr12 | 30992981 | |||||
| chr12:30992989
|
G | A | 3 | a0001c0001t0020a0001c0001t0036a0002c0002t0038 | 5 | HG01167.hp2 HG01169.hp2 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1074G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1074 | chr12 | 30992989 | |||||
| chr12:30993113
|
A | AC | 14 | a0001c0001t0010a0001c0001t0014a0001c0001t0018others(11): Show | 32 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1205dupC | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1206 | INFO_REALIGN_3_PRIME | chr12 | 30993113 | ||||
| chr12:30993125
|
G | A | 56 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(53): Show | 212 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*1210G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1210 | chr12 | 30993125 | |||||
| chr12:30993204
|
C | T | 1 | a0001c0001t0033 | 2 | NA18747.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1289C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1289 | chr12 | 30993204 | |||||
| chr12:30993266
|
C | G | 3 | a0001c0001t0015a0001c0001t0044a0002c0002t0015 | 6 | HG01192.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1351C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1351 | chr12 | 30993266 | |||||
| chr12:30993522
|
T | C | 1 | a0002c0002t0066 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1607T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1607 | chr12 | 30993522 | |||||
| chr12:30993599
|
G | A | 10 | a0001c0001t0004a0001c0001t0048a0001c0001t0049others(7): Show | 29 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1684G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1684 | chr12 | 30993599 | |||||
| chr12:30993700
|
A | G | 60 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(57): Show | 219 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1785A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1785 | chr12 | 30993700 | |||||
| chr12:30993758
|
C | T | 1 | a0001c0001t0049 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1843C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1843 | chr12 | 30993758 | |||||
| chr12:30993782
|
G | A | 1 | a0001c0001t0039 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1867G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1867 | chr12 | 30993782 | |||||
| chr12:30993821
|
C | T | 8 | a0001c0001t0007a0001c0001t0034a0002c0002t0007others(5): Show | 25 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1906C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1906 | chr12 | 30993821 | |||||
| chr12:30993822
|
G | A | 1 | a0001c0001t0040 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1907G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 1907 | chr12 | 30993822 | |||||
| chr12:30993939
|
G | A | 56 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(53): Show | 212 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*2024G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2024 | chr12 | 30993939 | |||||
| chr12:30994013
|
A | C | 2 | a0001c0001t0056a0001c0001t0057 | 2 | HG03209.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2098A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2098 | chr12 | 30994013 | |||||
| chr12:30994200
|
G | T | 1 | a0003c0003t0062 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2285G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2285 | chr12 | 30994200 | |||||
| chr12:30994248
|
G | A | 1 | a0001c0001t0034 | 2 | HG01884.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2333G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2333 | chr12 | 30994248 | |||||
| chr12:30994294
|
A | G | 1 | a0002c0002t0073 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2379A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2379 | chr12 | 30994294 | |||||
| chr12:30994364
|
G | A | 1 | a0002c0002t0061 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2449G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2449 | chr12 | 30994364 | |||||
| chr12:30994477
|
C | T | 1 | a0001c0001t0048 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2562C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2562 | chr12 | 30994477 | |||||
| chr12:30994500
|
G | A | 91 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(88): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*2585G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2585 | chr12 | 30994500 | |||||
| chr12:30994506
|
G | A | 7 | a0001c0001t0005a0001c0001t0044a0001c0001t0070others(4): Show | 24 | HG01257.hp2 HG01258.hp2 HG01496.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2591G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2591 | chr12 | 30994506 | |||||
| chr12:30994540
|
G | T | 34 | a0001c0001t0002a0001c0001t0004a0001c0001t0015others(31): Show | 106 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*2625G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2625 | chr12 | 30994540 | |||||
| chr12:30994602
|
G | C | 1 | a0001c0001t0071 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2687G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2687 | chr12 | 30994602 | |||||
| chr12:30994677
|
C | T | 3 | a0001c0001t0036a0002c0002t0026a0002c0002t0038 | 5 | HG02895.hp1 HG02922.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2762C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 2762 | chr12 | 30994677 | |||||
| chr12:30994940
|
C | T | 4 | a0001c0001t0016a0001c0001t0018a0001c0001t0076others(1): Show | 11 | HG01891.hp2 HG02109.hp2 HG02717.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3025C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3025 | chr12 | 30994940 | |||||
| chr12:30994997
|
CAG | C | 5 | a0001c0001t0016a0001c0001t0018a0001c0001t0076others(2): Show | 12 | HG01891.hp2 HG02109.hp2 HG02717.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3083_*3084delAG | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3083 | chr12 | 30994997 | |||||
| chr12:30995252
|
G | A | 21 | a0001c0001t0001a0001c0001t0017a0001c0001t0019others(18): Show | 91 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*3337G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3337 | chr12 | 30995252 | |||||
| chr12:30995414
|
G | C | 1 | a0010c0012t0050 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3499G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3499 | chr12 | 30995414 | |||||
| chr12:30995446
|
A | C | 32 | a0001c0001t0001a0001c0001t0010a0001c0001t0017others(29): Show | 113 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3531A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3531 | chr12 | 30995446 | |||||
| chr12:30995480
|
C | T | 1 | a0001c0001t0070 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3565C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3565 | chr12 | 30995480 | |||||
| chr12:30995483
|
G | A | 2 | a0002c0002t0041a0010c0012t0050 | 2 | HG01884.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3568G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3568 | chr12 | 30995483 | |||||
| chr12:30995498
|
G | C | 1 | a0001c0001t0042 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3583G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3583 | chr12 | 30995498 | |||||
| chr12:30995700
|
C | T | 1 | a0010c0012t0050 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3785C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3785 | chr12 | 30995700 | |||||
| chr12:30995727
|
G | A | 82 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(79): Show | 275 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*3812G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3812 | chr12 | 30995727 | |||||
| chr12:30995740
|
G | A | 1 | a0010c0012t0050 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3825G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3825 | chr12 | 30995740 | |||||
| chr12:30995784
|
TACAA | T | 82 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(79): Show | 275 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*3873_*3876delAACA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3873 | INFO_REALIGN_3_PRIME | chr12 | 30995784 | ||||
| chr12:30995857
|
G | A | 83 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(80): Show | 276 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*3942G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3942 | chr12 | 30995857 | |||||
| chr12:30995867
|
C | T | 82 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(79): Show | 275 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*3952C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 3952 | chr12 | 30995867 | |||||
| chr12:30995921
|
C | A | 1 | a0001c0001t0043 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4006C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4006 | chr12 | 30995921 | |||||
| chr12:30995935
|
A | C | 2 | a0002c0002t0030a0002c0004t0030 | 2 | HG01070.hp1 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4020A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4020 | chr12 | 30995935 | |||||
| chr12:30995957
|
C | T | 1 | a0010c0012t0050 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4042C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4042 | chr12 | 30995957 | |||||
| chr12:30995983
|
G | C | 1 | a0001c0001t0016 | 5 | HG02965.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4068G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4068 | chr12 | 30995983 | |||||
| chr12:30996009
|
C | T | 4 | a0001c0001t0016a0001c0001t0018a0001c0001t0076others(1): Show | 11 | HG01891.hp2 HG02109.hp2 HG02717.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4094C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4094 | chr12 | 30996009 | |||||
| chr12:30996097
|
G | A | 1 | a0010c0012t0050 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4182G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4182 | chr12 | 30996097 | |||||
| chr12:30996274
|
T | G | 2 | a0001c0001t0022a0011c0010t0022 | 3 | HG01891.hp1 HG02055.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4359T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4359 | chr12 | 30996274 | |||||
| chr12:30996485
|
C | T | 1 | a0010c0012t0050 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4570C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 8/8 | 4570 | chr12 | 30996485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:30927105
|
G | C | 1 | a0001c0001t0004g0006 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-12+309G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927105 | ||||||
| chr12:30927131
|
C | T | 5 | a0001c0001t0014g0387a0001c0001t0019g0388a0001c0001t0019g0389others(2): Show | 5 | HG03453.hp1 HG03453.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+335C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927131 | ||||||
| chr12:30927393
|
G | T | 1 | a0002c0002t0012g0384 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-12+597G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927393 | ||||||
| chr12:30927460
|
T | C | 1 | a0001c0001t0036g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+664T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927460 | ||||||
| chr12:30927473
|
G | A | 18 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0014g0387others(15): Show | 19 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-12+677G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927473 | ||||||
| chr12:30927516
|
G | C | 2 | a0001c0001t0001g0020a0002c0002t0004g0021 | 2 | HG01106.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-12+720G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927516 | ||||||
| chr12:30927597
|
G | A | 2 | a0001c0001t0027g0022a0001c0001t0027g0023 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-12+801G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927597 | ||||||
| chr12:30927802
|
G | T | 1 | a0001c0001t0004g0006 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-12+1006G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927802 | ||||||
| chr12:30927923
|
T | A | 3 | a0001c0001t0014g0387a0001c0001t0076g0386a0002c0002t0015g0385 | 3 | HG03453.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-12+1127T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30927923 | ||||||
| chr12:30928005
|
C | T | 2 | a0001c0001t0001g0382a0001c0001t0003g0383 | 2 | NA19054.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-12+1209C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928005 | ||||||
| chr12:30928006
|
G | A | 2 | a0001c0001t0020g0024a0002c0002t0026g0025 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-12+1210G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928006 | ||||||
| chr12:30928019
|
G | A | 31 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0382others(28): Show | 31 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.-12+1223G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928019 | ||||||
| chr12:30928196
|
G | A | 71 | a0001c0001t0001g0056a0001c0001t0001g0080a0001c0001t0001g0086others(68): Show | 72 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.-12+1400G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928196 | ||||||
| chr12:30928301
|
G | A | 1 | a0002c0002t0014g0124 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-12+1505G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928301 | ||||||
| chr12:30928450
|
G | A | 1 | a0012c0014t0019g0125 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12+1654G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928450 | ||||||
| chr12:30928628
|
C | T | 1 | a0002c0002t0007g0005 | 2 | NA18951.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-12+1832C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928628 | ||||||
| chr12:30928734
|
A | G | 2 | a0001c0001t0002g0123a0001c0001t0005g0122 | 2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-12+1938A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928734 | ||||||
| chr12:30928794
|
A | G | 18 | a0001c0001t0002g0374a0001c0001t0002g0375a0001c0001t0002g0376others(15): Show | 18 | HG00438.hp1 HG01074.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+1998A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928794 | ||||||
| chr12:30928901
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-12+2105G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928901 | ||||||
| chr12:30928981
|
G | C | 1 | a0001c0001t0034g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-12+2185G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30928981 | ||||||
| chr12:30929098
|
C | G | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12+2302C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929098 | ||||||
| chr12:30929156
|
A | G | 5 | a0002c0005t0004g0004a0002c0005t0004g0361a0002c0005t0004g0362others(2): Show | 5 | HG02145.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+2360A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929156 | ||||||
| chr12:30929192
|
C | T | 1 | a0002c0002t0003g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-12+2396C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929192 | ||||||
| chr12:30929193
|
G | A | 18 | a0001c0001t0002g0374a0001c0001t0002g0375a0001c0001t0002g0376others(15): Show | 18 | HG00438.hp1 HG01074.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+2397G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929193 | ||||||
| chr12:30929265
|
C | T | 1 | a0002c0002t0007g0053 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+2469C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929265 | ||||||
| chr12:30929270
|
T | G | 1 | a0001c0001t0010g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-12+2474T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929270 | ||||||
| chr12:30929306
|
A | G | 6 | a0001c0001t0002g0376a0001c0001t0005g0377a0001c0001t0005g0378others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+2510A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929306 | ||||||
| chr12:30929339
|
T | C | 61 | a0001c0001t0001g0146a0001c0001t0001g0154a0001c0001t0001g0165others(58): Show | 62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-12+2543T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929339 | ||||||
| chr12:30929390
|
T | C | 61 | a0001c0001t0001g0146a0001c0001t0001g0154a0001c0001t0001g0165others(58): Show | 62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-12+2594T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929390 | ||||||
| chr12:30929420
|
G | T | 1 | a0002c0002t0007g0360 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-12+2624G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929420 | ||||||
| chr12:30929436
|
C | A | 1 | a0002c0002t0007g0128 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-12+2640C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929436 | ||||||
| chr12:30929646
|
A | G | 1 | a0002c0002t0002g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+2850A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929646 | ||||||
| chr12:30929667
|
T | C | 1 | a0011c0010t0022g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-12+2871T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929667 | ||||||
| chr12:30929819
|
A | G | 1 | a0001c0001t0002g0359 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-12+3023A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30929819 | ||||||
| chr12:30930022
|
A | T | 1 | a0001c0001t0056g0358 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-12+3226A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930022 | ||||||
| chr12:30930073
|
A | G | 1 | a0001c0001t0004g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-12+3277A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930073 | ||||||
| chr12:30930098
|
G | A | 55 | a0001c0001t0001g0146a0001c0001t0001g0154a0001c0001t0001g0165others(52): Show | 56 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-12+3302G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930098 | ||||||
| chr12:30930143
|
A | T | 1 | a0002c0002t0001g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-12+3347A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930143 | ||||||
| chr12:30930170
|
C | G | 6 | a0001c0001t0001g0351a0001c0001t0001g0353a0001c0001t0001g0356others(3): Show | 6 | HG02258.hp1 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+3374C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930170 | ||||||
| chr12:30930173
|
C | T | 1 | a0001c0001t0022g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-12+3377C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930173 | ||||||
| chr12:30930391
|
G | A | 3 | a0001c0001t0004g0186a0001c0001t0016g0187a0002c0002t0046g0188 | 3 | HG02886.hp2 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-12+3595G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930391 | ||||||
| chr12:30930590
|
C | A | 1 | a0007c0009t0001g0055 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-12+3794C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930590 | ||||||
| chr12:30930698
|
T | C | 2 | a0001c0001t0006g0189a0001c0001t0006g0190 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-12+3902T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930698 | ||||||
| chr12:30930711
|
G | A | 70 | a0001c0001t0001g0056a0001c0001t0001g0080a0001c0001t0001g0086others(67): Show | 71 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-12+3915G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930711 | ||||||
| chr12:30930760
|
C | A | 4 | a0001c0001t0029g0192a0001c0001t0029g0193a0002c0002t0038g0194others(1): Show | 4 | HG00738.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+3964C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930760 | ||||||
| chr12:30930826
|
TTTCTCCC others(21): Show |
T | 1 | a0001c0001t0003g0196 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-12+4031_-12+4058d others(30): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930826 | ||||||
| chr12:30930848
|
A | G | 61 | a0001c0001t0001g0146a0001c0001t0001g0154a0001c0001t0001g0165others(58): Show | 62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-12+4052A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930848 | ||||||
| chr12:30930852
|
G | A | 13 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0020g0017others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12+4056G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930852 | ||||||
| chr12:30930929
|
C | T | 55 | a0001c0001t0001g0146a0001c0001t0001g0154a0001c0001t0001g0165others(52): Show | 56 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-12+4133C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30930929 | ||||||
| chr12:30931088
|
A | G | 2 | a0001c0001t0002g0350a0002c0002t0001g0120 | 2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-12+4292A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931088 | ||||||
| chr12:30931105
|
C | G | 19 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG02165.hp2 HG02602.hp2 HG02683.hp1 others(16): Show |
intron_variant | MODIFIER | c.-12+4309C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931105 | ||||||
| chr12:30931109
|
T | C | 73 | a0001c0001t0001g0146a0001c0001t0001g0154a0001c0001t0001g0165others(70): Show | 74 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-12+4313T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931109 | ||||||
| chr12:30931121
|
C | T | 1 | a0003c0003t0052g0349 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-12+4325C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931121 | ||||||
| chr12:30931159
|
A | G | 56 | a0001c0001t0001g0146a0001c0001t0001g0154a0001c0001t0001g0165others(53): Show | 57 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-12+4363A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931159 | ||||||
| chr12:30931297
|
G | C | 18 | a0001c0001t0002g0374a0001c0001t0002g0375a0001c0001t0002g0376others(15): Show | 18 | HG00438.hp1 HG01074.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+4501G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931297 | ||||||
| chr12:30931311
|
G | A | 18 | a0001c0001t0002g0374a0001c0001t0002g0375a0001c0001t0002g0376others(15): Show | 18 | HG00438.hp1 HG01074.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12+4515G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931311 | ||||||
| chr12:30931498
|
T | TAA | 308 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(305): Show | 311 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-12+4703_-12+4704i others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931498 | |||||
| chr12:30931517
|
G | A | 56 | a0001c0001t0001g0146a0001c0001t0001g0154a0001c0001t0001g0165others(53): Show | 57 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-12+4721G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931517 | ||||||
| chr12:30931605
|
C | T | 1 | a0002c0002t0026g0281 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-12+4809C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931605 | ||||||
| chr12:30931606
|
G | A | 37 | a0001c0001t0001g0020a0001c0001t0001g0197a0001c0001t0001g0203others(34): Show | 37 | HG00280.hp2 HG00609.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.-12+4810G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931606 | ||||||
| chr12:30931614
|
T | C | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12+4818T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931614 | ||||||
| chr12:30931739
|
G | A | 6 | a0001c0001t0001g0056a0001c0001t0003g0057a0001c0001t0003g0059others(3): Show | 6 | HG00609.hp2 HG02040.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+4943G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931739 | ||||||
| chr12:30931761
|
T | A | 104 | a0001c0001t0001g0020a0001c0001t0001g0197a0001c0001t0001g0203others(101): Show | 104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.-12+4965T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931761 | ||||||
| chr12:30931828
|
C | T | 1 | a0001c0001t0006g0222 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-12+5032C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931828 | ||||||
| chr12:30931879
|
C | CAAAA | 45 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0382others(42): Show | 46 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-12+5100_-12+5103d others(6): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | |||||
| chr12:30931879
|
C | CAAAAA | 13 | a0001c0001t0002g0026a0001c0001t0002g0363a0001c0001t0004g0009others(10): Show | 13 | HG01192.hp1 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12+5099_-12+5103d others(7): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | |||||
| chr12:30931879
|
C | CAAAAAAA others(1): Show |
45 | a0001c0001t0001g0257a0001c0001t0001g0262a0001c0001t0001g0267others(42): Show | 45 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.-12+5096_-12+5103d others(10): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | |||||
| chr12:30931879
|
C | CAAAAAAA others(2): Show |
153 | a0001c0001t0001g0020a0001c0001t0001g0080a0001c0001t0001g0086others(150): Show | 155 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.-12+5095_-12+5103d others(11): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | |||||
| chr12:30931879
|
C | CAAAAAAA others(3): Show |
31 | a0001c0001t0001g0056a0001c0001t0001g0197a0001c0001t0002g0223others(28): Show | 31 | HG00423.hp2 HG01891.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.-12+5094_-12+5103d others(12): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | |||||
| chr12:30931879
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0008g0129 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-12+5093_-12+5103d others(13): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | |||||
| chr12:30931879
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0356 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-12+5092_-12+5103d others(14): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | |||||
| chr12:30931879
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0353a0001c0001t0016g0355a0002c0002t0018g0354 | 3 | HG02258.hp1 HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-12+5091_-12+5103d others(15): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | |||||
| chr12:30931879
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0351a0001c0001t0018g0352 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-12+5090_-12+5103d others(16): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | |||||
| chr12:30931879
|
CAAA | C | 6 | a0001c0001t0029g0192a0001c0001t0029g0193a0001c0001t0056g0358others(3): Show | 6 | HG00738.hp1 HG02559.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+5101_-12+5103d others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30931879 | |||||
| chr12:30931999
|
G | A | 1 | a0001c0001t0002g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-12+5203G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30931999 | ||||||
| chr12:30932237
|
T | C | 70 | a0001c0001t0001g0056a0001c0001t0001g0080a0001c0001t0001g0086others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-12+5441T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932237 | ||||||
| chr12:30932375
|
C | T | 1 | a0001c0001t0070g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-12+5579C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932375 | ||||||
| chr12:30932407
|
G | A | 66 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0382others(63): Show | 67 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.-12+5611G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932407 | ||||||
| chr12:30932465
|
C | T | 73 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(70): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-12+5669C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932465 | ||||||
| chr12:30932471
|
G | A | 162 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0080others(159): Show | 163 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.-12+5675G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932471 | ||||||
| chr12:30932503
|
A | G | 5 | a0001c0001t0022g0179a0001c0001t0024g0180a0001c0001t0028g0181others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+5707A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932503 | ||||||
| chr12:30932516
|
C | T | 2 | a0001c0001t0023g0336a0001c0001t0023g0337 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-12+5720C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932516 | ||||||
| chr12:30932561
|
G | T | 9 | a0001c0001t0006g0189a0001c0001t0006g0190a0001c0001t0016g0178others(6): Show | 9 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+5765G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932561 | ||||||
| chr12:30932616
|
G | A | 66 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0099others(63): Show | 66 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.-12+5820G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932616 | ||||||
