Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9169 |
|---|---|
| ensemblid | ENSG00000139218.18 |
| hgncid | 10784 |
| symbol | SCAF11 |
| name | SR-related CTD associated factor 11 |
| refseq_nuc | NM_004719.3 |
| refseq_prot | NP_004710.2 |
| ensembl_nuc | ENST00000369367.8 |
| ensembl_prot | ENSP00000358374.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 45919131 |
| end | 45990574 |
| strand | - |
| ver | v1.2 |
| region | chr12:45919131-45990574 |
| region5000 | chr12:45914131-45995574 |
| regionname0 | SCAF11_chr12_45919131_45990574 |
| regionname5000 | SCAF11_chr12_45914131_45995574 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1463 | 203 | 59 | 49 | 70 | 6 | 17 | 56 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002 | 0/0 | 1463 | 103 | 9 | 14 | 66 | 6 | 8 | 46 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0003 | 0/0 | 1463 | 10 | 5 | 0 | 0 | 0 | 5 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0004 | 0/0 | 1463 | 5 | 0 | 2 | 0 | 0 | 3 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0005 | 0/0 | 1463 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0006 | 0/0 | 1463 | 3 | 0 | 0 | 1 | 0 | 2 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0007 | 0/0 | 1463 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0008 | 0/0 | 1463 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0009 | 0/0 | 1463 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0010 | 0/0 | 1463 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0011 | 0/0 | 1463 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0012 | 0/0 | 1463 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0013 | 0/0 | 1463 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0014 | 0/0 | 1463 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0015 | 0/0 | 1463 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0016 | 0/0 | 1463 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0017 | 0/0 | 1463 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0018 | 0/0 | 1463 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0019 | 0/0 | 1463 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4392 | 157 | 23 | 45 | 66 | 6 | 15 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0002 | 0/0 | 4392 | 67 | 6 | 9 | 44 | 4 | 4 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0003 | 0/0 | 4392 | 30 | 2 | 5 | 17 | 2 | 4 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0004 | 0/0 | 4392 | 28 | 27 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0005 | 0/0 | 4392 | 10 | 5 | 0 | 0 | 0 | 5 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0006 | 0/0 | 4392 | 7 | 2 | 1 | 3 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0007 | 0/0 | 4392 | 6 | 4 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0008 | 0/0 | 4392 | 5 | 0 | 2 | 0 | 0 | 3 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0009 | 0/0 | 4392 | 4 | 0 | 0 | 4 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0010 | 0/0 | 4392 | 3 | 0 | 0 | 3 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0011 | 0/0 | 4392 | 3 | 0 | 0 | 1 | 0 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0012 | 0/0 | 4392 | 2 | 0 | 0 | 0 | 0 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0013 | 0/0 | 4392 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0014 | 0/0 | 4392 | 2 | 1 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0015 | 0/0 | 4392 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0016 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0017 | 0/0 | 4392 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0018 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0019 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0020 | 0/0 | 4392 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0021 | 0/0 | 4392 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0022 | 0/0 | 4392 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0023 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0024 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0025 | 0/0 | 4392 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0026 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0027 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0028 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0029 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0030 | 0/0 | 4392 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| c0031 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| 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 | 0/1 | 3161 | 110 | 17 | 24 | 50 | 3 | 15 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0002 | 0/0 | 3161 | 102 | 6 | 13 | 63 | 5 | 15 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0003 | 0/0 | 3161 | 94 | 45 | 24 | 20 | 3 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0004 | 0/0 | 3161 | 5 | 0 | 0 | 0 | 0 | 5 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0005 | 0/0 | 3161 | 5 | 0 | 2 | 0 | 0 | 3 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0006 | 0/0 | 3161 | 5 | 5 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0007 | 0/0 | 3161 | 5 | 0 | 0 | 5 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0008 | 0/0 | 3161 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0009 | 0/0 | 3161 | 2 | 1 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0010 | 0/0 | 3161 | 2 | 1 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0011 | 0/0 | 3161 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0012 | 0/0 | 3161 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0013 | 0/0 | 3161 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0014 | 0/0 | 3161 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0015 | 0/0 | 3161 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0016 | 0/0 | 3161 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0017 | 0/0 | 3161 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0018 | 0/0 | 3161 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0019 | 1/0 | 3161 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0020 | 0/0 | 3161 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0021 | 0/0 | 3161 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| t0022 | 0/0 | 3161 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0005 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4392 | 157 | 23 | 45 | 66 | 6 | 15 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0004 | 0/0 | 4392 | 28 | 27 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0006 | 0/0 | 4392 | 7 | 2 | 1 | 3 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0007 | 0/0 | 4392 | 6 | 4 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0015 | 0/0 | 4392 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0023 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0025 | 0/0 | 4392 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0029 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0002 | 0/0 | 4392 | 67 | 6 | 9 | 44 | 4 | 4 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0003 | 0/0 | 4392 | 30 | 2 | 5 | 17 | 2 | 4 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0010 | 0/0 | 4392 | 3 | 0 | 0 | 3 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0018 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0019 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0031 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0003c0005 | 0/0 | 4392 | 10 | 5 | 0 | 0 | 0 | 5 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0004c0008 | 0/0 | 4392 | 5 | 0 | 2 | 0 | 0 | 3 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0005c0009 | 0/0 | 4392 | 4 | 0 | 0 | 4 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0006c0011 | 0/0 | 4392 | 3 | 0 | 0 | 1 | 0 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0007c0012 | 0/0 | 4392 | 2 | 0 | 0 | 0 | 0 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0008c0013 | 0/0 | 4392 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0009c0014 | 0/0 | 4392 | 2 | 1 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0010c0028 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0011c0027 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0012c0017 | 0/0 | 4392 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0013c0030 | 0/0 | 4392 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0014c0022 | 0/0 | 4392 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0015c0024 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0016c0026 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0017c0020 | 0/0 | 4392 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0018c0021 | 0/0 | 4392 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0019c0016 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7552 | 92 | 10 | 22 | 43 | 3 | 13 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0001t0003 | 0/0 | 7552 | 56 | 11 | 20 | 20 | 3 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0001t0010 | 0/0 | 7552 | 2 | 1 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0001t0011 | 0/0 | 7552 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0001t0012 | 0/0 | 7552 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0001t0013 | 0/0 | 7552 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0001t0014 | 0/0 | 7552 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0001t0019 | 1/0 | 7552 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0001t0020 | 0/0 | 7552 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0001t0021 | 0/0 | 7552 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0004t0003 | 0/0 | 7552 | 26 | 26 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0004t0009 | 0/0 | 7552 | 2 | 1 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0006t0001 | 0/0 | 7552 | 7 | 2 | 1 | 3 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0007t0003 | 0/0 | 7552 | 4 | 2 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0007t0008 | 0/0 | 7552 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0015t0001 | 0/0 | 7552 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0023t0015 | 0/0 | 7552 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0025t0001 | 0/0 | 7552 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0001c0029t0003 | 0/0 | 7552 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0002t0002 | 0/0 | 7552 | 63 | 4 | 9 | 43 | 3 | 4 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0002t0003 | 0/0 | 7552 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0002t0016 | 0/0 | 7552 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0002t0017 | 0/0 | 7552 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0003t0002 | 0/0 | 7552 | 24 | 2 | 4 | 12 | 2 | 4 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0003t0007 | 0/0 | 7552 | 5 | 0 | 0 | 5 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0003t0018 | 0/0 | 7552 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0010t0002 | 0/0 | 7552 | 3 | 0 | 0 | 3 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0018t0002 | 0/0 | 7552 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0019t0003 | 0/0 | 7552 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0002c0031t0002 | 0/0 | 7552 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0003c0005t0004 | 0/0 | 7552 | 5 | 0 | 0 | 0 | 0 | 5 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0003c0005t0006 | 0/0 | 7552 | 5 | 5 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0004c0008t0005 | 0/0 | 7552 | 5 | 0 | 2 | 0 | 0 | 3 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0005c0009t0001 | 0/0 | 7552 | 4 | 0 | 0 | 4 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0006c0011t0002 | 0/0 | 7552 | 3 | 0 | 0 | 1 | 0 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0007c0012t0002 | 0/0 | 7552 | 2 | 0 | 0 | 0 | 0 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0008c0013t0001 | 0/0 | 7552 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0009c0014t0003 | 0/0 | 7552 | 2 | 1 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0010c0028t0002 | 0/0 | 7552 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0011c0027t0022 | 0/0 | 7552 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0012c0017t0002 | 0/0 | 7552 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0013c0030t0003 | 0/0 | 7552 