| chr12:30932747
|
A | G | 1 | a0001c0001t0006g0173 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-12+5951A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30932747 | ||||||
| chr12:30933167
|
C | T | 10 | a0001c0001t0004g0006a0001c0001t0006g0189a0001c0001t0006g0190others(7): Show | 10 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+6371C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933167 | ||||||
| chr12:30933225
|
A | G | 19 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG02165.hp2 HG02602.hp2 HG02683.hp1 others(16): Show |
intron_variant | MODIFIER | c.-12+6429A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933225 | ||||||
| chr12:30933285
|
C | G | 1 | a0001c0001t0036g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+6489C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933285 | ||||||
| chr12:30933300
|
T | TGACATTA others(92): Show |
91 | a0001c0001t0001g0146a0001c0001t0001g0154a0001c0001t0001g0165others(88): Show | 92 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-12+6538_-12+6636d others(101): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30933300 | |||||
| chr12:30933519
|
G | T | 1 | a0001c0001t0019g0389 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-12+6723G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933519 | ||||||
| chr12:30933546
|
C | T | 38 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0002g0026others(35): Show | 38 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+6750C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933546 | ||||||
| chr12:30933620
|
C | A | 1 | a0002c0002t0025g0139 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-12+6824C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933620 | ||||||
| chr12:30933673
|
TTGCAGCT others(8): Show |
T | 1 | a0001c0001t0056g0358 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-12+6900_-12+6914d others(17): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30933673 | |||||
| chr12:30933732
|
C | T | 1 | a0001c0001t0005g0381 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-12+6936C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933732 | ||||||
| chr12:30933876
|
C | T | 1 | a0002c0002t0001g0039 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-12+7080C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933876 | ||||||
| chr12:30933949
|
C | A | 1 | a0001c0001t0016g0365 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-12+7153C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933949 | ||||||
| chr12:30933957
|
G | A | 260 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0080others(257): Show | 261 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.-12+7161G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30933957 | ||||||
| chr12:30934001
|
C | A | 2 | a0001c0001t0002g0286a0001c0001t0002g0287 | 2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-12+7205C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934001 | ||||||
| chr12:30934085
|
C | T | 1 | a0001c0001t0010g0335 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-12+7289C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934085 | ||||||
| chr12:30934165
|
G | A | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12+7369G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934165 | ||||||
| chr12:30934172
|
C | A | 8 | a0001c0001t0001g0203a0001c0001t0001g0351a0001c0001t0001g0353others(5): Show | 8 | HG02258.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+7376C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934172 | ||||||
| chr12:30934268
|
T | C | 10 | a0001c0001t0004g0006a0001c0001t0006g0189a0001c0001t0006g0190others(7): Show | 10 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+7472T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934268 | ||||||
| chr12:30934297
|
T | A | 1 | a0001c0001t0036g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+7501T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934297 | ||||||
| chr12:30934402
|
G | A | 52 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(49): Show | 53 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-12+7606G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934402 | ||||||
| chr12:30934422
|
T | A | 103 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0001g0165others(100): Show | 103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.-12+7626T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934422 | ||||||
| chr12:30934632
|
A | AT | 80 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0107others(77): Show | 80 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.-12+7851dupT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30934632 | |||||
| chr12:30934632
|
A | ATT | 6 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0005g0118others(3): Show | 6 | NA18967.hp1 NA18991.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+7850_-12+7851d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30934632 | |||||
| chr12:30934632
|
AT | A | 7 | a0001c0001t0002g0363a0001c0001t0003g0040a0001c0001t0004g0009others(4): Show | 7 | HG00408.hp1 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12+7851delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30934632 | |||||
| chr12:30934632
|
ATTT | A | 10 | a0001c0001t0004g0006a0001c0001t0006g0189a0001c0001t0006g0190others(7): Show | 10 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+7849_-12+7851d others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30934632 | |||||
| chr12:30934653
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-12+7857T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934653 | ||||||
| chr12:30934669
|
G | A | 3 | a0002c0002t0006g0250a0002c0002t0007g0251a0002c0002t0061g0252 | 3 | HG00673.hp2 NA18950.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-12+7873G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934669 | ||||||
| chr12:30934818
|
T | C | 1 | a0002c0002t0002g0174 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-12+8022T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934818 | ||||||
| chr12:30934823
|
A | G | 244 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0080others(241): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.-12+8027A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934823 | ||||||
| chr12:30934954
|
G | A | 1 | a0001c0001t0036g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+8158G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30934954 | ||||||
| chr12:30935052
|
C | G | 5 | a0002c0005t0004g0004a0002c0005t0004g0361a0002c0005t0004g0362others(2): Show | 5 | HG02145.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+8256C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935052 | ||||||
| chr12:30935138
|
C | T | 9 | a0001c0001t0006g0189a0001c0001t0006g0190a0001c0001t0016g0178others(6): Show | 9 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+8342C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935138 | ||||||
| chr12:30935198
|
G | T | 244 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0080others(241): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.-12+8402G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935198 | ||||||
| chr12:30935356
|
T | C | 2 | a0002c0002t0001g0066a0002c0002t0001g0070 | 2 | NA18991.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-12+8560T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935356 | ||||||
| chr12:30935373
|
G | GT | 29 | a0001c0001t0001g0327a0001c0001t0002g0282a0001c0001t0002g0287others(26): Show | 29 | HG00408.hp1 HG00621.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-12+8603dupT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30935373 | |||||
| chr12:30935373
|
GT | G | 251 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0056others(248): Show | 252 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.-12+8603delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30935373 | |||||
| chr12:30935381
|
T | G | 24 | a0001c0001t0001g0020a0001c0001t0001g0169a0001c0001t0002g0123others(21): Show | 24 | HG00438.hp1 HG00733.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12+8585T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935381 | ||||||
| chr12:30935382
|
T | G | 217 | a0001c0001t0001g0056a0001c0001t0001g0080a0001c0001t0001g0086others(214): Show | 217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.-12+8586T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935382 | ||||||
| chr12:30935383
|
T | G | 1 | a0002c0002t0002g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-12+8587T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935383 | ||||||
| chr12:30935422
|
C | A | 1 | a0001c0001t0004g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-12+8626C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935422 | ||||||
| chr12:30935558
|
A | G | 1 | a0001c0001t0014g0369 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-12+8762A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935558 | ||||||
| chr12:30935661
|
C | T | 2 | a0001c0001t0008g0129a0002c0002t0006g0132 | 2 | NA18964.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-12+8865C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935661 | ||||||
| chr12:30935717
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-12+8921T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935717 | ||||||
| chr12:30935920
|
G | T | 44 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(41): Show | 45 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-12+9124G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30935920 | ||||||
| chr12:30936160
|
C | T | 7 | a0001c0001t0029g0192a0001c0001t0029g0193a0001c0001t0056g0358others(4): Show | 7 | HG00738.hp1 HG01167.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+9364C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936160 | ||||||
| chr12:30936184
|
G | GCTTAATT others(14): Show |
12 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0029g0192others(9): Show | 12 | HG00738.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-12+9389_-12+9409d others(23): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30936184 | |||||
| chr12:30936405
|
G | A | 315 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(312): Show | 317 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.-12+9609G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936405 | ||||||
| chr12:30936603
|
T | A | 1 | a0001c0001t0002g0347 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-12+9807T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936603 | ||||||
| chr12:30936612
|
G | A | 3 | a0001c0001t0004g0186a0001c0001t0016g0187a0002c0002t0046g0188 | 3 | HG02886.hp2 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-12+9816G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936612 | ||||||
| chr12:30936648
|
C | T | 1 | a0001c0001t0016g0178 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12+9852C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936648 | ||||||
| chr12:30936668
|
C | T | 252 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0080others(249): Show | 252 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.-12+9872C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936668 | ||||||
| chr12:30936738
|
G | A | 251 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0080others(248): Show | 251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.-12+9942G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936738 | ||||||
| chr12:30936824
|
G | C | 3 | a0002c0002t0001g0062a0002c0002t0001g0071a0002c0002t0001g0072 | 3 | HG02056.hp1 NA18747.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-12+10028G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936824 | ||||||
| chr12:30936830
|
G | T | 1 | a0002c0002t0066g0167 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-12+10034G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936830 | ||||||
| chr12:30936843
|
G | A | 1 | a0001c0001t0003g0196 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-12+10047G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936843 | ||||||
| chr12:30936859
|
C | A | 1 | a0001c0001t0056g0358 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-12+10063C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936859 | ||||||
| chr12:30936942
|
C | T | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12+10146C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936942 | ||||||
| chr12:30936945
|
T | A | 1 | a0001c0001t0010g0319 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-12+10149T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30936945 | ||||||
| chr12:30937017
|
G | A | 1 | a0001c0001t0016g0365 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-12+10221G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937017 | ||||||
| chr12:30937117
|
A | G | 150 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0154others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-12+10321A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937117 | ||||||
| chr12:30937171
|
T | A | 244 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0080others(241): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.-12+10375T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937171 | ||||||
| chr12:30937182
|
G | T | 1 | a0002c0002t0013g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-12+10386G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937182 | ||||||
| chr12:30937348
|
C | G | 1 | a0001c0001t0032g0268 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-12+10552C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937348 | ||||||
| chr12:30937361
|
C | T | 21 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0001g0113others(18): Show | 21 | HG02015.hp2 HG02165.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+10565C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937361 | ||||||
| chr12:30937383
|
C | A | 1 | a0002c0002t0013g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12+10587C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937383 | ||||||
| chr12:30937432
|
G | T | 1 | a0001c0001t0002g0026 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-12+10636G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937432 | ||||||
| chr12:30937434
|
G | T | 1 | a0001c0001t0002g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-12+10638G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937434 | ||||||
| chr12:30937669
|
G | A | 1 | a0002c0002t0014g0279 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-12+10873G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937669 | ||||||
| chr12:30937683
|
C | A | 41 | a0001c0001t0001g0020a0001c0001t0001g0197a0001c0001t0002g0210others(38): Show | 41 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.-12+10887C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937683 | ||||||
| chr12:30937756
|
T | C | 73 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0099others(70): Show | 73 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.-12+10960T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937756 | ||||||
| chr12:30937821
|
T | C | 52 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0099others(49): Show | 52 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.-12+11025T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30937821 | ||||||
| chr12:30938036
|
A | G | 3 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276 | 3 | HG00639.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-12+11240A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938036 | ||||||
| chr12:30938098
|
T | C | 44 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(41): Show | 45 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-12+11302T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938098 | ||||||
| chr12:30938214
|
A | T | 1 | a0003c0003t0006g0166 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-12+11418A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938214 | ||||||
| chr12:30938334
|
C | A | 244 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0080others(241): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.-12+11538C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938334 | ||||||
| chr12:30938353
|
C | T | 7 | a0001c0001t0029g0192a0001c0001t0029g0193a0001c0001t0056g0358others(4): Show | 7 | HG00738.hp1 HG01167.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+11557C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938353 | ||||||
| chr12:30938727
|
C | T | 1 | a0001c0001t0036g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+11931C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938727 | ||||||
| chr12:30938748
|
G | C | 9 | a0001c0001t0006g0189a0001c0001t0006g0190a0001c0001t0016g0178others(6): Show | 9 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+11952G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938748 | ||||||
| chr12:30938991
|
G | T | 1 | a0001c0001t0001g0165 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-12+12195G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938991 | ||||||
| chr12:30938994
|
A | G | 244 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0080others(241): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.-12+12198A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30938994 | ||||||
| chr12:30939182
|
A | G | 3 | a0001c0001t0003g0094a0001c0001t0003g0098a0002c0002t0007g0095 | 3 | NA18970.hp2 NA18971.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-12+12386A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939182 | ||||||
| chr12:30939212
|
G | T | 7 | a0001c0001t0029g0192a0001c0001t0029g0193a0001c0001t0056g0358others(4): Show | 7 | HG00738.hp1 HG01167.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+12416G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939212 | ||||||
| chr12:30939238
|
C | CA | 153 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0112others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-12+12458dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30939238 | |||||
| chr12:30939238
|
C | CAA | 84 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0099others(81): Show | 84 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-12+12457_-12+1245 others(6): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30939238 | |||||
| chr12:30939238
|
C | CAAAAA | 11 | a0001c0001t0001g0203a0001c0001t0001g0351a0001c0001t0001g0353others(8): Show | 11 | HG02145.hp1 HG02258.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12+12454_-12+1245 others(9): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30939238 | |||||
| chr12:30939238
|
C | CAAAAAA | 32 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0002g0026others(29): Show | 33 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.-12+12453_-12+1245 others(10): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30939238 | |||||
| chr12:30939238
|
C | CAAAAAAA | 10 | a0001c0001t0001g0146a0001c0001t0012g0145a0001c0001t0015g0366others(7): Show | 10 | HG01192.hp1 HG02135.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+12452_-12+1245 others(11): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30939238 | |||||
| chr12:30939378
|
TG | T | 3 | a0001c0001t0001g0235a0002c0002t0001g0236a0002c0002t0012g0237 | 3 | NA18945.hp2 NA18998.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-12+12585delG | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30939378 | |||||
| chr12:30939380
|
G | C | 3 | a0001c0001t0001g0235a0002c0002t0001g0236a0002c0002t0012g0237 | 3 | NA18945.hp2 NA18998.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-12+12584G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939380 | ||||||
| chr12:30939440
|
T | C | 53 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(50): Show | 54 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-12+12644T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939440 | ||||||
| chr12:30939476
|
C | T | 10 | a0001c0001t0004g0006a0001c0001t0006g0189a0001c0001t0006g0190others(7): Show | 10 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+12680C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939476 | ||||||
| chr12:30939536
|
T | C | 73 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0099others(70): Show | 73 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.-12+12740T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939536 | ||||||
| chr12:30939546
|
C | G | 1 | a0002c0002t0003g0091 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-12+12750C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939546 | ||||||
| chr12:30939570
|
T | G | 53 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(50): Show | 54 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-12+12774T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939570 | ||||||
| chr12:30939617
|
A | G | 297 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(294): Show | 298 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.-12+12821A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939617 | ||||||
| chr12:30939722
|
G | A | 1 | a0002c0002t0074g0371 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-12+12926G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939722 | ||||||
| chr12:30939762
|
A | G | 1 | a0001c0001t0056g0358 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-12+12966A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939762 | ||||||
| chr12:30939839
|
A | C | 53 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(50): Show | 54 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-12+13043A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939839 | ||||||
| chr12:30939854
|
C | T | 1 | a0002c0002t0004g0182 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-12+13058C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939854 | ||||||
| chr12:30939859
|
A | G | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12+13063A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939859 | ||||||
| chr12:30939866
|
T | G | 1 | a0001c0001t0036g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+13070T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939866 | ||||||
| chr12:30939894
|
G | T | 1 | a0002c0002t0004g0318 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-12+13098G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939894 | ||||||
| chr12:30939963
|
G | A | 143 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0154others(140): Show | 143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.-12+13167G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30939963 | ||||||
| chr12:30940032
|
G | A | 144 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0154others(141): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-12+13236G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940032 | ||||||
| chr12:30940135
|
G | A | 1 | a0001c0001t0037g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-12+13339G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940135 | ||||||
| chr12:30940160
|
G | A | 15 | a0001c0001t0004g0006a0001c0001t0006g0189a0001c0001t0006g0190others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+13364G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940160 | ||||||
| chr12:30940161
|
C | A | 15 | a0001c0001t0004g0006a0001c0001t0006g0189a0001c0001t0006g0190others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+13365C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940161 | ||||||
| chr12:30940298
|
A | G | 297 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(294): Show | 298 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.-12+13502A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940298 | ||||||
| chr12:30940314
|
A | C | 1 | a0004c0006t0007g0137 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-12+13518A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940314 | ||||||
| chr12:30940333
|
A | G | 3 | a0001c0001t0005g0377a0001c0001t0005g0378a0002c0002t0004g0379 | 3 | HG01257.hp2 HG01258.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-12+13537A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940333 | ||||||
| chr12:30940337
|
G | A | 1 | a0001c0001t0024g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-12+13541G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940337 | ||||||
| chr12:30940355
|
A | G | 1 | a0002c0002t0018g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-12+13559A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940355 | ||||||
| chr12:30940482
|
GAGAAATA others(3): Show |
G | 1 | a0001c0001t0008g0090 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-11-13495_-11-1348 others(14): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30940482 | |||||
| chr12:30940511
|
G | A | 1 | a0002c0004t0017g0152 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-11-13470G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940511 | ||||||
| chr12:30940600
|
G | T | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-11-13381G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940600 | ||||||
| chr12:30940702
|
C | T | 7 | a0001c0001t0029g0192a0001c0001t0029g0193a0001c0001t0056g0358others(4): Show | 7 | HG00738.hp1 HG01167.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-13279C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940702 | ||||||
| chr12:30940739
|
G | T | 1 | a0001c0001t0014g0387 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-11-13242G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940739 | ||||||
| chr12:30940837
|
C | T | 1 | a0001c0001t0036g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11-13144C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940837 | ||||||
| chr12:30940958
|
C | G | 1 | a0001c0001t0001g0165 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-11-13023C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30940958 | ||||||
| chr12:30941039
|
G | A | 44 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(41): Show | 45 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11-12942G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941039 | ||||||
| chr12:30941283
|
G | T | 1 | a0001c0001t0008g0089 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-11-12698G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941283 | ||||||
| chr12:30941356
|
A | G | 1 | a0001c0001t0005g0278 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-11-12625A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941356 | ||||||
| chr12:30941428
|
C | T | 144 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0154others(141): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-11-12553C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941428 | ||||||
| chr12:30941519
|
G | C | 6 | a0001c0001t0002g0210a0001c0001t0002g0211a0001c0001t0010g0209others(3): Show | 6 | HG01243.hp1 HG01928.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-12462G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941519 | ||||||
| chr12:30941626
|
G | T | 20 | a0001c0001t0002g0210a0001c0001t0002g0211a0001c0001t0002g0220others(17): Show | 20 | HG00280.hp2 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.-11-12355G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941626 | ||||||
| chr12:30941751
|
G | A | 44 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(41): Show | 45 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11-12230G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941751 | ||||||
| chr12:30941939
|
C | T | 2 | a0001c0001t0006g0222a0001c0001t0007g0200 | 2 | HG02083.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-11-12042C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30941939 | ||||||
| chr12:30942038
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0021g0212 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-11-11943G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942038 | ||||||
| chr12:30942102
|
G | A | 296 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(293): Show | 297 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.-11-11879G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942102 | ||||||
| chr12:30942110
|
C | T | 1 | a0002c0002t0004g0318 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-11-11871C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942110 | ||||||
| chr12:30942307
|
A | G | 64 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(61): Show | 66 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11-11674A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942307 | ||||||
| chr12:30942572
|
C | A | 1 | a0001c0001t0004g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11-11409C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942572 | ||||||