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0014c0022t0001 | 0/0 | 7552 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0015c0024t0001 | 0/0 | 7552 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0016c0026t0003 | 0/0 | 7552 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0017c0020t0002 | 0/0 | 7552 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0018c0021t0002 | 0/0 | 7552 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| a0019c0016t0002 | 0/0 | 7552 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | copy fasta | chr12 | 45914131 | 45995574 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0010g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0010g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0011g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0012g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0013g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0014g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0019g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0020g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0001t0021g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0009g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0004t0009g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0006t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0006t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0006t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0006t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0006t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0006t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0006t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0007t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0007t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0007t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0007t0008g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0007t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0015t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0015t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0023t0015g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0025t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0001c0029t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0016g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0002t0017g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0007g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0003t0018g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0010t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0010t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0010t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0018t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0019t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0002c0031t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0003c0005t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0003c0005t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0003c0005t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0003c0005t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0003c0005t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0003c0005t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0003c0005t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0003c0005t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0003c0005t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0003c0005t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0004c0008t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0004c0008t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0004c0008t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0004c0008t0005g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0004c0008t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0005c0009t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0005c0009t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0005c0009t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0005c0009t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0006c0011t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0006c0011t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0007c0012t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0007c0012t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0008c0013t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0008c0013t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0009c0014t0003g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0010c0028t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0011c0027t0022g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0012c0017t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0013c0030t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0014c0022t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0015c0024t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0016c0026t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0017c0020t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0018c0021t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| a0019c0016t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0081 | EUR | GBR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0174 | EUR | GBR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0176 | EUR | GBR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00140 | hp2 | a0002 | c0003 | t0002 | g0098 | EUR | GBR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | FIN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0038 | EUR | FIN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00408 | hp2 | a0002 | c0003 | t0002 | g0100 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00544 | hp2 | a0002 | c0003 | t0002 | g0093 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00609 | hp1 | a0002 | c0031 | t0002 | g0086 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0303 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00738 | hp2 | a0013 | c0030 | t0003 | g0196 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01069 | hp1 | a0001 | c0001 | t0011 | g0261 