| chr12:30942689
|
T | C | 1 | a0002c0002t0013g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-11-11292T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942689 | ||||||
| chr12:30942727
|
T | TA | 278 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(275): Show | 279 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.-11-11239dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30942727 | |||||
| chr12:30942727
|
T | TAA | 23 | a0001c0001t0001g0203a0001c0001t0001g0351a0001c0001t0001g0353others(20): Show | 24 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.-11-11240_-11-1123 others(6): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30942727 | |||||
| chr12:30942832
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-11-11149C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942832 | ||||||
| chr12:30942847
|
T | C | 64 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(61): Show | 66 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11-11134T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942847 | ||||||
| chr12:30942890
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-11-11091A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942890 | ||||||
| chr12:30942949
|
G | A | 144 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0001g0154others(141): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-11-11032G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942949 | ||||||
| chr12:30942984
|
T | C | 1 | a0001c0001t0036g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11-10997T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30942984 | ||||||
| chr12:30943193
|
C | T | 1 | a0002c0002t0001g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-11-10788C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943193 | ||||||
| chr12:30943217
|
G | A | 309 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(306): Show | 311 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-11-10764G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943217 | ||||||
| chr12:30943369
|
C | A | 1 | a0001c0001t0006g0189 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-11-10612C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943369 | ||||||
| chr12:30943518
|
C | T | 2 | a0001c0007t0013g0243a0001c0007t0013g0249 | 2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-11-10463C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943518 | ||||||
| chr12:30943584
|
T | C | 1 | a0001c0001t0003g0266 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-11-10397T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943584 | ||||||
| chr12:30943585
|
G | T | 1 | a0001c0001t0003g0266 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-11-10396G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943585 | ||||||
| chr12:30943586
|
C | G | 1 | a0001c0001t0003g0266 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-11-10395C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943586 | ||||||
| chr12:30943795
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-11-10186G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943795 | ||||||
| chr12:30943835
|
C | T | 20 | a0001c0001t0001g0203a0001c0001t0001g0351a0001c0001t0001g0353others(17): Show | 21 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11-10146C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943835 | ||||||
| chr12:30943883
|
T | C | 1 | a0002c0002t0001g0293 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-11-10098T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30943883 | ||||||
| chr12:30944044
|
G | C | 3 | a0001c0001t0001g0235a0002c0002t0001g0236a0002c0002t0012g0237 | 3 | NA18945.hp2 NA18998.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-11-9937G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944044 | ||||||
| chr12:30944131
|
C | T | 12 | a0001c0001t0019g0388a0001c0001t0019g0389a0001c0001t0020g0017others(9): Show | 13 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11-9850C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944131 | ||||||
| chr12:30944195
|
C | G | 1 | a0001c0001t0036g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11-9786C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944195 | ||||||
| chr12:30944219
|
T | C | 2 | a0001c0001t0029g0192a0001c0001t0029g0193 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-11-9762T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944219 | ||||||
| chr12:30944451
|
A | G | 51 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0002g0077others(48): Show | 51 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.-11-9530A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944451 | ||||||
| chr12:30944572
|
C | T | 3 | a0001c0001t0003g0094a0001c0001t0003g0098a0002c0002t0007g0095 | 3 | NA18970.hp2 NA18971.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-11-9409C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944572 | ||||||
| chr12:30944577
|
AT | A | 63 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(60): Show | 65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-11-9403delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944577 | ||||||
| chr12:30944621
|
A | C | 6 | a0001c0001t0014g0369a0001c0001t0015g0366a0001c0001t0015g0367others(3): Show | 6 | HG01192.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-9360A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944621 | ||||||
| chr12:30944901
|
T | C | 3 | a0001c0001t0004g0186a0001c0001t0016g0187a0002c0002t0046g0188 | 3 | HG02886.hp2 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11-9080T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944901 | ||||||
| chr12:30944904
|
G | A | 1 | a0011c0010t0022g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11-9077G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944904 | ||||||
| chr12:30944937
|
A | T | 1 | a0002c0002t0004g0318 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-11-9044A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30944937 | ||||||
| chr12:30945069
|
G | C | 22 | a0001c0001t0001g0101a0001c0001t0001g0107a0001c0001t0001g0112others(19): Show | 22 | HG02015.hp2 HG02165.hp2 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.-11-8912G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945069 | ||||||
| chr12:30945087
|
C | A | 63 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(60): Show | 65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-11-8894C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945087 | ||||||
| chr12:30945306
|
A | G | 63 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(60): Show | 65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-11-8675A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945306 | ||||||
| chr12:30945447
|
A | G | 1 | a0002c0002t0002g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-11-8534A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945447 | ||||||
| chr12:30945534
|
C | T | 1 | a0001c0001t0011g0221 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-11-8447C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945534 | ||||||
| chr12:30945650
|
C | T | 63 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(60): Show | 65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-11-8331C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945650 | ||||||
| chr12:30945698
|
G | A | 1 | a0007c0009t0001g0055 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-11-8283G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945698 | ||||||
| chr12:30945813
|
TGTC | T | 3 | a0001c0001t0008g0067a0002c0002t0001g0068a0002c0002t0001g0069 | 3 | NA18954.hp1 NA18977.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-11-8165_-11-8163d others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30945813 | |||||
| chr12:30945834
|
T | C | 63 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(60): Show | 65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-11-8147T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945834 | ||||||
| chr12:30945869
|
C | A | 1 | a0001c0001t0040g0255 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-11-8112C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945869 | ||||||
| chr12:30945948
|
T | C | 1 | a0002c0002t0003g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-11-8033T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30945948 | ||||||
| chr12:30946028
|
G | A | 16 | a0001c0001t0002g0363a0001c0001t0004g0006a0001c0001t0006g0189others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-7953G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946028 | ||||||
| chr12:30946121
|
T | C | 1 | a0002c0002t0018g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-11-7860T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946121 | ||||||
| chr12:30946169
|
C | T | 7 | a0001c0001t0016g0331a0001c0001t0028g0316a0001c0001t0044g0317others(4): Show | 7 | HG02572.hp2 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-7812C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946169 | ||||||
| chr12:30946262
|
A | G | 7 | a0001c0001t0029g0192a0001c0001t0029g0193a0001c0001t0056g0358others(4): Show | 7 | HG00738.hp1 HG01167.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-7719A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946262 | ||||||
| chr12:30946406
|
G | A | 64 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(61): Show | 66 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11-7575G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946406 | ||||||
| chr12:30946529
|
A | G | 7 | a0001c0001t0016g0331a0001c0001t0028g0316a0001c0001t0044g0317others(4): Show | 7 | HG02572.hp2 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-7452A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946529 | ||||||
| chr12:30946602
|
A | G | 73 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0101others(70): Show | 73 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.-11-7379A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946602 | ||||||
| chr12:30946607
|
G | A | 1 | a0002c0002t0005g0322 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-11-7374G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946607 | ||||||
| chr12:30946833
|
G | A | 43 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(40): Show | 44 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.-11-7148G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946833 | ||||||
| chr12:30946853
|
C | T | 1 | a0001c0001t0002g0330 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-11-7128C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30946853 | ||||||
| chr12:30947107
|
C | T | 3 | a0001c0001t0014g0387a0001c0001t0076g0386a0002c0002t0015g0385 | 3 | HG03453.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-11-6874C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947107 | ||||||
| chr12:30947261
|
G | T | 7 | a0001c0001t0001g0203a0001c0001t0001g0351a0001c0001t0001g0353others(4): Show | 7 | HG02258.hp1 HG02717.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-6720G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947261 | ||||||
| chr12:30947541
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-11-6440C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947541 | ||||||
| chr12:30947572
|
G | T | 1 | a0001c0001t0004g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11-6409G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947572 | ||||||
| chr12:30947603
|
C | T | 1 | a0001c0001t0011g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-11-6378C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947603 | ||||||
| chr12:30947695
|
C | T | 58 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(55): Show | 60 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-11-6286C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947695 | ||||||
| chr12:30947730
|
C | G | 60 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(57): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.-11-6251C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947730 | ||||||
| chr12:30947802
|
C | T | 45 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(42): Show | 46 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-11-6179C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947802 | ||||||
| chr12:30947899
|
C | T | 5 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0034g0008others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-6082C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947899 | ||||||
| chr12:30947962
|
T | C | 9 | a0001c0001t0006g0189a0001c0001t0006g0190a0001c0001t0016g0178others(6): Show | 9 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11-6019T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30947962 | ||||||
| chr12:30948037
|
A | C | 1 | a0001c0001t0001g0356 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-11-5944A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948037 | ||||||
| chr12:30948067
|
C | T | 217 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(214): Show | 219 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-11-5914C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948067 | ||||||
| chr12:30948073
|
T | C | 58 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(55): Show | 60 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-11-5908T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948073 | ||||||
| chr12:30948105
|
C | T | 1 | a0002c0002t0046g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-11-5876C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948105 | ||||||
| chr12:30948400
|
A | G | 44 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(41): Show | 45 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11-5581A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948400 | ||||||
| chr12:30948406
|
C | G | 1 | a0001c0001t0003g0196 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-11-5575C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948406 | ||||||
| chr12:30948411
|
G | A | 1 | a0001c0001t0010g0335 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-11-5570G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948411 | ||||||
| chr12:30948558
|
G | A | 50 | a0001c0001t0001g0056a0001c0001t0001g0086a0001c0001t0001g0235others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.-11-5423G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30948558 | ||||||
| chr12:30949267
|
T | A | 12 | a0001c0001t0001g0356a0001c0001t0004g0357a0001c0001t0014g0369others(9): Show | 12 | HG01167.hp1 HG01192.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-4714T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949267 | ||||||
| chr12:30949297
|
C | G | 1 | a0002c0002t0005g0322 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-11-4684C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949297 | ||||||
| chr12:30949348
|
T | A | 83 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0001t0001g0165others(80): Show | 84 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-11-4633T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949348 | ||||||
| chr12:30949348
|
T | C | 210 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0080others(207): Show | 213 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.-11-4633T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949348 | ||||||
| chr12:30949431
|
G | A | 342 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0056others(339): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.-11-4550G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949431 | ||||||
| chr12:30949446
|
T | C | 20 | a0001c0001t0003g0040a0001c0001t0004g0186a0001c0001t0007g0092others(17): Show | 21 | HG00408.hp1 HG01943.hp1 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11-4535T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949446 | ||||||
| chr12:30949565
|
A | G | 1 | a0002c0002t0007g0005 | 2 | NA18951.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-11-4416A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949565 | ||||||
| chr12:30949581
|
G | A | 10 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0014g0369others(7): Show | 10 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11-4400G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949581 | ||||||
| chr12:30949748
|
G | C | 32 | a0001c0001t0001g0288a0001c0001t0002g0282a0001c0001t0002g0286others(29): Show | 33 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.-11-4233G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949748 | ||||||
| chr12:30949763
|
C | T | 1 | a0001c0001t0006g0285 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-11-4218C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949763 | ||||||
| chr12:30949816
|
C | T | 1 | a0003c0003t0001g0114 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-11-4165C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949816 | ||||||
| chr12:30949841
|
C | G | 69 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0086others(66): Show | 69 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-11-4140C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949841 | ||||||
| chr12:30949965
|
C | T | 7 | a0001c0001t0014g0387a0001c0001t0044g0317a0001c0001t0059g0332others(4): Show | 7 | HG02572.hp2 HG02886.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-4016C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30949965 | ||||||
| chr12:30950019
|
C | T | 12 | a0001c0001t0002g0220a0001c0001t0002g0363a0001c0001t0006g0222others(9): Show | 12 | HG00280.hp2 HG01069.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11-3962C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30950019 | ||||||
| chr12:30950068
|
G | C | 2 | a0001c0001t0001g0351a0001c0001t0001g0353 | 2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-11-3913G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30950068 | ||||||
| chr12:30950276
|
G | T | 1 | a0001c0001t0002g0347 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-11-3705G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30950276 | ||||||
| chr12:30950426
|
G | A | 6 | a0001c0001t0001g0099a0001c0001t0003g0289a0001c0001t0003g0320others(3): Show | 6 | HG00544.hp2 NA18967.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-3555G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30950426 | ||||||
| chr12:30950840
|
A | G | 6 | a0001c0001t0008g0063a0001c0001t0008g0089a0001c0001t0008g0093others(3): Show | 6 | NA18981.hp1 NA18990.hp1 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-3141A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30950840 | ||||||
| chr12:30950984
|
T | G | 1 | a0001c0001t0001g0244 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-11-2997T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30950984 | ||||||
| chr12:30951028
|
G | A | 92 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(89): Show | 92 | HG00558.hp1 HG00609.hp1 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.-11-2953G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30951028 | ||||||
| chr12:30951059
|
A | G | 1 | a0001c0001t0010g0050 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-11-2922A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30951059 | ||||||
| chr12:30951088
|
C | T | 20 | a0001c0001t0001g0146a0001c0001t0012g0032a0002c0002t0001g0035others(17): Show | 21 | HG00438.hp2 HG02080.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11-2893C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30951088 | ||||||
| chr12:30951089
|
G | A | 3 | a0001c0001t0056g0358a0002c0002t0013g0280a0002c0004t0014g0195 | 3 | HG00738.hp1 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-11-2892G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30951089 | ||||||
| chr12:30951553
|
G | A | 1 | a0006c0013t0011g0338 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-11-2428G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30951553 | ||||||
| chr12:30951679
|
A | AC | 3 | a0001c0001t0003g0289a0001c0001t0003g0320a0001c0001t0006g0284 | 3 | NA18985.hp2 NA18993.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-11-2301dupC | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 30951679 | |||||
| chr12:30951988
|
T | C | 184 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0086others(181): Show | 185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.-11-1993T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30951988 | ||||||
| chr12:30952037
|
A | G | 1 | a0002c0002t0066g0167 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-11-1944A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952037 | ||||||
| chr12:30952056
|
C | G | 1 | a0002c0002t0005g0322 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-11-1925C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952056 | ||||||
| chr12:30952060
|
G | A | 1 | a0001c0001t0009g0372 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-11-1921G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952060 | ||||||
| chr12:30952109
|
C | G | 11 | a0001c0001t0002g0220a0001c0001t0006g0222a0001c0001t0007g0200others(8): Show | 11 | HG00280.hp2 HG01069.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-1872C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952109 | ||||||
| chr12:30952149
|
T | C | 260 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0056others(257): Show | 261 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.-11-1832T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952149 | ||||||
| chr12:30952315
|
C | A | 6 | a0001c0001t0008g0063a0001c0001t0008g0089a0001c0001t0008g0093others(3): Show | 6 | NA18981.hp1 NA18990.hp1 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-1666C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952315 | ||||||
| chr12:30952327
|
C | T | 1 | a0006c0013t0011g0338 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-11-1654C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952327 | ||||||
| chr12:30952336
|
G | A | 51 | a0001c0001t0001g0113a0001c0001t0001g0230a0001c0001t0001g0257others(48): Show | 52 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-11-1645G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952336 | ||||||
| chr12:30952369
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-11-1612C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952369 | ||||||
| chr12:30952471
|
C | T | 1 | a0002c0002t0066g0167 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-11-1510C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952471 | ||||||
| chr12:30952506
|
C | T | 258 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0056others(255): Show | 260 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.-11-1475C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952506 | ||||||
| chr12:30952634
|
G | A | 2 | a0001c0001t0032g0268a0002c0002t0072g0153 | 2 | HG00408.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-11-1347G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952634 | ||||||
| chr12:30952641
|
C | A | 342 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0056others(339): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.-11-1340C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952641 | ||||||
| chr12:30952986
|
C | T | 1 | a0002c0004t0004g0283 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-11-995C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30952986 | ||||||
| chr12:30953100
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-11-881G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953100 | ||||||
| chr12:30953241
|
A | G | 1 | a0002c0002t0018g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-11-740A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953241 | ||||||
| chr12:30953362
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-11-619T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953362 | ||||||
| chr12:30953365
|
C | G | 2 | a0002c0002t0021g0034a0002c0002t0045g0037 | 2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11-616C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953365 | ||||||
| chr12:30953376
|
G | A | 1 | a0001c0001t0009g0204 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-11-605G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953376 | ||||||
| chr12:30953595
|
T | C | 3 | a0001c0001t0016g0178a0001c0001t0016g0331a0002c0002t0002g0315 | 3 | HG02965.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-11-386T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953595 | ||||||
| chr12:30953666
|
T | C | 1 | a0001c0001t0009g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-11-315T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953666 | ||||||
| chr12:30953707
|
C | T | 4 | a0001c0001t0056g0358a0002c0002t0013g0280a0002c0002t0015g0385others(1): Show | 4 | HG00738.hp1 HG02559.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-274C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953707 | ||||||
| chr12:30953716
|
T | C | 80 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(77): Show | 80 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-11-265T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953716 | ||||||
| chr12:30953852
|
A | G | 79 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(76): Show | 79 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.-11-129A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953852 | ||||||
| chr12:30953869
|
C | A | 79 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(76): Show | 79 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.-11-112C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953869 | ||||||
| chr12:30953913
|
T | G | 1 | a0002c0002t0006g0254 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-11-68T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953913 | ||||||
| chr12:30953922
|
G | A | 22 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(19): Show | 22 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.-11-59G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 1/7 | chr12 | 30953922 | ||||||
| chr12:30954197
|
A | G | 100 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(97): Show | 100 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.84+122A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30954197 | ||||||
| chr12:30954238
|
G | T | 1 | a0001c0001t0014g0369 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.84+163G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30954238 | ||||||
| chr12:30954389
|
T | G | 21 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.84+314T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30954389 | ||||||
| chr12:30954638
|
C | T | 10 | a0001c0001t0001g0203a0001c0001t0001g0351a0001c0001t0001g0353others(7): Show | 10 | HG01167.hp1 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.84+563C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30954638 | ||||||
| chr12:30954725
|
A | G | 3 | a0001c0001t0029g0192a0001c0001t0029g0193a0002c0002t0004g0295 | 3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.84+650A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30954725 | ||||||
| chr12:30954931
|
C | A | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.84+856C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30954931 | ||||||
| chr12:30955021
|
G | A | 316 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0056others(313): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.84+946G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30955021 | ||||||
| chr12:30955410
|
C | A | 5 | a0002c0005t0004g0004a0002c0005t0004g0361a0002c0005t0004g0362others(2): Show | 5 | HG02145.hp2 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+1335C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30955410 | ||||||
| chr12:30955434
|
G | A | 353 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0056others(350): Show | 356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.84+1359G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30955434 | ||||||
| chr12:30955503
|
G | A | 77 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(74): Show | 77 | HG00558.hp1 HG00609.hp1 HG01255.hp1 others(74): Show |
intron_variant | MODIFIER | c.84+1428G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30955503 | ||||||
| chr12:30955853
|
A | G | 2 | a0001c0007t0013g0243a0001c0007t0013g0249 | 2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.84+1778A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30955853 | ||||||
| chr12:30955937
|
C | T | 1 | a0001c0001t0025g0219 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.84+1862C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30955937 | ||||||
| chr12:30956145
|