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01071 | hp1 | a0004 | c0008 | t0005 | g0046 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0052 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0185 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01106 | hp1 | a0002 | c0003 | t0018 | g0037 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01109 | hp1 | a0009 | c0014 | t0003 | g0024 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01167 | hp1 | a0001 | c0006 | t0001 | g0264 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01167 | hp2 | a0001 | c0007 | t0003 | g0022 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01169 | hp1 | a0001 | c0007 | t0003 | g0022 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0051 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01175 | hp2 | a0001 | c0004 | t0009 | g0283 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0113 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01192 | hp2 | a0014 | c0022 | t0001 | g0205 | AMR | PUR | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01256 | hp1 | a0002 | c0003 | t0002 | g0096 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01257 | hp2 | a0002 | c0003 | t0002 | g0012 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01258 | hp2 | a0002 | c0003 | t0002 | g0012 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01346 | hp1 | a0001 | c0001 | t0010 | g0310 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01358 | hp2 | a0004 | c0008 | t0005 | g0070 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01433 | hp2 | a0001 | c0001 | t0020 | g0189 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01515 | hp1 | a0002 | c0002 | t0017 | g0072 | EUR | IBS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01884 | hp1 | a0002 | c0002 | t0003 | g0276 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01884 | hp2 | a0001 | c0004 | t0003 | g0279 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0302 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0042 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02040 | hp1 | a0002 | c0003 | t0002 | g0101 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02071 | hp1 | a0010 | c0028 | t0002 | g0041 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02074 | hp1 | a0002 | c0003 | t0002 | g0110 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02083 | hp2 | a0002 | c0003 | t0002 | g0104 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02132 | hp2 | a0002 | c0003 | t0002 | g0108 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0078 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02155 | hp1 | a0002 | c0002 | t0016 | g0047 | EAS | CDX | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | CDX | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | CDX | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | CDX | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02257 | hp1 | a0001 | c0004 | t0003 | g0286 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02257 | hp2 | a0002 | c0019 | t0003 | g0296 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02258 | hp1 | a0009 | c0014 | t0003 | g0024 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02280 | hp1 | a0001 | c0004 | t0003 | g0284 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02280 | hp2 | a0002 | c0003 | t0002 | g0097 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0083 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PEL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02451 | hp1 | a0001 | c0004 | t0003 | g0021 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02451 | hp2 | a0003 | c0005 | t0006 | g0134 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02602 | hp1 | a0004 | c0008 | t0005 | g0069 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02602 | hp2 | a0001 | c0006 | t0001 | g0252 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0292 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02615 | hp2 | a0001 | c0004 | t0003 | g0020 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02622 | hp1 | a0015 | c0024 | t0001 | g0132 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02622 | hp2 | a0001 | c0004 | t0003 | g0278 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02630 | hp1 | a0001 | c0004 | t0003 | g0271 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02647 | hp1 | a0003 | c0005 | t0006 | g0135 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02647 | hp2 | a0001 | c0004 | t0003 | g0295 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02683 | hp1 | a0007 | c0012 | t0002 | g0066 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02698 | hp2 | a0004 | c0008 | t0005 | g0056 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0061 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02717 | hp2 | a0001 | c0015 | t0001 | g0250 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02735 | hp1 | a0002 | c0003 | t0002 | g0036 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02735 | hp2 | a0017 | c0020 | t0002 | g0035 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0043 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02738 | hp2 | a0003 | c0005 | t0004 | g0028 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0309 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02886 | hp1 | a0001 | c0004 | t0003 | g0002 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02886 | hp2 | a0003 | c0005 | t0006 | g0136 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02895 | hp1 | a0001 | c0004 | t0003 | g0287 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02895 | hp2 | a0008 | c0013 | t0001 | g0225 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0291 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02896 | hp2 | a0001 | c0006 | t0001 | g0223 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0290 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02897 | hp2 | a0008 | c0013 | t0001 | g0226 | AFR | GWD | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02922 | hp1 | a0001 | c0004 | t0003 | g0129 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02922 | hp2 | a0001 | c0004 | t0003 | g0277 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0305 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02965 | hp2 | a0003 | c0005 | t0006 | g0137 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02970 | hp1 | a0001 | c0004 | t0003 | g0273 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02976 | hp1 | a0001 | c0006 | t0001 | g0222 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02976 | hp2 | a0001 | c0004 | t0003 | g0285 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03017 | hp2 | a0007 | c0012 | t0002 | g0074 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03098 | hp1 | a0003 | c0005 | t0006 | g0138 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03098 | hp2 | a0001 | c0007 | t0008 | g0307 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03130 | hp2 | a0001 | c0004 | t0003 | g0272 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03195 | hp1 | a0001 | c0004 | t0003 | g0002 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03209 | hp1 | a0001 | c0004 | t0003 | g0289 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03209 | hp2 | a0016 | c0026 | t0003 | g0275 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03225 | hp1 | a0001 | c0007 | t0008 | g0306 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03225 | hp2 | a0001 | c0004 | t0003 | g0270 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03239 | hp1 | a0012 | c0017 | t0002 | g0109 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03239 | hp2 | a0003 | c0005 | t0004 | g0026 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03453 | hp1 | a0001 | c0004 | t0003 | g0133 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03453 | hp2 | a0001 | c0007 | t0003 | g0293 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03486 | hp1 | a0001 | c0004 | t0009 | g0282 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03490 | hp1 | a0002 | c0003 | t0002 | g0013 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03492 | hp1 | a0018 | c0021 | t0002 | g0044 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03492 | hp2 | a0002 | c0003 | t0002 | g0013 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03516 | hp2 | a0001 | c0015 | t0001 | g0249 | AFR | ESN | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03579 | hp1 | a0001 | c0004 | t0003 | g0280 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03579 | hp2 | a0001 | c0004 | t0003 | g0288 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0300 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03704 | hp1 | a0003 | c0005 | t0004 | g0029 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0121 | SAS | BEB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03927 | hp2 | a0002 | c0003 | t0002 | g0102 | SAS | BEB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03942 | hp1 | a0004 | c0008 | t0005 | g0065 | SAS | BEB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG04184 | hp1 | a0006 | c0011 | t0002 | g0008 | SAS | BEB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0118 | SAS | STU | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG04199 | hp2 | a0001 | c0025 | t0001 | g0209 | SAS | STU | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG04204 | hp2 | a0003 | c0005 | t0004 | g0027 | SAS | STU | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0117 | SAS | STU | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18612 | hp1 | a0005 | c0009 | t0001 | g0149 | EAS | CHB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | CHB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | CHB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18945 | hp2 | a0002 | c0003 | t0002 | g0106 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18947 | hp2 | a0002 | c0010 | t0002 | g0116 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18950 | hp2 | a0002 | c0003 | t0007 | g0091 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18951 | hp2 | a0001 | c0006 | t0001 | g0241 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18960 | hp2 | a0002 | c0003 | t0007 | g0103 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18967 | hp1 | a0005 | c0009 | t0001 | g0148 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18969 | hp1 | a0001 | c0006 | t0001 | g0243 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18970 | hp1 | a0002 | c0010 | t0002 | g0115 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18972 | hp2 | a0019 | c0016 | t0002 | g0111 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18973 | hp1 | a0002 | c0003 | t0002 | g0090 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18974 | hp1 | a0011 | c0027 | t0022 | g0311 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18977 | hp1 | a0002 | c0003 | t0002 | g0099 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18979 | hp1 | a0001 | c0001 | t0014 | g0168 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18980 | hp2 | a0002 | c0003 | t0007 | g0040 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18983 | hp1 | a0005 | c0009 | t0001 | g0147 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18984 | hp2 | a0002 | c0003 | t0002 | g0092 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18993 | hp1 | a0002 | c0003 | t0007 | g0105 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA18993 | hp2 | a0001 | c0023 | t0015 | g0139 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19000 | hp2 | a0002 | c0003 | t0002 | g0125 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19001 | hp2 | a0002 | c0018 | t0002 | g0039 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19030 | hp1 | a0001 | c0004 | t0003 | g0281 | AFR | LWK | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19062 | hp1 | a0001 | c0001 | t0012 | g0304 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19065 | hp2 | a0002 | c0003 | t0007 | g0089 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19070 | hp2 | a0001 | c0006 | t0001 | g0242 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19074 | hp2 | a0001 | c0001 | t0021 | g0312 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19077 | hp1 | a0006 | c0011 | t0002 | g0112 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19078 | hp1 | a0002 | c0010 | t0002 | g0127 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19085 | hp1 | a0002 | c0003 | t0002 | g0094 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA19091 | hp2 | a0005 | c0009 | t0001 | g0167 | EAS | JPT | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0114 | EUR | TSI | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | TSI | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA20805 | hp1 | a0002 | c0003 | t0002 | g0107 | EUR | TSI | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0191 | EUR | TSI | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA20905 | hp1 | a0006 | c0011 | t0002 | g0008 | SAS | GIH | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA20905 | hp2 | a0003 | c0005 | t0004 | g0025 | SAS | GIH | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0053 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG01123 | hp2 | a0002 | c0003 | t0002 | g0126 | AMR | CLM | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0049 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02109 | hp2 | a0001 | c0004 | t0003 | g0002 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02486 | hp1 | a0001 | c0004 | t0003 | g0021 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0119 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02559 | hp1 | a0002 | c0002 | t0003 | g0128 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG02559 | hp2 | a0001 | c0007 | t0003 | g0294 | AFR | ACB | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG03471 | hp2 | a0001 | c0004 | t0003 | g0002 | AFR | MSL | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | USA | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| HG06807 | hp2 | a0001 | c0004 | t0003 | g0020 | AFR | USA | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA20300 | hp1 | a0002 | c0003 | t0002 | g0095 | AFR | USA | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | USA | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA21309 | hp1 | a0001 | c0029 | t0003 | g0130 | AFR | LWK | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | LWK | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0214 | REF | REF | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0019 | g0199 | REF | REF | SCAF11_chr12_45914131_45995574 | SCAF11 | chr12 | 45914131 | 45995574 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45923079
|
T | C | 1 | a0009 | 2 | HG01109.hp1 HG02258.hp1 |
missense_variant | MODERATE | c.3982A>G | p.Asn1328Asp | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 13/15 | 4225/7552 | 3982/4392 | 1328/1463 | chr12 | 45923079 | ||
| chr12:45924829
|
G | A | 1 | a0015 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.3805C>T | p.Pro1269Ser | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/15 | 4048/7552 | 3805/4392 | 1269/1463 | chr12 | 45924829 | ||
| chr12:45924853
|
C | G | 1 | a0005 | 4 | NA18612.hp1 NA18967.hp1 NA18983.hp1 others(1): Show |
missense_variant | MODERATE | c.3781G>C | p.Val1261Leu | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/15 | 4024/7552 | 3781/4392 | 1261/1463 | chr12 | 45924853 | ||
| chr12:45926528
|
G | T | 1 | a0008 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.3173C>A | p.Ser1058Tyr | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 3416/7552 | 3173/4392 | 1058/1463 | chr12 | 45926528 | ||
| chr12:45926773
|
T | A | 1 | a0017 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.2928A>T | p.Arg976Ser | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 3171/7552 | 2928/4392 | 976/1463 | chr12 | 45926773 | ||
| chr12:45926829
|
C | A | 1 | a0016 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.2872G>T | p.Asp958Tyr | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 3115/7552 | 2872/4392 | 958/1463 | chr12 | 45926829 | ||
| chr12:45927093
|
C | A | 1 | a0006 | 3 | HG04184.hp1 NA19077.hp1 NA20905.hp1 |
missense_variant | MODERATE | c.2608G>T | p.Asp870Tyr | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 2851/7552 | 2608/4392 | 870/1463 | chr12 | 45927093 | ||
| chr12:45927161
|
C | T | 1 | a0014 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.2540G>A | p.Arg847His | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 2783/7552 | 2540/4392 | 847/1463 | chr12 | 45927161 | ||
| chr12:45927341
|
G | C | 1 | a0009 | 2 | HG01109.hp1 HG02258.hp1 |
missense_variant | MODERATE | c.2360C>G | p.Pro787Arg | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 2603/7552 | 2360/4392 | 787/1463 | chr12 | 45927341 | ||
| chr12:45927448
|
G | C | 1 | a0018 | 1 | HG03492.hp1 | missense_variant | MODERATE | c.2253C>G | p.His751Gln | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 2496/7552 | 2253/4392 | 751/1463 | chr12 | 45927448 | ||
| chr12:45927658
|
T | G | 1 | a0013 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.2043A>C | p.Leu681Phe | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 2286/7552 | 2043/4392 | 681/1463 | chr12 | 45927658 | ||
| chr12:45927731
|
A | T | 9 | a0002a0004a0006others(6): Show | 118 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
missense_variant | MODERATE | c.1970T>A | p.Phe657Tyr | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 2213/7552 | 1970/4392 | 657/1463 | chr12 | 45927731 | ||
| chr12:45927872
|
T | C | 1 | a0019 | 1 | NA18972.hp2 | missense_variant | MODERATE | c.1829A>G | p.Lys610Arg | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 2072/7552 | 1829/4392 | 610/1463 | chr12 | 45927872 | ||
| chr12:45927949
|
T | C | 1 | a0003 | 10 | HG02451.hp2 HG02647.hp1 HG02738.hp2 others(7): Show |
missense_variant | MODERATE | c.1752A>G | p.Ile584Met | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 1995/7552 | 1752/4392 | 584/1463 | chr12 | 45927949 | ||
| chr12:45928007
|
G | A | 1 | a0012 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.1694C>T | p.Ser565Phe | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 1937/7552 | 1694/4392 | 565/1463 | chr12 | 45928007 | ||
| chr12:45928584
|