A | C | 1 | a0002c0002t0001g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.84+2070A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956145 | ||||||
| chr12:30956263
|
G | A | 8 | a0001c0001t0002g0363a0001c0001t0029g0192a0001c0001t0029g0193others(5): Show | 8 | HG00738.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.84+2188G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956263 | ||||||
| chr12:30956438
|
T | G | 6 | a0001c0001t0004g0357a0001c0007t0013g0243a0001c0007t0013g0249others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+2363T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956438 | ||||||
| chr12:30956549
|
CT | C | 26 | a0001c0001t0002g0220a0001c0001t0006g0189a0001c0001t0006g0190others(23): Show | 26 | HG00280.hp2 HG01069.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.84+2475delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956549 | ||||||
| chr12:30956591
|
T | G | 2 | a0001c0001t0010g0029a0001c0001t0010g0324 | 2 | HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.84+2516T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956591 | ||||||
| chr12:30956666
|
A | G | 36 | a0001c0001t0001g0203a0001c0001t0001g0351a0001c0001t0001g0353others(33): Show | 36 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+2591A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956666 | ||||||
| chr12:30956716
|
TA | T | 175 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(172): Show | 176 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.84+2642delA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956716 | ||||||
| chr12:30956720
|
A | G | 175 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(172): Show | 176 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.84+2645A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956720 | ||||||
| chr12:30956764
|
G | A | 23 | a0001c0001t0002g0108a0001c0001t0039g0109a0003c0003t0001g0114others(20): Show | 23 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.84+2689G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956764 | ||||||
| chr12:30956827
|
C | T | 26 | a0001c0001t0002g0163a0001c0001t0002g0363a0001c0001t0002g0374others(23): Show | 26 | HG00438.hp1 HG00738.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.84+2752C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956827 | ||||||
| chr12:30956928
|
G | C | 23 | a0001c0001t0002g0108a0001c0001t0039g0109a0003c0003t0001g0114others(20): Show | 23 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.84+2853G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956928 | ||||||
| chr12:30956946
|
G | T | 1 | a0002c0002t0001g0314 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.84+2871G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956946 | ||||||
| chr12:30956947
|
T | A | 1 | a0002c0002t0001g0314 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.84+2872T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956947 | ||||||
| chr12:30956948
|
A | T | 1 | a0002c0002t0001g0314 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.84+2873A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956948 | ||||||
| chr12:30956962
|
C | A | 4 | a0001c0001t0001g0203a0001c0001t0016g0355a0001c0001t0018g0352others(1): Show | 4 | HG02717.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+2887C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30956962 | ||||||
| chr12:30957120
|
A | G | 62 | a0001c0001t0001g0146a0001c0001t0001g0288a0001c0001t0002g0210others(59): Show | 63 | HG00140.hp2 HG00438.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.84+3045A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957120 | ||||||
| chr12:30957122
|
A | G | 62 | a0001c0001t0001g0146a0001c0001t0001g0288a0001c0001t0002g0210others(59): Show | 63 | HG00140.hp2 HG00438.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.84+3047A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957122 | ||||||
| chr12:30957225
|
G | A | 1 | a0001c0001t0022g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.84+3150G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957225 | ||||||
| chr12:30957228
|
A | AC | 66 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0086others(63): Show | 66 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.84+3167dupC | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957228 | |||||
| chr12:30957228
|
A | ACC | 34 | a0001c0001t0001g0099a0001c0001t0001g0113a0001c0001t0001g0230others(31): Show | 35 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.84+3166_84+3167dup others(2): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957228 | |||||
| chr12:30957228
|
AC | A | 53 | a0001c0001t0001g0203a0001c0001t0001g0327a0001c0001t0001g0353others(50): Show | 54 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.84+3167delC | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957228 | |||||
| chr12:30957228
|
ACC | A | 58 | a0001c0001t0001g0101a0001c0001t0001g0197a0001c0001t0001g0240others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.84+3166_84+3167del others(2): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957228 | |||||
| chr12:30957228
|
ACCC | A | 54 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0146others(51): Show | 54 | HG00558.hp1 HG00738.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.84+3165_84+3167del others(3): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957228 | |||||
| chr12:30957228
|
ACCCC | A | 55 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0169others(52): Show | 56 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.84+3164_84+3167del others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957228 | |||||
| chr12:30957240
|
C | G | 1 | a0001c0001t0002g0350 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.84+3165C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957240 | ||||||
| chr12:30957241
|
C | A | 1 | a0001c0001t0063g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.84+3166C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957241 | ||||||
| chr12:30957335
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0021g0212 | 3 | HG02258.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84+3260G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957335 | ||||||
| chr12:30957369
|
A | T | 1 | a0001c0001t0006g0261 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.84+3294A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957369 | ||||||
| chr12:30957407
|
T | C | 1 | a0002c0002t0001g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.84+3332T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957407 | ||||||
| chr12:30957446
|
G | A | 14 | a0001c0001t0001g0146a0001c0001t0040g0255a0002c0002t0001g0142others(11): Show | 15 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+3371G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957446 | ||||||
| chr12:30957479
|
A | G | 1 | a0003c0003t0035g0321 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.84+3404A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957479 | ||||||
| chr12:30957514
|
T | C | 2 | a0001c0001t0001g0288a0001c0001t0002g0296 | 2 | HG03540.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.84+3439T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957514 | ||||||
| chr12:30957525
|
G | A | 1 | a0001c0001t0002g0287 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.84+3450G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957525 | ||||||
| chr12:30957541
|
T | C | 21 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.84+3466T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957541 | ||||||
| chr12:30957560
|
A | G | 29 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0163others(26): Show | 29 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.84+3485A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957560 | ||||||
| chr12:30957596
|
C | T | 3 | a0001c0001t0029g0192a0001c0001t0029g0193a0002c0002t0004g0295 | 3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.84+3521C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957596 | ||||||
| chr12:30957629
|
ATCCC | A | 11 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0004g0214others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.84+3576_84+3579del others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957629 | |||||
| chr12:30957629
|
ATCCCTCC others(5): Show |
A | 31 | a0001c0001t0002g0363a0001c0001t0006g0189a0001c0001t0006g0190others(28): Show | 31 | HG00738.hp1 HG01192.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.84+3568_84+3579del others(12): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957629 | |||||
| chr12:30957638
|
T | C | 1 | a0002c0002t0001g0314 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.84+3563T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957638 | ||||||
| chr12:30957703
|
CCCT | C | 53 | a0001c0001t0002g0363a0001c0001t0006g0189a0001c0001t0006g0190others(50): Show | 53 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.84+3632_84+3634del others(3): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957703 | |||||
| chr12:30957705
|
CTCCT | C | 11 | a0001c0001t0004g0006a0001c0001t0006g0284a0001c0001t0019g0388others(8): Show | 12 | HG01167.hp2 HG01169.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.84+3650_84+3653del others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957705 | |||||
| chr12:30957707
|
C | T | 3 | a0001c0001t0001g0288a0001c0001t0002g0296a0001c0001t0034g0228 | 3 | HG02622.hp2 HG03540.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.84+3632C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957707 | ||||||
| chr12:30957707
|
CCTT | C | 135 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(132): Show | 136 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.84+3634_84+3636del others(3): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957707 | |||||
| chr12:30957710
|
TCCTTCCT others(68): Show |
T | 3 | a0001c0001t0001g0288a0001c0001t0002g0296a0001c0001t0034g0228 | 3 | HG02622.hp2 HG03540.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.84+3636_84+3710del others(75): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957710 | ||||||
| chr12:30957712
|
C | T | 54 | a0001c0001t0002g0363a0001c0001t0006g0189a0001c0001t0006g0190others(51): Show | 54 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.84+3637C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957712 | ||||||
| chr12:30957713
|
TTCCTTCC others(81): Show |
T | 1 | a0002c0004t0001g0247 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.84+3726_84+3813del others(88): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957713 | |||||
| chr12:30957716
|
C | T | 135 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(132): Show | 136 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.84+3641C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957716 | ||||||
| chr12:30957721
|
TTCCTTCC others(61): Show |
T | 135 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(132): Show | 136 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.84+3654_84+3721del others(68): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957721 | |||||
| chr12:30957725
|
TTCCCTCC others(53): Show |
T | 3 | a0001c0001t0029g0192a0001c0001t0029g0193a0001c0001t0037g0014 | 3 | HG02895.hp2 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.84+3662_84+3721del others(60): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957725 | |||||
| chr12:30957729
|
CTCCTTCC others(17): Show |
C | 4 | a0001c0001t0002g0363a0002c0002t0013g0280a0002c0002t0015g0385others(1): Show | 4 | HG02145.hp1 HG02559.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+3662_84+3685del others(24): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957729 | |||||
| chr12:30957729
|
CTCCTTCC others(57): Show |
C | 27 | a0001c0001t0006g0189a0001c0001t0006g0190a0001c0001t0022g0051others(24): Show | 27 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.84+3666_84+3729del others(64): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957729 | |||||
| chr12:30957733
|
TTCCCTCC others(49): Show |
T | 3 | a0001c0001t0056g0358a0002c0002t0004g0295a0002c0004t0053g0019 | 3 | HG02622.hp1 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.84+3662_84+3717del others(56): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957733 | |||||
| chr12:30957741
|
C | T | 1 | a0001c0001t0005g0380 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.84+3666C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957741 | ||||||
| chr12:30957745
|
CTCCCTCC others(69): Show |
C | 1 | a0001c0001t0005g0380 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.84+3678_84+3753del others(76): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957745 | |||||
| chr12:30957759
|
C | T | 1 | a0001c0001t0020g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.84+3684C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957759 | ||||||
| chr12:30957761
|
TTCCTTCC others(69): Show |
T | 1 | a0001c0001t0014g0369 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.84+3702_84+3777del others(76): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957761 | |||||
| chr12:30957765
|
TTCCTTCC others(65): Show |
T | 5 | a0001c0001t0015g0366a0001c0001t0015g0367a0001c0001t0015g0368others(2): Show | 5 | HG01192.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+3702_84+3773del others(72): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957765 | |||||
| chr12:30957769
|
T | C | 4 | a0001c0001t0002g0363a0002c0002t0013g0280a0002c0002t0015g0385others(1): Show | 4 | HG02145.hp1 HG02559.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+3694T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957769 | ||||||
| chr12:30957769
|
TTCCTTCC others(61): Show |
T | 8 | a0001c0001t0014g0387a0001c0001t0016g0178a0001c0001t0016g0331others(5): Show | 8 | HG02809.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+3702_84+3769del others(68): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957769 | |||||
| chr12:30957773
|
TTCCCTCC others(49): Show |
T | 1 | a0002c0002t0002g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84+3710_84+3765del others(56): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957773 | |||||
| chr12:30957773
|
TTCCCTCC others(57): Show |
T | 2 | a0002c0002t0002g0184a0002c0004t0014g0195 | 2 | HG00738.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.84+3702_84+3765del others(64): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957773 | |||||
| chr12:30957777
|
CTCCCTCC others(77): Show |
C | 13 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0220others(10): Show | 13 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+3718_84+3801del others(84): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957777 | |||||
| chr12:30957789
|
C | T | 3 | a0001c0001t0001g0288a0001c0001t0002g0296a0001c0001t0034g0228 | 3 | HG02622.hp2 HG03540.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.84+3714C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957789 | ||||||
| chr12:30957793
|
T | C | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.84+3718T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957793 | ||||||
| chr12:30957793
|
TTCCTTCC others(77): Show |
T | 13 | a0001c0001t0002g0163a0001c0001t0002g0374a0001c0001t0002g0375others(10): Show | 13 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+3726_84+3809del others(84): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957793 | |||||
| chr12:30957801
|
C | T | 34 | a0001c0001t0002g0363a0001c0001t0006g0189a0001c0001t0006g0190others(31): Show | 34 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.84+3726C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957801 | ||||||
| chr12:30957805
|
T | C | 3 | a0001c0001t0029g0192a0001c0001t0029g0193a0001c0001t0037g0014 | 3 | HG02895.hp2 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.84+3730T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957805 | ||||||
| chr12:30957809
|
T | C | 30 | a0001c0001t0006g0189a0001c0001t0006g0190a0001c0001t0022g0051others(27): Show | 30 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.84+3734T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957809 | ||||||
| chr12:30957809
|
TTCCTTCC others(21): Show |
T | 1 | a0002c0002t0018g0038 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.84+3742_84+3769del others(28): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957809 | |||||
| chr12:30957813
|
T | C | 6 | a0001c0001t0029g0192a0001c0001t0029g0193a0001c0001t0037g0014others(3): Show | 6 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+3738T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957813 | ||||||
| chr12:30957813
|
TTCCCTCC others(13): Show |
T | 1 | a0002c0002t0013g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.84+3750_84+3769del others(20): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957813 | |||||
| chr12:30957813
|
TTCCCTCC others(17): Show |
T | 2 | a0001c0001t0002g0363a0002c0002t0015g0385 | 2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.84+3742_84+3765del others(24): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957813 | |||||
| chr12:30957821
|
T | C | 33 | a0001c0001t0006g0189a0001c0001t0006g0190a0001c0001t0022g0051others(30): Show | 33 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.84+3746T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957821 | ||||||
| chr12:30957825
|
C | T | 2 | a0001c0001t0056g0358a0002c0004t0053g0019 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.84+3750C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957825 | ||||||
| chr12:30957829
|
C | T | 6 | a0001c0001t0029g0192a0001c0001t0029g0193a0001c0001t0037g0014others(3): Show | 6 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+3754C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957829 | ||||||
| chr12:30957833
|
C | T | 34 | a0001c0001t0006g0189a0001c0001t0006g0190a0001c0001t0022g0051others(31): Show | 34 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.84+3758C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957833 | ||||||
| chr12:30957837
|
C | T | 37 | a0001c0001t0001g0262a0001c0001t0005g0380a0001c0001t0006g0189others(34): Show | 37 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.84+3762C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957837 | ||||||
| chr12:30957837
|
CTCCT | C | 59 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(56): Show | 59 | HG00558.hp1 HG00609.hp1 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.84+3786_84+3789del others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957837 | |||||
| chr12:30957857
|
T | C | 1 | a0001c0001t0037g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.84+3782T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957857 | ||||||
| chr12:30957857
|
TTCCTTCC others(1): Show |
T | 8 | a0001c0001t0003g0094a0001c0001t0003g0098a0001c0001t0003g0110others(5): Show | 8 | HG04184.hp1 NA18956.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+3786_84+3793del others(8): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957857 | |||||
| chr12:30957861
|
T | C | 75 | a0001c0001t0001g0197a0001c0001t0001g0262a0001c0001t0001g0356others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.84+3786T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957861 | ||||||
| chr12:30957861
|
T | TTCCC | 180 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0086others(177): Show | 183 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.84+3802_84+3805dup others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957861 | |||||
| chr12:30957861
|
T | TTCCTTCC others(1): Show |
3 | a0002c0002t0021g0034a0002c0002t0045g0037a0002c0004t0017g0152 | 3 | HG01981.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.84+3789_84+3790ins others(8): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30957861 | |||||
| chr12:30957877
|
C | T | 16 | a0001c0001t0001g0197a0001c0001t0001g0356a0001c0001t0004g0186others(13): Show | 16 | HG01167.hp1 HG01891.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.84+3802C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957877 | ||||||
| chr12:30957881
|
T | C | 8 | a0001c0001t0003g0094a0001c0001t0003g0098a0001c0001t0003g0110others(5): Show | 8 | HG04184.hp1 NA18956.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+3806T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30957881 | ||||||
| chr12:30958007
|
C | T | 15 | a0001c0001t0001g0197a0001c0001t0001g0356a0001c0001t0004g0186others(12): Show | 15 | HG01167.hp1 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.84+3932C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958007 | ||||||
| chr12:30958028
|
G | C | 1 | a0002c0002t0030g0308 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.84+3953G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958028 | ||||||
| chr12:30958207
|
G | A | 1 | a0001c0001t0037g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.84+4132G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958207 | ||||||
| chr12:30958366
|
G | A | 20 | a0001c0001t0014g0369a0001c0001t0014g0387a0001c0001t0015g0366others(17): Show | 20 | HG00738.hp1 HG01192.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.84+4291G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958366 | ||||||
| chr12:30958410
|
C | A | 4 | a0001c0001t0001g0356a0001c0001t0034g0228a0002c0002t0014g0124others(1): Show | 4 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+4335C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958410 | ||||||
| chr12:30958446
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.84+4371C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958446 | ||||||
| chr12:30958454
|
T | C | 82 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0163others(79): Show | 82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.84+4379T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958454 | ||||||
| chr12:30958492
|
C | G | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.84+4417C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958492 | ||||||
| chr12:30958548
|
G | A | 1 | a0002c0002t0001g0069 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.84+4473G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958548 | ||||||
| chr12:30958658
|
C | G | 2 | a0002c0002t0018g0038a0002c0004t0053g0019 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.84+4583C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958658 | ||||||
| chr12:30958683
|
C | T | 82 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0163others(79): Show | 82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.84+4608C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958683 | ||||||
| chr12:30958695
|
A | T | 1 | a0001c0001t0037g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.84+4620A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958695 | ||||||
| chr12:30958702
|
C | T | 14 | a0001c0001t0001g0080a0001c0001t0001g0112a0001c0001t0001g0146others(11): Show | 14 | HG00609.hp1 HG02015.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.84+4627C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958702 | ||||||
| chr12:30958856
|
T | C | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.84+4781T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958856 | ||||||
| chr12:30958915
|
C | A | 5 | a0001c0001t0001g0203a0001c0001t0004g0357a0001c0001t0016g0355others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+4840C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30958915 | ||||||
| chr12:30959076
|
G | A | 2 | a0001c0001t0031g0102a0001c0001t0031g0207 | 2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.85-4750G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959076 | ||||||
| chr12:30959161
|
G | A | 1 | a0002c0002t0001g0310 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.85-4665G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959161 | ||||||
| chr12:30959191
|
C | T | 1 | a0002c0002t0001g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.85-4635C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959191 | ||||||
| chr12:30959192
|
G | A | 1 | a0001c0001t0063g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.85-4634G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959192 | ||||||
| chr12:30959237
|
G | C | 1 | a0001c0001t0001g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.85-4589G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959237 | ||||||
| chr12:30959350
|
T | C | 1 | a0002c0002t0007g0095 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.85-4476T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959350 | ||||||
| chr12:30959362
|
G | A | 4 | a0001c0001t0024g0180a0001c0001t0028g0181a0001c0001t0028g0316others(1): Show | 4 | HG02257.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-4464G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959362 | ||||||
| chr12:30959418
|
C | G | 84 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0163others(81): Show | 84 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.85-4408C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959418 | ||||||
| chr12:30959482
|
T | G | 16 | a0001c0001t0014g0369a0001c0001t0014g0387a0001c0001t0015g0366others(13): Show | 16 | HG01192.hp1 HG02109.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.85-4344T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959482 | ||||||
| chr12:30959538
|
T | C | 5 | a0001c0001t0001g0203a0001c0001t0004g0357a0001c0001t0016g0355others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-4288T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959538 | ||||||
| chr12:30959614
|
G | GA | 63 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0163others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.85-4204dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30959614 | |||||
| chr12:30959614
|
G | GAA | 21 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-4205_85-4204dup others(2): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30959614 | |||||
| chr12:30959648
|
C | T | 21 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-4178C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959648 | ||||||
| chr12:30959719
|
G | T | 42 | a0001c0001t0001g0203a0001c0001t0001g0288a0001c0001t0002g0210others(39): Show | 42 | HG00738.hp2 HG01074.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.85-4107G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959719 | ||||||
| chr12:30959735
|
A | G | 96 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0163others(93): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.85-4091A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959735 | ||||||
| chr12:30959779
|
C | CA | 74 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0080others(71): Show | 74 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.85-4027dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30959779 | |||||
| chr12:30959779
|
CA | C | 9 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0004g0214others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-4027delA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30959779 | |||||
| chr12:30959795
|
A | AAC | 30 | a0001c0001t0002g0163a0001c0001t0002g0375a0001c0001t0002g0376others(27): Show | 30 | HG00438.hp1 HG00673.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.85-4030_85-4029ins others(2): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30959795 | |||||
| chr12:30959795
|
A | AC | 51 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0220others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.85-4031_85-4030ins others(1): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959795 | ||||||
| chr12:30959802
|
G | A | 1 | a0002c0002t0018g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.85-4024G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959802 | ||||||
| chr12:30959874
|
G | A | 11 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0004g0214others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.85-3952G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959874 | ||||||
| chr12:30959884
|
A | G | 1 | a0001c0001t0002g0287 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.85-3942A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959884 | ||||||
| chr12:30959999
|
C | T | 1 | a0002c0002t0045g0037 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.85-3827C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30959999 | ||||||
| chr12:30960030
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.85-3796C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960030 | ||||||
| chr12:30960063
|
G | C | 1 | a0002c0002t0018g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.85-3763G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960063 | ||||||
| chr12:30960082
|