T | G | 1 | a0011 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1117A>C | p.Lys373Gln | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 1360/7552 | 1117/4392 | 373/1463 | chr12 | 45928584 | ||
| chr12:45928653
|
C | T | 1 | a0004 | 5 | HG01071.hp1 HG01358.hp2 HG02602.hp1 others(2): Show |
missense_variant | MODERATE | c.1048G>A | p.Gly350Ser | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 1291/7552 | 1048/4392 | 350/1463 | chr12 | 45928653 | ||
| chr12:45928685
|
G | A | 1 | a0011 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1016C>T | p.Pro339Leu | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 1259/7552 | 1016/4392 | 339/1463 | chr12 | 45928685 | ||
| chr12:45931530
|
T | G | 1 | a0010 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.817A>C | p.Ser273Arg | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/15 | 1060/7552 | 817/4392 | 273/1463 | chr12 | 45931530 | ||
| chr12:45945300
|
C | T | 1 | a0007 | 2 | HG02683.hp1 HG03017.hp2 |
missense_variant | MODERATE | c.412G>A | p.Val138Ile | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/15 | 655/7552 | 412/4392 | 138/1463 | chr12 | 45945300 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45922543
|
A | G | 1 | a0001c0023 | 1 | NA18993.hp2 | synonymous_variant | LOW | c.4165T>C | p.Leu1389Leu | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 14/15 | 4408/7552 | 4165/4392 | 1389/1463 | chr12 | 45922543 | ||
| chr12:45923032
|
T | G | 1 | a0002c0019 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.4029A>C | p.Ser1343Ser | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 13/15 | 4272/7552 | 4029/4392 | 1343/1463 | chr12 | 45923032 | ||
| chr12:45924983
|
T | C | 1 | a0001c0025 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.3651A>G | p.Gln1217Gln | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/15 | 3894/7552 | 3651/4392 | 1217/1463 | chr12 | 45924983 | ||
| chr12:45926638
|
G | A | 3 | a0001c0006a0001c0025a0015c0024 | 9 | HG01167.hp1 HG02602.hp2 HG02622.hp1 others(6): Show |
synonymous_variant | LOW | c.3063C>T | p.Pro1021Pro | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 3306/7552 | 3063/4392 | 1021/1463 | chr12 | 45926638 | ||
| chr12:45926686
|
T | C | 1 | a0002c0010 | 3 | NA18947.hp2 NA18970.hp1 NA19078.hp1 |
synonymous_variant | LOW | c.3015A>G | p.Leu1005Leu | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 3258/7552 | 3015/4392 | 1005/1463 | chr12 | 45926686 | ||
| chr12:45927634
|
G | A | 1 | a0001c0004 | 28 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(25): Show |
synonymous_variant | LOW | c.2067C>T | p.Thr689Thr | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 2310/7552 | 2067/4392 | 689/1463 | chr12 | 45927634 | ||
| chr12:45927919
|
T | C | 1 | a0001c0015 | 2 | HG02717.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.1782A>G | p.Glu594Glu | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 2025/7552 | 1782/4392 | 594/1463 | chr12 | 45927919 | ||
| chr12:45928462
|
A | T | 1 | a0002c0018 | 1 | NA19001.hp2 | synonymous_variant | LOW | c.1239T>A | p.Ser413Ser | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 1482/7552 | 1239/4392 | 413/1463 | chr12 | 45928462 | ||
| chr12:45928666
|
C | T | 4 | a0002c0003a0010c0028a0012c0017others(1): Show | 33 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(30): Show |
synonymous_variant | LOW | c.1035G>A | p.Gly345Gly | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/15 | 1278/7552 | 1035/4392 | 345/1463 | chr12 | 45928666 | ||
| chr12:45945250
|
A | G | 1 | a0001c0007 | 6 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.462T>C | p.His154His | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/15 | 705/7552 | 462/4392 | 154/1463 | chr12 | 45945250 | ||
| chr12:45948508
|
T | C | 2 | a0001c0029a0013c0030 | 2 | HG00738.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.327A>G | p.Thr109Thr | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/15 | 570/7552 | 327/4392 | 109/1463 | chr12 | 45948508 | ||
| chr12:45961847
|
G | A | 1 | a0002c0031 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.72C>T | p.Asn24Asn | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/15 | 315/7552 | 72/4392 | 24/1463 | chr12 | 45961847 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45919272
|
A | G | 1 | a0001c0001t0014 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2776T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 2776 | chr12 | 45919272 | |||||
| chr12:45919404
|
C | G | 1 | a0002c0002t0017 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2644G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 2644 | chr12 | 45919404 | |||||
| chr12:45919643
|
C | T | 1 | a0002c0003t0018 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2405G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 2405 | chr12 | 45919643 | |||||
| chr12:45919855
|
G | A | 17 | a0002c0002t0002a0002c0002t0016a0002c0002t0017others(14): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2193C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 2193 | chr12 | 45919855 | |||||
| chr12:45919998
|
A | C | 1 | a0002c0002t0016 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2050T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 2050 | chr12 | 45919998 | |||||
| chr12:45920037
|
T | C | 1 | a0003c0005t0006 | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2011A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 2011 | chr12 | 45920037 | |||||
| chr12:45920243
|
T | C | 1 | a0002c0003t0018 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1805A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 1805 | chr12 | 45920243 | |||||
| chr12:45920327
|
C | G | 1 | a0001c0001t0013 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1721G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 1721 | chr12 | 45920327 | |||||
| chr12:45920335
|
T | C | 1 | a0001c0023t0015 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1713A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 1713 | chr12 | 45920335 | |||||
| chr12:45920609
|
A | G | 14 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(11): Show | 116 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1439T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 1439 | chr12 | 45920609 | |||||