A | G | 84 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0163others(81): Show | 84 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.85-3744A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960082 | ||||||
| chr12:30960121
|
T | TGTGG | 5 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0034g0008others(2): Show | 5 | HG01884.hp1 HG02257.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-3685_85-3682dup others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30960121 | |||||
| chr12:30960129
|
G | A | 4 | a0001c0001t0056g0358a0002c0002t0013g0280a0002c0002t0015g0385others(1): Show | 4 | HG00738.hp1 HG02559.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-3697G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960129 | ||||||
| chr12:30960178
|
A | G | 1 | a0001c0001t0056g0358 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.85-3648A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960178 | ||||||
| chr12:30960199
|
T | A | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-3627T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960199 | ||||||
| chr12:30960316
|
A | G | 20 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(17): Show | 20 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.85-3510A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960316 | ||||||
| chr12:30960464
|
T | C | 1 | a0001c0001t0003g0111 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.85-3362T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960464 | ||||||
| chr12:30960466
|
T | C | 141 | a0001c0001t0001g0203a0001c0001t0001g0244a0001c0001t0001g0245others(138): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.85-3360T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960466 | ||||||
| chr12:30960529
|
G | A | 68 | a0001c0001t0001g0099a0001c0001t0001g0257a0001c0001t0001g0342others(65): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.85-3297G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960529 | ||||||
| chr12:30960542
|
T | TTTCTCTC others(32): Show |
1 | a0001c0001t0023g0336 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.85-3283_85-3245dup others(39): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30960542 | |||||
| chr12:30960564
|
G | A | 2 | a0001c0001t0008g0047a0001c0001t0008g0084 | 2 | NA18946.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.85-3262G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960564 | ||||||
| chr12:30960615
|
C | T | 21 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-3211C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960615 | ||||||
| chr12:30960655
|
C | T | 1 | a0002c0002t0007g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.85-3171C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960655 | ||||||
| chr12:30960676
|
A | G | 183 | a0001c0001t0001g0099a0001c0001t0001g0203a0001c0001t0001g0244others(180): Show | 186 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.85-3150A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960676 | ||||||
| chr12:30960679
|
C | T | 3 | a0003c0003t0006g0232a0003c0003t0006g0270a0003c0003t0062g0265 | 3 | NA18956.hp2 NA18979.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.85-3147C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960679 | ||||||
| chr12:30960685
|
G | A | 1 | a0002c0002t0001g0157 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.85-3141G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960685 | ||||||
| chr12:30960808
|
G | C | 1 | a0002c0002t0047g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85-3018G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960808 | ||||||
| chr12:30960912
|
A | G | 21 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-2914A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960912 | ||||||
| chr12:30960965
|
G | A | 3 | a0001c0001t0034g0228a0002c0002t0014g0124a0011c0010t0022g0185 | 3 | HG01167.hp1 HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.85-2861G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30960965 | ||||||
| chr12:30961017
|
C | T | 1 | a0001c0001t0037g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.85-2809C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961017 | ||||||
| chr12:30961029
|
G | GA | 134 | a0001c0001t0001g0099a0001c0001t0001g0165a0001c0001t0001g0244others(131): Show | 136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.85-2783dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30961029 | |||||
| chr12:30961029
|
GA | G | 6 | a0001c0001t0008g0306a0001c0001t0016g0187a0001c0001t0034g0228others(3): Show | 6 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-2783delA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30961029 | |||||
| chr12:30961029
|
GAA | G | 20 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(17): Show | 20 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.85-2784_85-2783del others(2): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30961029 | |||||
| chr12:30961096
|
C | A | 1 | a0002c0004t0005g0272 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.85-2730C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961096 | ||||||
| chr12:30961174
|
G | A | 127 | a0001c0001t0001g0099a0001c0001t0001g0244a0001c0001t0001g0245others(124): Show | 129 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.85-2652G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961174 | ||||||
| chr12:30961213
|
A | C | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2613A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961213 | ||||||
| chr12:30961214
|
G | T | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2612G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961214 | ||||||
| chr12:30961216
|
C | A | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2610C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961216 | ||||||
| chr12:30961217
|
A | C | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2609A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961217 | ||||||
| chr12:30961218
|
G | C | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2608G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961218 | ||||||
| chr12:30961220
|
T | C | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2606T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961220 | ||||||
| chr12:30961222
|
C | G | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2604C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961222 | ||||||
| chr12:30961224
|
A | T | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2602A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961224 | ||||||
| chr12:30961226
|
G | A | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2600G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961226 | ||||||
| chr12:30961228
|
G | T | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2598G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961228 | ||||||
| chr12:30961229
|
G | A | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2597G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961229 | ||||||
| chr12:30961230
|
C | T | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2596C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961230 | ||||||
| chr12:30961232
|
T | C | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2594T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961232 | ||||||
| chr12:30961233
|
G | A | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2593G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961233 | ||||||
| chr12:30961235
|
G | T | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2591G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961235 | ||||||
| chr12:30961241
|
G | A | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2585G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961241 | ||||||
| chr12:30961244
|
A | T | 1 | a0001c0001t0002g0374 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85-2582A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961244 | ||||||
| chr12:30961298
|
T | C | 21 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-2528T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961298 | ||||||
| chr12:30961347
|
T | C | 129 | a0001c0001t0001g0099a0001c0001t0001g0244a0001c0001t0001g0245others(126): Show | 131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.85-2479T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961347 | ||||||
| chr12:30961440
|
A | T | 46 | a0001c0001t0001g0042a0001c0001t0001g0101a0001c0001t0001g0240others(43): Show | 46 | HG00558.hp1 HG01928.hp2 HG01943.hp1 others(43): Show |
intron_variant | MODIFIER | c.85-2386A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961440 | ||||||
| chr12:30961620
|
G | T | 3 | a0001c0001t0034g0228a0002c0002t0014g0124a0011c0010t0022g0185 | 3 | HG01167.hp1 HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.85-2206G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961620 | ||||||
| chr12:30961636
|
G | A | 55 | a0001c0001t0001g0203a0001c0001t0001g0288a0001c0001t0002g0210others(52): Show | 56 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.85-2190G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961636 | ||||||
| chr12:30961727
|
A | T | 21 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-2099A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961727 | ||||||
| chr12:30961824
|
C | G | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.85-2002C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961824 | ||||||
| chr12:30961849
|
G | A | 6 | a0001c0001t0001g0056a0001c0001t0003g0040a0001c0001t0003g0057others(3): Show | 6 | HG00408.hp1 HG00609.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-1977G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961849 | ||||||
| chr12:30961961
|
A | G | 67 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(64): Show | 67 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.85-1865A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30961961 | ||||||
| chr12:30962036
|
C | T | 21 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-1790C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962036 | ||||||
| chr12:30962043
|
T | C | 2 | a0001c0001t0029g0192a0001c0001t0029g0193 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.85-1783T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962043 | ||||||
| chr12:30962076
|
A | G | 11 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0004g0214others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.85-1750A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962076 | ||||||
| chr12:30962170
|
G | A | 14 | a0001c0001t0002g0163a0001c0001t0002g0374a0001c0001t0002g0375others(11): Show | 14 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.85-1656G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962170 | ||||||
| chr12:30962220
|
G | A | 1 | a0004c0006t0001g0134 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.85-1606G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962220 | ||||||
| chr12:30962347
|
A | C | 1 | a0001c0001t0001g0043 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.85-1479A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962347 | ||||||
| chr12:30962411
|
A | C | 283 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0099others(280): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.85-1415A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962411 | ||||||
| chr12:30962494
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.85-1332A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962494 | ||||||
| chr12:30962558
|
G | A | 11 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0004g0214others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.85-1268G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962558 | ||||||
| chr12:30962611
|
A | G | 109 | a0001c0001t0001g0099a0001c0001t0001g0244a0001c0001t0001g0245others(106): Show | 111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.85-1215A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962611 | ||||||
| chr12:30962641
|
C | T | 16 | a0001c0001t0002g0163a0001c0001t0002g0374a0001c0001t0002g0375others(13): Show | 16 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.85-1185C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962641 | ||||||
| chr12:30962712
|
A | G | 1 | a0001c0001t0044g0317 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.85-1114A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962712 | ||||||
| chr12:30962727
|
A | G | 283 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0099others(280): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.85-1099A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962727 | ||||||
| chr12:30962783
|
C | T | 85 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0288others(82): Show | 86 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.85-1043C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962783 | ||||||
| chr12:30962798
|
A | C | 351 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0056others(348): Show | 354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.85-1028A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962798 | ||||||
| chr12:30962829
|
A | G | 110 | a0001c0001t0001g0099a0001c0001t0001g0244a0001c0001t0001g0245others(107): Show | 112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.85-997A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962829 | ||||||
| chr12:30962868
|
C | G | 21 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-958C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962868 | ||||||
| chr12:30962944
|
A | T | 5 | a0001c0001t0002g0210a0001c0001t0002g0345a0001c0001t0010g0209others(2): Show | 5 | HG01243.hp1 HG01258.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-882A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962944 | ||||||
| chr12:30962972
|
A | G | 1 | a0003c0003t0003g0078 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.85-854A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962972 | ||||||
| chr12:30962996
|
G | C | 110 | a0001c0001t0001g0099a0001c0001t0001g0244a0001c0001t0001g0245others(107): Show | 112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.85-830G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30962996 | ||||||
| chr12:30963077
|
C | G | 14 | a0001c0001t0020g0024a0002c0002t0001g0142a0002c0002t0005g0130others(11): Show | 15 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.85-749C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963077 | ||||||
| chr12:30963102
|
GA | G | 66 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(63): Show | 66 | HG00558.hp1 HG00609.hp1 HG01928.hp2 others(63): Show |
intron_variant | MODIFIER | c.85-722delA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 30963102 | |||||
| chr12:30963110
|
C | A | 1 | a0001c0001t0033g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.85-716C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963110 | ||||||
| chr12:30963270
|
G | C | 66 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(63): Show | 66 | HG00558.hp1 HG00609.hp1 HG01928.hp2 others(63): Show |
intron_variant | MODIFIER | c.85-556G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963270 | ||||||
| chr12:30963371
|
A | T | 66 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(63): Show | 66 | HG00558.hp1 HG00609.hp1 HG01928.hp2 others(63): Show |
intron_variant | MODIFIER | c.85-455A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963371 | ||||||
| chr12:30963552
|
C | T | 8 | a0001c0001t0001g0288a0001c0001t0002g0296a0001c0001t0005g0301others(5): Show | 8 | HG00738.hp2 HG01074.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-274C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963552 | ||||||
| chr12:30963622
|
G | T | 3 | a0001c0001t0034g0228a0002c0002t0014g0124a0011c0010t0022g0185 | 3 | HG01167.hp1 HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.85-204G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963622 | ||||||
| chr12:30963663
|
G | A | 1 | a0001c0001t0037g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.85-163G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963663 | ||||||
| chr12:30963743
|
G | T | 2 | a0001c0001t0031g0102a0001c0001t0031g0207 | 2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.85-83G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963743 | ||||||
| chr12:30963795
|
C | A | 5 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0034g0008others(2): Show | 5 | HG01884.hp1 HG02257.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-31C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963795 | ||||||
| chr12:30963804
|
C | G | 1 | a0001c0001t0016g0365 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.85-22C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963804 | ||||||
| chr12:30963810
|
C | T | 21 | a0001c0001t0001g0043a0001c0001t0001g0154a0001c0001t0001g0169others(18): Show | 21 | HG00558.hp2 HG01099.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-16C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 2/7 | chr12 | 30963810 | ||||||
| chr12:30964106
|
AGTGGGAG others(11): Show |
A | 60 | a0001c0001t0001g0203a0001c0001t0001g0288a0001c0001t0002g0210others(57): Show | 61 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.276+97_276+114delG others(17): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30964106 | |||||
| chr12:30964374
|
C | T | 67 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0101others(64): Show | 67 | HG00558.hp1 HG00609.hp1 HG01928.hp2 others(64): Show |
intron_variant | MODIFIER | c.276+357C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964374 | ||||||
| chr12:30964380
|
CT | C | 14 | a0001c0001t0014g0369a0001c0001t0015g0366a0001c0001t0015g0367others(11): Show | 14 | HG01192.hp1 HG02109.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.276+365delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30964380 | |||||
| chr12:30964424
|
C | G | 1 | a0002c0002t0001g0073 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.276+407C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964424 | ||||||
| chr12:30964426
|
C | CCCTCTTC others(5): Show |
55 | a0001c0001t0001g0288a0001c0001t0002g0210a0001c0001t0002g0287others(52): Show | 56 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.276+420_276+431dup others(12): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30964426 | |||||
| chr12:30964604
|
A | C | 2 | a0001c0001t0034g0228a0011c0010t0022g0185 | 2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.276+587A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964604 | ||||||
| chr12:30964611
|
A | C | 3 | a0001c0001t0022g0051a0002c0002t0004g0318a0002c0002t0046g0188 | 3 | HG02809.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.276+594A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964611 | ||||||
| chr12:30964661
|
G | C | 1 | a0001c0001t0011g0065 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.276+644G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964661 | ||||||
| chr12:30964785
|
A | G | 6 | a0001c0001t0005g0048a0001c0001t0011g0085a0001c0001t0011g0097others(3): Show | 6 | HG01952.hp2 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+768A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964785 | ||||||
| chr12:30964865
|
T | C | 2 | a0001c0001t0002g0374a0001c0001t0002g0375 | 2 | HG00438.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.276+848T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964865 | ||||||
| chr12:30964913
|
G | A | 1 | a0001c0001t0002g0269 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.276+896G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964913 | ||||||
| chr12:30964924
|
C | A | 1 | a0001c0001t0002g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.276+907C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30964924 | ||||||
| chr12:30965126
|
G | A | 1 | a0001c0001t0056g0358 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.276+1109G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965126 | ||||||
| chr12:30965132
|
C | T | 2 | a0001c0001t0001g0288a0001c0001t0002g0296 | 2 | HG03540.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.276+1115C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965132 | ||||||
| chr12:30965160
|
C | A | 6 | a0001c0001t0010g0127a0001c0001t0010g0273a0001c0001t0027g0022others(3): Show | 6 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+1143C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965160 | ||||||
| chr12:30965172
|
C | T | 2 | a0001c0001t0007g0092a0002c0002t0007g0100 | 2 | NA19012.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.276+1155C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965172 | ||||||
| chr12:30965253
|
G | A | 1 | a0002c0002t0004g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.276+1236G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965253 | ||||||
| chr12:30965262
|
C | A | 10 | a0001c0001t0001g0197a0001c0001t0004g0214a0001c0001t0016g0365others(7): Show | 10 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.276+1245C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965262 | ||||||
| chr12:30965360
|
C | T | 28 | a0001c0001t0001g0197a0001c0001t0002g0163a0001c0001t0002g0374others(25): Show | 28 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.276+1343C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965360 | ||||||
| chr12:30965395
|
A | T | 5 | a0001c0001t0001g0327a0001c0001t0003g0196a0001c0001t0008g0306others(2): Show | 5 | NA18946.hp1 NA18947.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+1378A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965395 | ||||||
| chr12:30965440
|
A | G | 257 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(254): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.276+1423A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965440 | ||||||
| chr12:30965459
|
C | G | 5 | a0001c0001t0012g0032a0002c0002t0001g0035a0002c0002t0001g0036others(2): Show | 5 | HG02080.hp1 HG02523.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+1442C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965459 | ||||||
| chr12:30965459
|
C | T | 2 | a0001c0001t0005g0301a0001c0001t0017g0302 | 2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.276+1442C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965459 | ||||||
| chr12:30965461
|
A | C | 1 | a0001c0001t0003g0117 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.276+1444A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965461 | ||||||
| chr12:30965463
|
C | CGCCTTCC others(11): Show |
11 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0004g0214others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.276+1450_276+1467d others(20): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30965463 | |||||
| chr12:30965536
|
T | A | 1 | a0002c0002t0003g0091 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.276+1519T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965536 | ||||||
| chr12:30965570
|
A | G | 73 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(70): Show | 73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.276+1553A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965570 | ||||||
| chr12:30965591
|
A | G | 6 | a0001c0001t0001g0203a0001c0001t0004g0357a0001c0001t0016g0355others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+1574A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965591 | ||||||
| chr12:30965662
|
C | T | 1 | a0001c0001t0011g0097 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.276+1645C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965662 | ||||||
| chr12:30965675
|
C | CACA | 3 | a0001c0001t0003g0383a0001c0001t0006g0030a0002c0004t0001g0234 | 3 | HG00621.hp1 HG02074.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.276+1660_276+1661i others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30965675 | |||||
| chr12:30965675
|
C | T | 61 | a0001c0001t0001g0203a0001c0001t0001g0288a0001c0001t0002g0210others(58): Show | 62 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.276+1658C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965675 | ||||||
| chr12:30965679
|
T | C | 101 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(98): Show | 101 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.276+1662T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965679 | ||||||
| chr12:30965717
|
G | A | 8 | a0001c0001t0001g0240a0001c0001t0008g0063a0001c0001t0008g0067others(5): Show | 8 | NA18942.hp2 NA18954.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.276+1700G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965717 | ||||||
| chr12:30965940
|
G | A | 2 | a0001c0001t0008g0047a0001c0001t0008g0084 | 2 | NA18946.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.276+1923G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30965940 | ||||||
| chr12:30966002
|
TTA | T | 57 | a0001c0001t0001g0099a0001c0001t0001g0257a0001c0001t0001g0342others(54): Show | 58 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.276+1987_276+1988d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30966002 | |||||
| chr12:30966021
|
A | AT | 130 | a0001c0001t0001g0099a0001c0001t0001g0244a0001c0001t0001g0245others(127): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.276+2018dupT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30966021 | |||||
| chr12:30966021
|
AT | A | 7 | a0001c0001t0006g0190a0001c0001t0024g0180a0001c0001t0028g0181others(4): Show | 7 | HG01891.hp1 HG02027.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.276+2018delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30966021 | |||||
| chr12:30966021
|
ATT | A | 72 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(69): Show | 72 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.276+2017_276+2018d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30966021 | |||||
| chr12:30966081
|
G | T | 14 | a0001c0001t0002g0163a0001c0001t0002g0374a0001c0001t0002g0375others(11): Show | 14 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.276+2064G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966081 | ||||||
| chr12:30966104
|
C | T | 1 | a0001c0001t0022g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.276+2087C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966104 | ||||||
| chr12:30966106
|
A | G | 5 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0034g0008others(2): Show | 5 | HG01884.hp1 HG02257.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+2089A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966106 | ||||||
| chr12:30966117
|
C | A | 1 | a0001c0001t0009g0229 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.276+2100C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966117 | ||||||
| chr12:30966137
|
T | C | 180 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(177): Show | 181 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.276+2120T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966137 | ||||||
| chr12:30966189
|
G | C | 28 | a0001c0001t0001g0197a0001c0001t0002g0163a0001c0001t0002g0374others(25): Show | 28 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.276+2172G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966189 | ||||||
| chr12:30966261
|
C | T | 1 | a0005c0017t0011g0171 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.276+2244C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966261 | ||||||
| chr12:30966262
|
G | A | 1 | a0002c0004t0053g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.276+2245G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966262 | ||||||
| chr12:30966371
|
G | A | 11 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0004g0214others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.276+2354G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966371 | ||||||
| chr12:30966533
|
A | G | 73 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(70): Show | 73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.276+2516A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966533 | ||||||
| chr12:30966589
|
G | A | 29 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0220others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.276+2572G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966589 | ||||||
| chr12:30966613
|
T | TAAG | 5 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0034g0008others(2): Show | 5 | HG01884.hp1 HG02257.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+2598_276+2600d others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30966613 | |||||
| chr12:30966661
|
G | A | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.276+2644G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966661 | ||||||
| chr12:30966677
|
G | C | 1 | a0001c0001t0005g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.276+2660G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966677 | ||||||
| chr12:30966688
|
G | A | 1 | a0002c0002t0021g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.276+2671G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966688 | ||||||
| chr12:30966861
|
G | A | 2 | a0001c0001t0051g0177a0002c0002t0004g0295 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.276+2844G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966861 | ||||||
| chr12:30966867
|
C | T | 6 | a0001c0001t0001g0203a0001c0001t0004g0357a0001c0001t0016g0355others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+2850C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966867 | ||||||
| chr12:30966937
|
C | T | 1 | a0002c0002t0001g0199 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.276+2920C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30966937 | ||||||
| chr12:30967001
|
G | A | 14 | a0001c0001t0001g0327a0001c0001t0003g0196a0001c0001t0008g0058others(11): Show | 14 | HG02056.hp1 HG02165.hp1 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.276+2984G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967001 | ||||||
| chr12:30967055
|
G | C | 1 | a0001c0001t0019g0388 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.276+3038G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967055 | ||||||
| chr12:30967208
|
G | A | 1 | a0001c0001t0006g0328 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.276+3191G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967208 | ||||||
| chr12:30967227
|
G | T | 11 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0004g0214others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.276+3210G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967227 | ||||||
| chr12:30967412
|
C | T | 1 | a0001c0001t0023g0170 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.276+3395C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967412 | ||||||
| chr12:30967661
|
C | T | 100 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(97): Show | 100 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.276+3644C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967661 | ||||||
| chr12:30967674
|
GTGCACAC others(13): Show |
G | 105 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(102): Show | 105 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.276+3678_276+3697d others(22): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967674 | |||||
| chr12:30967678
|
ACACACAT others(31): Show |
A | 104 | a0001c0001t0001g0099a0001c0001t0001g0244a0001c0001t0001g0245others(101): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.276+3672_276+3709d others(40): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967678 | |||||
| chr12:30967695
|
T | C | 1 | a0001c0001t0003g0117 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.276+3678T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967695 | ||||||
| chr12:30967695
|
TGCACACA others(13): Show |
T | 5 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0034g0008others(2): Show | 5 | HG01884.hp1 HG02257.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+3686_276+3705d others(22): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967695 | |||||
| chr12:30967699
|
CACACATG others(14): Show |
C | 1 | a0001c0001t0003g0117 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.276+3683_276+3703d others(23): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967699 | ||||||
| chr12:30967722
|
A | C | 1 | a0001c0001t0003g0117 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.276+3705A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967722 | ||||||
| chr12:30967773
|
C | T | 1 | a0001c0001t0003g0116 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.276+3756C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967773 | ||||||
| chr12:30967774
|
G | A | 1 | a0002c0002t0026g0299 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.276+3757G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967774 | ||||||
| chr12:30967795
|
T | TGGCCTAG others(302): Show |
1 | a0002c0002t0007g0141 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.276+3799_276+3800i others(311): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(305): Show |
1 | a0001c0001t0016g0187 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.276+3799_276+3800i others(314): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(307): Show |
1 | a0002c0002t0075g0149 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(316): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(310): Show |
1 | a0001c0001t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.276+3799_276+3800i others(319): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(311): Show |
4 | a0001c0001t0004g0011a0001c0001t0034g0008a0001c0001t0049g0010others(1): Show | 4 | HG01884.hp1 HG02257.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.276+3799_276+3800i others(320): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(311): Show |
18 | a0001c0001t0001g0288a0001c0001t0002g0296a0001c0001t0005g0301others(15): Show | 18 | HG01074.hp1 HG01123.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.276+3799_276+3800i others(320): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(312): Show |
1 | a0002c0002t0004g0300 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.276+3799_276+3800i others(321): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(315): Show |
1 | a0002c0004t0017g0152 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(324): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(317): Show |
4 | a0001c0001t0001g0203a0001c0001t0016g0355a0002c0002t0018g0354others(1): Show | 4 | HG02717.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+3799_276+3800i others(326): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(318): Show |
2 | a0001c0001t0004g0357a0001c0001t0018g0352 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.276+3799_276+3800i others(327): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(323): Show |
1 | a0001c0001t0002g0345 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(332): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(324): Show |
2 | a0001c0001t0006g0190a0002c0002t0007g0140 | 2 | HG02897.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.276+3799_276+3800i others(333): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(325): Show |
1 | a0001c0001t0006g0189 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(334): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(326): Show |
1 | a0001c0001t0059g0332 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(335): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(334): Show |
1 | a0001c0001t0002g0298 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.276+3799_276+3800i others(343): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(335): Show |
1 | a0002c0002t0007g0144 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.276+3799_276+3800i others(344): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(335): Show |
5 | a0001c0001t0002g0287a0001c0001t0002g0330a0001c0001t0010g0209others(2): Show | 5 | HG01943.hp2 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+3799_276+3800i others(344): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(336): Show |
3 | a0002c0002t0006g0132a0002c0002t0007g0128a0002c0002t0026g0025 | 3 | HG02080.hp2 HG02895.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.276+3799_276+3800i others(345): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(336): Show |
2 | a0001c0001t0002g0210a0002c0002t0041g0012 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.276+3799_276+3800i others(345): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(337): Show |
1 | a0001c0001t0020g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(346): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(340): Show |
1 | a0001c0001t0023g0336 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(349): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(341): Show |
1 | a0002c0002t0005g0143 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(350): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(341): Show |
1 | a0001c0001t0023g0337 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.276+3799_276+3800i others(350): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(342): Show |
2 | a0002c0002t0005g0131a0002c0002t0007g0005 | 3 | NA18951.hp2 NA18959.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.276+3799_276+3800i others(351): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967795
|
T | TGGCCTAG others(343): Show |
3 | a0002c0002t0001g0142a0002c0002t0005g0130a0002c0002t0007g0150 | 3 | HG00438.hp2 NA18994.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.276+3799_276+3800i others(352): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30967795 | |||||
| chr12:30967970
|
A | G | 72 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(69): Show | 72 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.276+3953A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967970 | ||||||
| chr12:30967986
|
C | T | 4 | a0001c0001t0024g0180a0001c0001t0028g0181a0001c0001t0028g0316others(1): Show | 4 | HG02257.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.276+3969C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30967986 | ||||||
| chr12:30968126
|
G | A | 1 | a0002c0002t0018g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.276+4109G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968126 | ||||||
| chr12:30968314
|
T | A | 1 | a0002c0002t0004g0239 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.276+4297T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968314 | ||||||
| chr12:30968333
|
C | A | 5 | a0001c0001t0004g0009a0001c0001t0004g0011a0001c0001t0004g0214others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+4316C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968333 | ||||||
| chr12:30968411
|
C | T | 1 | a0001c0001t0004g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.276+4394C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968411 | ||||||
| chr12:30968415
|
G | A | 61 | a0001c0001t0001g0203a0001c0001t0001g0288a0001c0001t0002g0210others(58): Show | 62 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.276+4398G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968415 | ||||||
| chr12:30968637
|
G | A | 55 | a0001c0001t0001g0288a0001c0001t0002g0210a0001c0001t0002g0287others(52): Show | 56 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.276+4620G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968637 | ||||||
| chr12:30968661
|
T | G | 29 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0220others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.276+4644T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968661 | ||||||
| chr12:30968806
|
C | T | 10 | a0001c0001t0001g0342a0001c0001t0002g0002a0001c0001t0002g0077others(7): Show | 11 | HG00733.hp1 HG00735.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.276+4789C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968806 | ||||||
| chr12:30968928
|
G | A | 17 | a0001c0001t0002g0163a0001c0001t0002g0374a0001c0001t0002g0375others(14): Show | 17 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+4911G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968928 | ||||||
| chr12:30968933
|
A | G | 73 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(70): Show | 73 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.276+4916A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968933 | ||||||
| chr12:30968958
|
T | A | 1 | a0002c0002t0003g0168 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.276+4941T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30968958 | ||||||
| chr12:30969044
|
A | G | 1 | a0002c0002t0007g0141 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.276+5027A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969044 | ||||||
| chr12:30969095
|
C | A | 10 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0016g0365others(7): Show | 10 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.276+5078C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969095 | ||||||
| chr12:30969112
|
T | A | 10 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0016g0365others(7): Show | 10 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.276+5095T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969112 | ||||||
| chr12:30969149
|
G | C | 19 | a0002c0002t0018g0183a0003c0003t0001g0114a0003c0003t0003g0078others(16): Show | 19 | HG00673.hp1 HG02109.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.276+5132G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969149 | ||||||
| chr12:30969152
|
A | G | 105 | a0001c0001t0001g0099a0001c0001t0001g0244a0001c0001t0001g0245others(102): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.276+5135A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969152 | ||||||
| chr12:30969214
|
G | C | 4 | a0001c0001t0008g0058a0001c0001t0012g0164a0002c0002t0001g0031others(1): Show | 4 | HG02165.hp1 NA18985.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.276+5197G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969214 | ||||||
| chr12:30969281
|
T | C | 55 | a0001c0001t0001g0288a0001c0001t0002g0210a0001c0001t0002g0287others(52): Show | 56 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.276+5264T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969281 | ||||||
| chr12:30969314
|
T | C | 27 | a0001c0001t0001g0197a0001c0001t0002g0163a0001c0001t0002g0374others(24): Show | 27 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.276+5297T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969314 | ||||||
| chr12:30969366
|
A | G | 1 | a0001c0001t0009g0372 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.276+5349A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969366 | ||||||
| chr12:30969477
|
G | A | 1 | a0002c0002t0001g0081 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.276+5460G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969477 | ||||||
| chr12:30969534
|
C | T | 18 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(15): Show | 18 | HG00673.hp1 HG02132.hp1 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.276+5517C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969534 | ||||||
| chr12:30969539
|
T | C | 179 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(176): Show | 180 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.276+5522T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969539 | ||||||
| chr12:30969555
|
C | T | 4 | a0001c0001t0001g0197a0001c0001t0021g0198a0001c0001t0021g0212others(1): Show | 4 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+5538C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969555 | ||||||
| chr12:30969594
|
C | T | 10 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0016g0365others(7): Show | 10 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.276+5577C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969594 | ||||||
| chr12:30969631
|
C | G | 61 | a0001c0001t0001g0203a0001c0001t0001g0288a0001c0001t0002g0210others(58): Show | 62 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.276+5614C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969631 | ||||||
| chr12:30969669
|
C | T | 1 | a0001c0001t0006g0328 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.276+5652C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969669 | ||||||
| chr12:30969690
|
G | A | 17 | a0001c0001t0002g0163a0001c0001t0002g0374a0001c0001t0002g0375others(14): Show | 17 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+5673G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969690 | ||||||
| chr12:30969771
|
C | T | 104 | a0001c0001t0001g0099a0001c0001t0001g0244a0001c0001t0001g0245others(101): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.276+5754C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969771 | ||||||
| chr12:30969872
|
G | A | 10 | a0001c0001t0001g0197a0001c0001t0004g0186a0001c0001t0016g0365others(7): Show | 10 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.276+5855G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30969872 | ||||||
| chr12:30970022
|
C | T | 1 | a0001c0001t0069g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.276+6005C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970022 | ||||||
| chr12:30970107
|
A | C | 1 | a0001c0001t0001g0080 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.276+6090A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970107 | ||||||
| chr12:30970463
|
A | G | 2 | a0003c0003t0001g0114a0003c0003t0032g0241 | 2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.276+6446A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970463 | ||||||
| chr12:30970622
|
A | T | 82 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(79): Show | 82 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.276+6605A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970622 | ||||||
| chr12:30970641
|
C | T | 82 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(79): Show | 82 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.276+6624C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970641 | ||||||
| chr12:30970737
|
C | T | 117 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(114): Show | 117 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.276+6720C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970737 | ||||||
| chr12:30970915
|
T | C | 1 | a0002c0002t0001g0072 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.276+6898T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970915 | ||||||
| chr12:30970985
|
C | A | 20 | a0002c0002t0018g0038a0002c0002t0018g0183a0003c0003t0001g0114others(17): Show | 20 | HG00673.hp1 HG02109.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.276+6968C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30970985 | ||||||
| chr12:30971433
|
A | G | 70 | a0001c0001t0001g0099a0001c0001t0001g0257a0001c0001t0001g0342others(67): Show | 71 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.277-7128A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971433 | ||||||
| chr12:30971447
|
C | A | 15 | a0001c0001t0002g0163a0001c0001t0002g0374a0001c0001t0002g0375others(12): Show | 15 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.277-7114C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971447 | ||||||
| chr12:30971553
|
G | A | 73 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(70): Show | 73 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.277-7008G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971553 | ||||||
| chr12:30971633
|
C | T | 18 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(15): Show | 18 | HG00673.hp1 HG02132.hp1 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.277-6928C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971633 | ||||||
| chr12:30971655
|
T | G | 68 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0113others(65): Show | 68 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.277-6906T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971655 | ||||||
| chr12:30971682
|
C | T | 131 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0113others(128): Show | 133 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.277-6879C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971682 | ||||||
| chr12:30971724
|
A | T | 1 | a0002c0002t0014g0124 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.277-6837A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971724 | ||||||
| chr12:30971749
|
CA | C | 92 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(89): Show | 92 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.277-6801delA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30971749 | |||||
| chr12:30971843
|
T | TA | 132 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0113others(129): Show | 134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.277-6705dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30971843 | |||||
| chr12:30971843
|
TA | T | 157 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(154): Show | 158 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.277-6705delA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30971843 | |||||
| chr12:30971880
|
T | C | 1 | a0002c0004t0014g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.277-6681T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30971880 | ||||||
| chr12:30972064
|
T | C | 3 | a0001c0001t0002g0233a0001c0001t0004g0277a0001c0001t0009g0271 | 3 | HG00733.hp2 HG01192.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.277-6497T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972064 | ||||||
| chr12:30972768
|
C | T | 1 | a0002c0002t0001g0039 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.277-5793C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972768 | ||||||
| chr12:30972795
|
C | T | 15 | a0003c0003t0001g0114a0003c0003t0003g0078a0003c0003t0005g0054others(12): Show | 15 | HG00673.hp1 HG02132.hp1 HG02683.hp1 others(12): Show |
intron_variant | MODIFIER | c.277-5766C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972795 | ||||||
| chr12:30972807
|
G | A | 2 | a0001c0001t0019g0388a0001c0001t0019g0389 | 2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.277-5754G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972807 | ||||||
| chr12:30972899
|
G | A | 78 | a0001c0001t0001g0099a0001c0001t0001g0257a0001c0001t0001g0342others(75): Show | 79 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.277-5662G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972899 | ||||||
| chr12:30972910
|
C | T | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.277-5651C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972910 | ||||||
| chr12:30972916
|
G | A | 2 | a0001c0001t0001g0020a0002c0002t0018g0201 | 2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.277-5645G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972916 | ||||||
| chr12:30972997
|
C | T | 14 | a0001c0001t0020g0024a0002c0002t0001g0142a0002c0002t0005g0130others(11): Show | 15 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.277-5564C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30972997 | ||||||
| chr12:30973055
|
T | C | 1 | a0002c0002t0001g0142 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.277-5506T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973055 | ||||||
| chr12:30973085
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.277-5476C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973085 | ||||||
| chr12:30973248
|
G | A | 1 | a0002c0002t0004g0096 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.277-5313G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973248 | ||||||
| chr12:30973280
|
T | A | 2 | a0001c0001t0051g0177a0002c0002t0004g0295 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.277-5281T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973280 | ||||||
| chr12:30973305
|
C | T | 16 | a0001c0001t0001g0043a0001c0001t0001g0154a0001c0001t0001g0169others(13): Show | 16 | HG00558.hp2 HG01099.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.277-5256C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973305 | ||||||
| chr12:30973499
|
G | A | 1 | a0001c0001t0010g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.277-5062G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973499 | ||||||
| chr12:30973524
|
C | T | 8 | a0001c0001t0014g0369a0001c0001t0014g0387a0001c0001t0051g0177others(5): Show | 9 | HG02622.hp1 HG02886.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.277-5037C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973524 | ||||||
| chr12:30973590
|
T | TG | 5 | a0001c0001t0003g0098a0001c0001t0008g0093a0001c0001t0011g0097others(2): Show | 5 | HG02148.hp2 NA18998.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-4967dupG | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30973590 | |||||
| chr12:30973667
|
C | T | 3 | a0002c0002t0004g0021a0002c0002t0030g0308a0002c0004t0017g0003 | 4 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-4894C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973667 | ||||||
| chr12:30973745
|
T | C | 85 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0086others(82): Show | 85 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.277-4816T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973745 | ||||||
| chr12:30973860
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0018g0352 | 3 | HG03098.hp1 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.277-4701C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973860 | ||||||
| chr12:30973982
|
G | C | 3 | a0001c0001t0010g0209a0001c0001t0031g0102a0001c0001t0031g0207 | 3 | HG01928.hp2 HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.277-4579G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30973982 | ||||||
| chr12:30974016
|
C | T | 2 | a0001c0001t0025g0205a0001c0001t0025g0219 | 2 | HG01123.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.277-4545C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974016 | ||||||
| chr12:30974164
|
C | T | 50 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(47): Show | 51 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.277-4397C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974164 | ||||||
| chr12:30974170
|
C | T | 51 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(48): Show | 52 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.277-4391C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974170 | ||||||
| chr12:30974225
|
A | G | 84 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0351others(81): Show | 84 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.277-4336A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974225 | ||||||
| chr12:30974228
|
C | T | 14 | a0002c0002t0001g0142a0002c0002t0003g0121a0002c0002t0005g0130others(11): Show | 15 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.277-4333C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974228 | ||||||
| chr12:30974229
|
G | A | 14 | a0001c0001t0024g0180a0001c0001t0028g0181a0001c0001t0028g0316others(11): Show | 15 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.277-4332G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974229 | ||||||
| chr12:30974256
|
G | A | 3 | a0002c0002t0004g0318a0002c0002t0026g0281a0002c0002t0046g0188 | 3 | HG02886.hp2 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.277-4305G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974256 | ||||||
| chr12:30974309
|
A | G | 66 | a0001c0001t0001g0099a0001c0001t0001g0112a0001c0001t0002g0049others(63): Show | 66 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.277-4252A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974309 | ||||||
| chr12:30974336
|
G | A | 1 | a0001c0001t0011g0065 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.277-4225G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974336 | ||||||
| chr12:30974380
|
C | T | 4 | a0002c0005t0004g0004a0002c0005t0004g0361a0002c0005t0004g0362others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-4181C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974380 | ||||||
| chr12:30974385
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.277-4176C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974385 | ||||||
| chr12:30974559
|
A | G | 2 | a0001c0001t0002g0087a0001c0001t0004g0079 | 2 | HG01433.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.277-4002A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974559 | ||||||
| chr12:30974592
|
G | A | 2 | a0001c0001t0005g0301a0001c0001t0017g0302 | 2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.277-3969G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974592 | ||||||
| chr12:30974598
|
A | G | 6 | a0001c0001t0001g0351a0001c0001t0001g0353a0001c0001t0004g0009others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-3963A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974598 | ||||||
| chr12:30974718
|
G | A | 1 | a0002c0002t0004g0239 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.277-3843G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974718 | ||||||
| chr12:30974786
|
G | A | 1 | a0002c0002t0015g0385 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.277-3775G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974786 | ||||||
| chr12:30974809
|
C | T | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.277-3752C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974809 | ||||||
| chr12:30974823
|
A | G | 1 | a0002c0002t0001g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.277-3738A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974823 | ||||||
| chr12:30974824
|
G | A | 1 | a0002c0002t0001g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.277-3737G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974824 | ||||||
| chr12:30974865
|
G | A | 1 | a0002c0002t0047g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.277-3696G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974865 | ||||||
| chr12:30974909
|
C | T | 1 | a0010c0012t0050g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.277-3652C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974909 | ||||||
| chr12:30974986
|
C | T | 2 | a0001c0001t0002g0374a0001c0001t0002g0375 | 2 | HG00438.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.277-3575C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30974986 | ||||||
| chr12:30975081
|
G | A | 64 | a0001c0001t0001g0257a0001c0001t0001g0288a0001c0001t0001g0342others(61): Show | 65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.277-3480G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975081 | ||||||
| chr12:30975155
|
G | A | 1 | a0002c0002t0038g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277-3406G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975155 | ||||||
| chr12:30975164
|
G | A | 1 | a0002c0002t0001g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.277-3397G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975164 | ||||||
| chr12:30975397
|
G | A | 1 | a0001c0001t0034g0228 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.277-3164G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975397 | ||||||
| chr12:30975493
|
G | A | 1 | a0001c0001t0028g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.277-3068G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975493 | ||||||
| chr12:30975496
|
A | G | 1 | a0001c0001t0002g0347 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.277-3065A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975496 | ||||||
| chr12:30975656
|
C | T | 3 | a0001c0001t0019g0388a0001c0001t0019g0389a0012c0014t0019g0125 | 3 | HG03486.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.277-2905C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975656 | ||||||
| chr12:30975658
|
A | C | 46 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(43): Show | 47 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.277-2903A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975658 | ||||||
| chr12:30975663
|
G | A | 1 | a0002c0002t0001g0069 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.277-2898G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975663 | ||||||
| chr12:30975671
|
T | C | 375 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(372): Show | 378 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.277-2890T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975671 | ||||||
| chr12:30975742
|
C | G | 7 | a0001c0001t0001g0107a0001c0001t0002g0350a0001c0001t0012g0032others(4): Show | 7 | HG02083.hp1 HG02135.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-2819C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975742 | ||||||
| chr12:30975884
|
G | A | 1 | a0002c0002t0001g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.277-2677G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975884 | ||||||
| chr12:30975885
|
A | G | 1 | a0002c0002t0001g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.277-2676A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975885 | ||||||
| chr12:30975886
|
G | C | 1 | a0002c0002t0001g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.277-2675G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975886 | ||||||
| chr12:30975913
|
T | C | 2 | a0001c0001t0002g0220a0001c0001t0002g0269 | 2 | HG00280.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.277-2648T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975913 | ||||||
| chr12:30975985
|
G | A | 65 | a0001c0001t0001g0257a0001c0001t0001g0288a0001c0001t0001g0342others(62): Show | 66 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.277-2576G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30975985 | ||||||
| chr12:30976011
|
A | G | 134 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0257others(131): Show | 135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.277-2550A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976011 | ||||||
| chr12:30976024
|
G | A | 2 | a0001c0001t0003g0266a0008c0011t0002g0260 | 2 | HG00423.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.277-2537G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976024 | ||||||
| chr12:30976037
|
G | C | 14 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0351others(11): Show | 14 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.277-2524G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976037 | ||||||
| chr12:30976053
|
G | A | 120 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0101others(117): Show | 121 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.277-2508G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976053 | ||||||
| chr12:30976195
|
G | A | 21 | a0001c0001t0002g0376a0001c0001t0004g0186a0001c0001t0005g0313others(18): Show | 21 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.277-2366G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976195 | ||||||
| chr12:30976232
|
G | A | 1 | a0002c0002t0073g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.277-2329G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976232 | ||||||
| chr12:30976240
|
C | T | 43 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0101others(40): Show | 43 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.277-2321C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976240 | ||||||
| chr12:30976245
|
T | G | 1 | a0002c0002t0026g0281 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.277-2316T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976245 | ||||||
| chr12:30976302
|
C | T | 1 | a0001c0001t0037g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.277-2259C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976302 | ||||||
| chr12:30976424
|
G | T | 15 | a0002c0002t0001g0142a0002c0002t0003g0121a0002c0002t0005g0130others(12): Show | 16 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.277-2137G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976424 | ||||||
| chr12:30976509
|
A | G | 377 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(374): Show | 380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.277-2052A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976509 | ||||||
| chr12:30976636
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.277-1925A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976636 | ||||||
| chr12:30976658
|
C | T | 297 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(294): Show | 299 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.277-1903C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976658 | ||||||
| chr12:30976659
|
A | G | 377 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(374): Show | 380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.277-1902A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976659 | ||||||
| chr12:30976689
|
G | A | 6 | a0001c0001t0002g0363a0001c0001t0022g0051a0001c0001t0056g0358others(3): Show | 6 | HG02145.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-1872G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976689 | ||||||
| chr12:30976740
|
G | A | 4 | a0001c0001t0001g0288a0001c0001t0002g0286a0001c0001t0002g0296others(1): Show | 4 | HG00735.hp1 HG03491.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-1821G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976740 | ||||||
| chr12:30976961
|
T | C | 76 | a0001c0001t0001g0099a0001c0001t0001g0112a0001c0001t0001g0197others(73): Show | 76 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.277-1600T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976961 | ||||||
| chr12:30976969
|
G | A | 1 | a0001c0001t0002g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.277-1592G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30976969 | ||||||
| chr12:30977098
|
A | T | 2 | a0001c0001t0022g0051a0001c0001t0056g0358 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.277-1463A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977098 | ||||||
| chr12:30977164
|
G | A | 1 | a0002c0002t0072g0153 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.277-1397G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977164 | ||||||
| chr12:30977232
|
A | G | 1 | a0002c0002t0046g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.277-1329A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977232 | ||||||
| chr12:30977291
|
G | A | 1 | a0002c0002t0026g0299 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.277-1270G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977291 | ||||||
| chr12:30977296
|
G | GCCGCCAC | 8 | a0001c0001t0002g0376a0001c0001t0005g0313a0001c0001t0005g0377others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.277-1256_277-1250d others(9): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30977296 | |||||
| chr12:30977314
|
A | G | 37 | a0001c0001t0002g0123a0001c0001t0002g0359a0001c0001t0005g0122others(34): Show | 37 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.277-1247A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977314 | ||||||
| chr12:30977319
|
C | T | 378 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(375): Show | 381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.277-1242C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977319 | ||||||
| chr12:30977370
|
C | T | 1 | a0002c0002t0001g0035 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.277-1191C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977370 | ||||||
| chr12:30977406
|
C | T | 1 | a0002c0002t0001g0068 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.277-1155C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977406 | ||||||
| chr12:30977415
|
C | T | 214 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(211): Show | 216 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.277-1146C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977415 | ||||||
| chr12:30977440
|
G | A | 1 | a0002c0002t0026g0025 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.277-1121G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977440 | ||||||
| chr12:30977472
|
G | T | 1 | a0001c0001t0059g0332 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.277-1089G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977472 | ||||||
| chr12:30977502
|
C | A | 9 | a0002c0002t0002g0174a0002c0002t0002g0175a0002c0002t0002g0184others(6): Show | 9 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.277-1059C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977502 | ||||||
| chr12:30977506
|
C | T | 1 | a0002c0002t0045g0037 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.277-1055C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977506 | ||||||
| chr12:30977532
|
G | GCTCCCCC others(3): Show |
8 | a0001c0001t0002g0376a0001c0001t0005g0313a0001c0001t0005g0377others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.277-1024_277-1015d others(12): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 30977532 | |||||
| chr12:30977566
|
C | T | 118 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0101others(115): Show | 119 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.277-995C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977566 | ||||||
| chr12:30977745
|
G | A | 1 | a0001c0001t0010g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.277-816G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977745 | ||||||
| chr12:30977868
|
T | C | 1 | a0002c0002t0038g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277-693T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977868 | ||||||
| chr12:30977897
|
A | C | 1 | a0001c0001t0005g0381 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.277-664A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977897 | ||||||
| chr12:30977937
|
C | G | 9 | a0002c0002t0002g0174a0002c0002t0002g0175a0002c0002t0002g0184others(6): Show | 9 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.277-624C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977937 | ||||||
| chr12:30977969
|
G | A | 8 | a0001c0001t0002g0376a0001c0001t0005g0313a0001c0001t0005g0377others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.277-592G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30977969 | ||||||
| chr12:30978047
|
G | A | 1 | a0002c0004t0001g0234 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.277-514G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978047 | ||||||
| chr12:30978104
|
T | C | 1 | a0002c0002t0002g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.277-457T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978104 | ||||||
| chr12:30978137
|
G | A | 1 | a0010c0012t0050g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.277-424G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978137 | ||||||
| chr12:30978137
|
G | C | 73 | a0001c0001t0001g0099a0001c0001t0001g0107a0001c0001t0001g0112others(70): Show | 73 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.277-424G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978137 | ||||||
| chr12:30978277
|
G | C | 1 | a0001c0001t0004g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.277-284G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978277 | ||||||
| chr12:30978388
|
G | C | 1 | a0010c0012t0050g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.277-173G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978388 | ||||||
| chr12:30978414
|
C | T | 1 | a0006c0013t0011g0338 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.277-147C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 3/7 | chr12 | 30978414 | ||||||
| chr12:30978689
|
G | A | 1 | a0002c0004t0014g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.351+54G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30978689 | ||||||
| chr12:30978777
|
T | C | 349 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(346): Show | 351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.351+142T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30978777 | ||||||
| chr12:30978782
|
G | A | 3 | a0002c0002t0014g0279a0002c0002t0021g0034a0002c0002t0045g0037 | 3 | HG02723.hp2 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.351+147G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30978782 | ||||||
| chr12:30978863
|
C | T | 23 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(20): Show | 23 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.351+228C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30978863 | ||||||
| chr12:30978918
|
G | T | 1 | a0010c0012t0050g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.351+283G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30978918 | ||||||
| chr12:30978941
|
A | G | 15 | a0002c0002t0001g0142a0002c0002t0003g0121a0002c0002t0005g0130others(12): Show | 16 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.351+306A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30978941 | ||||||
| chr12:30979081
|
G | A | 1 | a0002c0002t0007g0251 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.351+446G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979081 | ||||||
| chr12:30979089
|
G | A | 55 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0002g0049others(52): Show | 55 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.351+454G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979089 | ||||||
| chr12:30979125
|
C | G | 30 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(27): Show | 30 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.352-441C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979125 | ||||||
| chr12:30979131
|
G | A | 64 | a0001c0001t0001g0257a0001c0001t0001g0288a0001c0001t0001g0342others(61): Show | 65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.352-435G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979131 | ||||||
| chr12:30979248
|
T | G | 2 | a0002c0002t0001g0081a0002c0002t0001g0082 | 2 | NA18946.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.352-318T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979248 | ||||||
| chr12:30979308
|
T | A | 65 | a0001c0001t0001g0257a0001c0001t0001g0288a0001c0001t0001g0342others(62): Show | 66 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.352-258T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979308 | ||||||
| chr12:30979356
|
G | A | 1 | a0001c0001t0014g0369 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.352-210G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979356 | ||||||
| chr12:30979422
|
T | TA | 30 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(27): Show | 30 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.352-143dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 30979422 | |||||
| chr12:30979450
|
C | A | 12 | a0001c0001t0004g0186a0001c0001t0015g0366a0001c0001t0015g0367others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-116C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979450 | ||||||
| chr12:30979462
|
C | T | 3 | a0001c0001t0015g0366a0001c0001t0015g0367a0001c0001t0015g0370 | 3 | HG01192.hp1 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.352-104C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979462 | ||||||
| chr12:30979484
|
G | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0203 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.352-82G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979484 | ||||||
| chr12:30979526
|
C | T | 2 | a0001c0007t0013g0243a0001c0007t0013g0249 | 2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.352-40C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979526 | ||||||
| chr12:30979544
|
A | C | 361 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(358): Show | 363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.352-22A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979544 | ||||||
| chr12:30979549
|
G | C | 1 | a0001c0001t0001g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.352-17G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 4/7 | chr12 | 30979549 | ||||||
| chr12:30979725
|
G | A | 9 | a0002c0002t0002g0174a0002c0002t0002g0175a0002c0002t0002g0184others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.456+55G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30979725 | ||||||
| chr12:30979940
|
G | T | 157 | a0001c0001t0001g0099a0001c0001t0001g0107a0001c0001t0001g0112others(154): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.456+270G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30979940 | ||||||
| chr12:30979957
|
G | T | 12 | a0001c0001t0002g0363a0002c0002t0002g0174a0002c0002t0002g0175others(9): Show | 12 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.456+287G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30979957 | ||||||
| chr12:30979967
|
C | T | 4 | a0001c0001t0015g0366a0001c0001t0015g0367a0001c0001t0015g0368others(1): Show | 4 | HG01192.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+297C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30979967 | ||||||
| chr12:30980039
|
C | T | 73 | a0001c0001t0044g0317a0002c0002t0001g0031a0002c0002t0001g0035others(70): Show | 74 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.456+369C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980039 | ||||||
| chr12:30980108
|
C | T | 172 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0099others(169): Show | 173 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.456+438C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980108 | ||||||
| chr12:30980130
|
C | T | 167 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0099others(164): Show | 167 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.456+460C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980130 | ||||||
| chr12:30980204
|
C | A | 11 | a0002c0002t0002g0174a0002c0002t0002g0175a0002c0002t0002g0184others(8): Show | 11 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.456+534C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980204 | ||||||
| chr12:30980287
|
C | T | 1 | a0002c0002t0047g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456+617C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980287 | ||||||
| chr12:30980316
|
T | C | 377 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(374): Show | 380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.456+646T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980316 | ||||||
| chr12:30980484
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.456+814C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980484 | ||||||
| chr12:30980485
|
G | A | 226 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0099others(223): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.456+815G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980485 | ||||||
| chr12:30980552
|
C | T | 15 | a0002c0002t0001g0142a0002c0002t0003g0121a0002c0002t0005g0130others(12): Show | 16 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.456+882C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980552 | ||||||
| chr12:30980565
|
C | T | 1 | a0002c0002t0047g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456+895C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980565 | ||||||
| chr12:30980590
|
G | A | 1 | a0001c0001t0005g0301 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.456+920G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980590 | ||||||
| chr12:30980719
|
T | G | 261 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.456+1049T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980719 | ||||||
| chr12:30980720
|
C | A | 261 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(258): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.456+1050C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980720 | ||||||
| chr12:30980729
|
T | C | 227 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0099others(224): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.456+1059T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980729 | ||||||
| chr12:30980814
|
A | G | 1 | a0002c0002t0024g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.456+1144A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980814 | ||||||
| chr12:30980885
|
C | T | 225 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0099others(222): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.456+1215C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980885 | ||||||
| chr12:30980961
|
G | A | 1 | a0001c0001t0020g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.456+1291G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980961 | ||||||
| chr12:30980966
|
G | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0002g0350others(3): Show | 6 | HG00673.hp1 HG02602.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.456+1296G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30980966 | ||||||
| chr12:30980993
|
CAG | C | 14 | a0001c0001t0002g0376a0001c0001t0005g0104a0001c0001t0005g0118others(11): Show | 14 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.456+1325_456+1326d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 30980993 | |||||
| chr12:30981040
|
G | A | 1 | a0001c0001t0008g0090 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.456+1370G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981040 | ||||||
| chr12:30981128
|
A | G | 270 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(267): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.457-1404A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981128 | ||||||
| chr12:30981133
|
C | T | 84 | a0001c0001t0044g0317a0002c0002t0001g0031a0002c0002t0001g0035others(81): Show | 85 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.457-1399C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981133 | ||||||
| chr12:30981167
|
G | C | 3 | a0001c0001t0004g0006a0001c0001t0014g0369a0001c0001t0014g0387 | 3 | HG02896.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.457-1365G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981167 | ||||||
| chr12:30981208
|
A | G | 371 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(368): Show | 374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.457-1324A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981208 | ||||||
| chr12:30981230
|
G | A | 221 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0099others(218): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.457-1302G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981230 | ||||||
| chr12:30981236
|
G | T | 73 | a0001c0001t0044g0317a0002c0002t0001g0031a0002c0002t0001g0035others(70): Show | 74 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.457-1296G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981236 | ||||||
| chr12:30981251
|
C | T | 1 | a0002c0002t0025g0139 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.457-1281C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981251 | ||||||
| chr12:30981367
|
T | C | 256 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(253): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.457-1165T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981367 | ||||||
| chr12:30981501
|
CAG | C | 3 | a0001c0001t0010g0209a0001c0001t0031g0102a0001c0001t0031g0207 | 3 | HG01928.hp2 HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.457-1028_457-1027d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 30981501 | |||||
| chr12:30981536
|
CCTT | C | 11 | a0002c0002t0002g0174a0002c0002t0002g0175a0002c0002t0002g0184others(8): Show | 11 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.457-993_457-991del others(3): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 30981536 | |||||
| chr12:30981546
|
G | A | 3 | a0001c0001t0004g0006a0001c0001t0014g0369a0001c0001t0014g0387 | 3 | HG02896.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.457-986G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981546 | ||||||
| chr12:30981573
|
GTCATGCT others(4): Show |
G | 48 | a0002c0002t0001g0031a0002c0002t0001g0035a0002c0002t0001g0036others(45): Show | 48 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.457-956_457-946del others(11): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 30981573 | |||||
| chr12:30981579
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.457-953C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981579 | ||||||
| chr12:30981623
|
C | T | 1 | a0002c0002t0004g0239 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.457-909C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981623 | ||||||
| chr12:30981691
|
C | T | 372 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(369): Show | 375 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.457-841C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981691 | ||||||
| chr12:30981696
|
G | A | 1 | a0002c0002t0015g0385 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.457-836G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981696 | ||||||
| chr12:30981767
|
T | C | 1 | a0001c0001t0014g0369 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.457-765T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981767 | ||||||
| chr12:30981897
|
C | T | 1 | a0002c0002t0030g0308 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.457-635C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981897 | ||||||
| chr12:30981974
|
C | T | 1 | a0002c0004t0017g0152 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.457-558C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30981974 | ||||||
| chr12:30982019
|
C | T | 2 | a0001c0001t0029g0192a0001c0001t0029g0193 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.457-513C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30982019 | ||||||
| chr12:30982244
|
G | A | 36 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(33): Show | 36 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.457-288G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30982244 | ||||||
| chr12:30982250
|
C | T | 2 | a0001c0001t0020g0017a0001c0001t0020g0018 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.457-282C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30982250 | ||||||
| chr12:30982469
|
C | G | 1 | a0001c0001t0005g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.457-63C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30982469 | ||||||
| chr12:30982483
|
C | A | 51 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(48): Show | 51 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.457-49C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30982483 | ||||||
| chr12:30982487
|
C | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0002g0350others(3): Show | 6 | HG00673.hp1 HG02602.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-45C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 5/7 | chr12 | 30982487 | ||||||
| chr12:30982740
|
C | T | 1 | a0002c0004t0053g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615+50C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982740 | ||||||
| chr12:30982778
|
G | A | 1 | a0001c0001t0037g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.615+88G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982778 | ||||||
| chr12:30982781
|
T | C | 2 | a0001c0007t0013g0243a0001c0007t0013g0249 | 2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.615+91T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982781 | ||||||
| chr12:30982814
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0235 | 2 | NA18945.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.615+124C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982814 | ||||||
| chr12:30982832
|
G | T | 1 | a0005c0017t0011g0171 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.615+142G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982832 | ||||||
| chr12:30982871
|
T | C | 20 | a0002c0002t0001g0142a0002c0002t0003g0121a0002c0002t0005g0130others(17): Show | 21 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.615+181T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982871 | ||||||
| chr12:30982970
|
A | T | 253 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(250): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.616-94A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982970 | ||||||
| chr12:30982990
|
G | A | 33 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(30): Show | 33 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.616-74G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30982990 | ||||||
| chr12:30983000
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0022g0179 | 2 | HG02055.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.616-64G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 6/7 | chr12 | 30983000 | ||||||
| chr12:30983165
|
G | A | 2 | a0001c0001t0003g0041a0001c0001t0003g0083 | 2 | HG00558.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.702+15G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983165 | ||||||
| chr12:30983217
|
C | T | 1 | a0001c0001t0005g0118 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.702+67C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983217 | ||||||
| chr12:30983259
|
C | A | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.702+109C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983259 | ||||||
| chr12:30983261
|
C | G | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.702+111C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983261 | ||||||
| chr12:30983262
|
G | C | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.702+112G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983262 | ||||||
| chr12:30983292
|
C | T | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.702+142C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983292 | ||||||
| chr12:30983321
|
C | T | 84 | a0002c0002t0001g0031a0002c0002t0001g0035a0002c0002t0001g0036others(81): Show | 85 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.702+171C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983321 | ||||||
| chr12:30983384
|
A | G | 37 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(34): Show | 37 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.702+234A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983384 | ||||||
| chr12:30983433
|
C | A | 48 | a0002c0002t0001g0031a0002c0002t0001g0035a0002c0002t0001g0036others(45): Show | 48 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.702+283C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983433 | ||||||
| chr12:30983480
|
C | T | 34 | a0001c0001t0002g0376a0001c0001t0005g0104a0001c0001t0005g0118others(31): Show | 35 | HG00438.hp2 HG01257.hp2 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.702+330C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983480 | ||||||
| chr12:30983521
|
A | G | 1 | a0010c0012t0050g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702+371A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983521 | ||||||
| chr12:30983755
|
C | T | 3 | a0001c0001t0005g0377a0001c0001t0005g0378a0001c0001t0005g0380 | 3 | HG01257.hp2 HG01258.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.702+605C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983755 | ||||||
| chr12:30983763
|
T | C | 3 | a0001c0001t0004g0006a0001c0001t0014g0369a0001c0001t0014g0387 | 3 | HG02896.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.702+613T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983763 | ||||||
| chr12:30983815
|
A | T | 14 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0351others(11): Show | 14 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.702+665A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983815 | ||||||
| chr12:30983825
|
T | A | 37 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(34): Show | 37 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.702+675T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983825 | ||||||
| chr12:30983898
|
T | C | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.702+748T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983898 | ||||||
| chr12:30983936
|
A | T | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.702+786A>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983936 | ||||||
| chr12:30983983
|
T | G | 3 | a0001c0001t0004g0006a0001c0001t0014g0369a0001c0001t0014g0387 | 3 | HG02896.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.702+833T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30983983 | ||||||
| chr12:30984068
|
G | A | 1 | a0002c0002t0001g0199 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.702+918G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984068 | ||||||
| chr12:30984089
|
G | T | 1 | a0002c0004t0005g0246 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.702+939G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984089 | ||||||
| chr12:30984094
|
G | A | 216 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0099others(213): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.702+944G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984094 | ||||||
| chr12:30984116
|
C | T | 73 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0101others(70): Show | 73 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.702+966C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984116 | ||||||
| chr12:30984123
|
G | A | 20 | a0002c0002t0001g0142a0002c0002t0003g0121a0002c0002t0005g0130others(17): Show | 21 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.702+973G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984123 | ||||||
| chr12:30984124
|
C | T | 8 | a0001c0001t0003g0094a0001c0001t0003g0098a0001c0001t0003g0110others(5): Show | 8 | HG04184.hp1 NA18956.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.702+974C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984124 | ||||||
| chr12:30984132
|
C | T | 51 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0002g0049others(48): Show | 51 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.702+982C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984132 | ||||||
| chr12:30984205
|
G | A | 216 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0099others(213): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.702+1055G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984205 | ||||||
| chr12:30984261
|
T | G | 254 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(251): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.702+1111T>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984261 | ||||||
| chr12:30984377
|
C | A | 29 | a0001c0001t0002g0123a0001c0001t0002g0359a0001c0001t0005g0301others(26): Show | 29 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.702+1227C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984377 | ||||||
| chr12:30984544
|
G | A | 1 | a0001c0001t0005g0380 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.702+1394G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984544 | ||||||
| chr12:30984552
|
C | CT | 72 | a0001c0001t0002g0049a0001c0001t0002g0363a0001c0001t0003g0094others(69): Show | 72 | HG00642.hp2 HG00673.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.702+1426dupT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30984552 | |||||
| chr12:30984552
|
C | CTT | 37 | a0001c0001t0001g0113a0001c0001t0001g0240a0001c0001t0001g0262others(34): Show | 38 | HG00438.hp2 HG02015.hp1 HG02015.hp2 others(35): Show |
intron_variant | MODIFIER | c.702+1425_702+1426d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30984552 | |||||
| chr12:30984552
|
C | CTTT | 49 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(46): Show | 49 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.702+1424_702+1426d others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30984552 | |||||
| chr12:30984552
|
C | CTTTT | 21 | a0001c0001t0001g0056a0001c0001t0001g0146a0001c0001t0001g0292others(18): Show | 21 | HG00438.hp1 HG00673.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.702+1423_702+1426d others(6): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30984552 | |||||
| chr12:30984552
|
CT | C | 54 | a0001c0001t0001g0288a0001c0001t0001g0342a0001c0001t0002g0002others(51): Show | 55 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.702+1426delT | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30984552 | |||||
| chr12:30984552
|
CTTT | C | 11 | a0002c0002t0002g0174a0002c0002t0002g0175a0002c0002t0002g0184others(8): Show | 11 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.702+1424_702+1426d others(5): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30984552 | |||||
| chr12:30984833
|
T | C | 372 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(369): Show | 375 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.702+1683T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984833 | ||||||
| chr12:30984873
|
C | T | 1 | a0010c0012t0050g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702+1723C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984873 | ||||||
| chr12:30984907
|
A | C | 1 | a0001c0001t0001g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.702+1757A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984907 | ||||||
| chr12:30984967
|
C | T | 43 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0101others(40): Show | 43 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.702+1817C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984967 | ||||||
| chr12:30984968
|
C | T | 19 | a0002c0002t0001g0142a0002c0002t0003g0121a0002c0002t0005g0130others(16): Show | 20 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.702+1818C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30984968 | ||||||
| chr12:30985070
|
T | A | 1 | a0001c0001t0003g0320 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.702+1920T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985070 | ||||||
| chr12:30985132
|
G | C | 20 | a0002c0002t0001g0142a0002c0002t0003g0121a0002c0002t0005g0130others(17): Show | 21 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.702+1982G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985132 | ||||||
| chr12:30985145
|
C | T | 1 | a0002c0002t0018g0038 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.702+1995C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985145 | ||||||
| chr12:30985194
|
C | G | 1 | a0001c0001t0056g0358 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.702+2044C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985194 | ||||||
| chr12:30985242
|
T | C | 5 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0002g0350others(2): Show | 5 | HG02602.hp2 HG02683.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+2092T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985242 | ||||||
| chr12:30985383
|
G | A | 221 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0101others(218): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.702+2233G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985383 | ||||||
| chr12:30985522
|
T | C | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.702+2372T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985522 | ||||||
| chr12:30985662
|
G | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0356others(1): Show | 4 | HG03130.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+2512G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985662 | ||||||
| chr12:30985777
|
G | A | 1 | a0001c0001t0003g0225 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.702+2627G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985777 | ||||||
| chr12:30985874
|
A | C | 370 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(367): Show | 373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.702+2724A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985874 | ||||||
| chr12:30985932
|
C | T | 1 | a0001c0001t0011g0065 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.702+2782C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985932 | ||||||
| chr12:30985999
|
G | T | 2 | a0002c0002t0004g0182a0002c0002t0004g0295 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.702+2849G>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30985999 | ||||||
| chr12:30986282
|
T | C | 1 | a0002c0002t0026g0281 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.702+3132T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986282 | ||||||
| chr12:30986325
|
G | A | 14 | a0001c0001t0002g0376a0001c0001t0005g0104a0001c0001t0005g0118others(11): Show | 14 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.702+3175G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986325 | ||||||
| chr12:30986334
|
C | T | 35 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(32): Show | 35 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.702+3184C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986334 | ||||||
| chr12:30986366
|
T | C | 189 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0099others(186): Show | 190 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.702+3216T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986366 | ||||||
| chr12:30986447
|
T | C | 1 | a0001c0001t0002g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.702+3297T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986447 | ||||||
| chr12:30986489
|
C | T | 5 | a0002c0004t0014g0195a0002c0005t0004g0004a0002c0005t0004g0361others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+3339C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986489 | ||||||
| chr12:30986514
|
G | C | 1 | a0002c0002t0005g0312 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.702+3364G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986514 | ||||||
| chr12:30986662
|
C | T | 15 | a0001c0001t0002g0376a0001c0001t0005g0104a0001c0001t0005g0118others(12): Show | 15 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3512C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986662 | ||||||
| chr12:30986751
|
A | G | 86 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(83): Show | 87 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.702+3601A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986751 | ||||||
| chr12:30986759
|
A | G | 1 | a0001c0001t0002g0359 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.702+3609A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986759 | ||||||
| chr12:30986784
|
G | C | 15 | a0001c0001t0002g0376a0001c0001t0005g0104a0001c0001t0005g0118others(12): Show | 15 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3634G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986784 | ||||||
| chr12:30986876
|
G | A | 2 | a0001c0008t0001g0045a0001c0008t0001g0046 | 2 | HG02083.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.702+3726G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986876 | ||||||
| chr12:30986892
|
C | T | 1 | a0002c0002t0045g0037 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.702+3742C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986892 | ||||||
| chr12:30986968
|
A | G | 3 | a0001c0001t0004g0006a0001c0001t0014g0369a0001c0001t0014g0387 | 3 | HG02896.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.702+3818A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30986968 | ||||||
| chr12:30987030
|
G | A | 15 | a0001c0001t0002g0376a0001c0001t0005g0104a0001c0001t0005g0118others(12): Show | 15 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3880G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987030 | ||||||
| chr12:30987031
|
T | C | 9 | a0002c0002t0002g0174a0002c0002t0002g0175a0002c0002t0002g0184others(6): Show | 9 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+3881T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987031 | ||||||
| chr12:30987180
|
G | A | 176 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0099others(173): Show | 177 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.702+4030G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987180 | ||||||
| chr12:30987267
|
C | T | 15 | a0001c0001t0002g0376a0001c0001t0005g0104a0001c0001t0005g0118others(12): Show | 15 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+4117C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987267 | ||||||
| chr12:30987272
|
G | A | 4 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0073others(1): Show | 4 | HG01943.hp1 NA18977.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+4122G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987272 | ||||||
| chr12:30987283
|
G | C | 1 | a0001c0001t0004g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.702+4133G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987283 | ||||||
| chr12:30987344
|
C | A | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.702+4194C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987344 | ||||||
| chr12:30987383
|
T | C | 2 | a0002c0002t0012g0237a0002c0002t0012g0384 | 2 | NA18945.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.702+4233T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987383 | ||||||
| chr12:30987623
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.703-4233A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987623 | ||||||
| chr12:30987688
|
A | C | 1 | a0002c0002t0001g0081 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.703-4168A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987688 | ||||||
| chr12:30987861
|
C | T | 1 | a0007c0009t0001g0055 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.703-3995C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987861 | ||||||
| chr12:30987910
|
C | CA | 275 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(272): Show | 277 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.703-3945dupA | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30987910 | |||||
| chr12:30987953
|
A | G | 1 | a0001c0001t0040g0255 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.703-3903A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987953 | ||||||
| chr12:30987985
|
C | T | 20 | a0002c0002t0001g0142a0002c0002t0003g0121a0002c0002t0005g0130others(17): Show | 21 | HG00438.hp2 HG02080.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.703-3871C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30987985 | ||||||
| chr12:30988075
|
A | C | 1 | a0002c0002t0014g0124 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.703-3781A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988075 | ||||||
| chr12:30988141
|
A | G | 3 | a0001c0001t0004g0006a0001c0001t0014g0369a0001c0001t0014g0387 | 3 | HG02896.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.703-3715A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988141 | ||||||
| chr12:30988210
|
C | A | 3 | a0002c0002t0005g0130a0002c0002t0005g0131a0002c0002t0005g0143 | 3 | NA18953.hp1 NA18977.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.703-3646C>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988210 | ||||||
| chr12:30988212
|
A | C | 1 | a0001c0001t0005g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.703-3644A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988212 | ||||||
| chr12:30988270
|
T | C | 67 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(64): Show | 67 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.703-3586T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988270 | ||||||
| chr12:30988278
|
T | C | 255 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(252): Show | 256 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.703-3578T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988278 | ||||||
| chr12:30988339
|
C | G | 1 | a0001c0001t0014g0369 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.703-3517C>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988339 | ||||||
| chr12:30988461
|
C | T | 39 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(36): Show | 39 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.703-3395C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988461 | ||||||
| chr12:30988513
|
C | T | 5 | a0001c0001t0008g0063a0001c0001t0008g0067a0001c0001t0008g0089others(2): Show | 5 | NA18947.hp2 NA18954.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.703-3343C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988513 | ||||||
| chr12:30988573
|
A | G | 370 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(367): Show | 373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.703-3283A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988573 | ||||||
| chr12:30988605
|
A | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0235 | 2 | NA18945.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.703-3251A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988605 | ||||||
| chr12:30988724
|
C | T | 1 | a0001c0001t0042g0333 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.703-3132C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988724 | ||||||
| chr12:30988727
|
G | C | 187 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0099others(184): Show | 188 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.703-3129G>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30988727 | ||||||
| chr12:30989014
|
C | T | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.703-2842C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989014 | ||||||
| chr12:30989078
|
C | T | 14 | a0001c0001t0002g0376a0001c0001t0005g0104a0001c0001t0005g0118others(11): Show | 14 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.703-2778C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989078 | ||||||
| chr12:30989112
|
A | C | 85 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(82): Show | 85 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.703-2744A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989112 | ||||||
| chr12:30989328
|
T | A | 1 | a0001c0001t0002g0363 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.703-2528T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989328 | ||||||
| chr12:30989370
|
G | A | 14 | a0001c0001t0002g0376a0001c0001t0005g0104a0001c0001t0005g0118others(11): Show | 14 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.703-2486G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989370 | ||||||
| chr12:30989390
|
C | T | 19 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(16): Show | 19 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(16): Show |
intron_variant | MODIFIER | c.703-2466C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989390 | ||||||
| chr12:30989440
|
G | A | 2 | a0001c0001t0037g0014a0010c0012t0050g0248 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.703-2416G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989440 | ||||||
| chr12:30989680
|
A | G | 259 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(256): Show | 260 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.703-2176A>G | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989680 | ||||||
| chr12:30989840
|
G | A | 2 | a0001c0001t0037g0014a0010c0012t0050g0248 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.703-2016G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989840 | ||||||
| chr12:30989915
|
G | A | 50 | a0002c0002t0001g0031a0002c0002t0001g0035a0002c0002t0001g0036others(47): Show | 50 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.703-1941G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30989915 | ||||||
| chr12:30990008
|
C | T | 1 | a0001c0001t0014g0387 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.703-1848C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990008 | ||||||
| chr12:30990031
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.703-1825G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990031 | ||||||
| chr12:30990137
|
C | CGT | 23 | a0001c0001t0002g0363a0001c0001t0015g0366a0001c0001t0015g0367others(20): Show | 23 | HG01167.hp1 HG01192.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-1705_703-1704d others(4): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30990137 | |||||
| chr12:30990137
|
C | CGTGT | 69 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0056others(66): Show | 69 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.703-1707_703-1704d others(6): Show |
TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 30990137 | |||||
| chr12:30990137
|
C | T | 12 | a0001c0001t0002g0376a0001c0001t0005g0104a0001c0001t0005g0118others(9): Show | 12 | HG01257.hp2 HG01258.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.703-1719C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990137 | ||||||
| chr12:30990315
|
G | A | 2 | a0001c0001t0002g0274a0001c0001t0004g0006 | 2 | HG00639.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.703-1541G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990315 | ||||||
| chr12:30990327
|
C | T | 1 | a0001c0001t0010g0273 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.703-1529C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990327 | ||||||
| chr12:30990328
|
G | A | 1 | a0003c0003t0010g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.703-1528G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990328 | ||||||
| chr12:30990359
|
G | A | 1 | a0010c0012t0050g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703-1497G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990359 | ||||||
| chr12:30990369
|
C | T | 2 | a0002c0002t0001g0062a0002c0002t0001g0236 | 2 | NA18998.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.703-1487C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990369 | ||||||
| chr12:30990450
|
A | C | 381 | a0001c0001t0001g0020a0001c0001t0001g0042a0001c0001t0001g0043others(378): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.703-1406A>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990450 | ||||||
| chr12:30990698
|
C | T | 36 | a0002c0002t0001g0031a0002c0002t0001g0035a0002c0002t0001g0036others(33): Show | 36 | HG00423.hp2 HG00609.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.703-1158C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990698 | ||||||
| chr12:30990816
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.703-1040T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990816 | ||||||
| chr12:30990878
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.703-978C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30990878 | ||||||
| chr12:30991239
|
T | A | 1 | a0010c0012t0050g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703-617T>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30991239 | ||||||
| chr12:30991442
|
C | T | 1 | a0001c0001t0022g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.703-414C>T | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30991442 | ||||||
| chr12:30991586
|
T | C | 2 | a0001c0001t0029g0192a0001c0001t0029g0193 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.703-270T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30991586 | ||||||
| chr12:30991602
|
T | C | 48 | a0001c0001t0003g0041a0001c0001t0003g0074a0001c0001t0003g0083others(45): Show | 48 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.703-254T>C | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30991602 | ||||||
| chr12:30991698
|
G | A | 2 | a0001c0001t0025g0205a0001c0001t0025g0219 | 2 | HG01123.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.703-158G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30991698 | ||||||
| chr12:30991800
|
G | A | 19 | a0001c0001t0005g0301a0001c0001t0010g0029a0001c0001t0010g0050others(16): Show | 19 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.703-56G>A | TSPAN11 | ENSG00000110900.16 | transcript | ENST00000546076.6 | protein_coding | 7/7 | chr12 | 30991800 |