| chr12:45920673
|
C | A | 1 | a0001c0004t0009 | 2 | HG01175.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1375G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 1375 | chr12 | 45920673 | |||||
| chr12:45920673
|
C | T | 1 | a0001c0001t0012 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1375G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 1375 | chr12 | 45920673 | |||||
| chr12:45920705
|
T | C | 1 | a0004c0008t0005 | 5 | HG01071.hp1 HG01358.hp2 HG02602.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1343A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 1343 | chr12 | 45920705 | |||||
| chr12:45920729
|
G | A | 1 | a0001c0007t0008 | 2 | HG03098.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1319C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 1319 | chr12 | 45920729 | |||||
| chr12:45920895
|
A | G | 1 | a0001c0007t0008 | 2 | HG03098.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1153T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 1153 | chr12 | 45920895 | |||||
| chr12:45920931
|
C | T | 1 | a0001c0001t0011 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1117G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 1117 | chr12 | 45920931 | |||||
| chr12:45921543
|
T | G | 1 | a0003c0005t0006 | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*505A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 505 | chr12 | 45921543 | |||||
| chr12:45921627
|
G | A | 1 | a0002c0003t0007 | 5 | NA18950.hp2 NA18960.hp2 NA18980.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*421C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 421 | chr12 | 45921627 | |||||
| chr12:45921655
|
C | T | 47 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(44): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
3_prime_UTR_variant | MODIFIER | c.*393G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 393 | chr12 | 45921655 | |||||
| chr12:45922028
|
C | A | 1 | a0001c0001t0020 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*20G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 15/15 | 20 | chr12 | 45922028 | |||||
| chr12:45990517
|
G | A | 1 | a0001c0001t0010 | 2 | HG01346.hp1 HG02809.hp1 |
5_prime_UTR_variant | MODIFIER | c.-186C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/15 | 26350 | chr12 | 45990517 | |||||
| chr12:45990523
|
C | A | 2 | a0001c0001t0021a0011c0027t0022 | 2 | NA18974.hp1 NA19074.hp2 |
5_prime_UTR_variant | MODIFIER | c.-192G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/15 | 26356 | chr12 | 45990523 | |||||
| chr12:45990565
|
A | G | 1 | a0003c0005t0004 | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-234T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/15 | 26398 | chr12 | 45990565 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45922735
|
T | C | 1 | a0001c0001t0003g0175 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4126-153A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 13/14 | chr12 | 45922735 | ||||||
| chr12:45923221
|
T | A | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 117 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.3907-67A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45923221 | ||||||
| chr12:45923245
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3907-91T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45923245 | ||||||
| chr12:45923337
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3907-183G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45923337 | ||||||
| chr12:45923649
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3907-495A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45923649 | ||||||
| chr12:45923759
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3907-605A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45923759 | ||||||
| chr12:45923761
|
C | T | 1 | a0001c0004t0003g0272 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3907-607G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45923761 | ||||||
| chr12:45923768
|
C | T | 2 | a0002c0002t0002g0009a0002c0002t0002g0068 | 3 | NA18944.hp1 NA18959.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.3907-614G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45923768 | ||||||
| chr12:45923806
|
C | T | 3 | a0001c0006t0001g0241a0001c0006t0001g0242a0001c0006t0001g0243 | 3 | NA18951.hp2 NA18969.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.3907-652G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45923806 | ||||||
| chr12:45923830
|
C | T | 1 | a0002c0002t0017g0072 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3907-676G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45923830 | ||||||
| chr12:45923838
|
C | T | 1 | a0001c0001t0003g0173 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3907-684G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45923838 | ||||||
| chr12:45924179
|
T | A | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3906+549A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45924179 | ||||||
| chr12:45924187
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3906+541T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45924187 | ||||||
| chr12:45924208
|
A | C | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3906+520T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45924208 | ||||||
| chr12:45924330
|
T | C | 1 | a0004c0008t0005g0070 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3906+398A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45924330 | ||||||
| chr12:45924335
|
G | C | 1 | a0002c0003t0002g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3906+393C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 12/14 | chr12 | 45924335 | ||||||
| chr12:45925171
|
A | G | 4 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0210others(1): Show | 4 | NA18966.hp2 NA19001.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.3560-97T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/14 | chr12 | 45925171 | ||||||
| chr12:45925359
|
C | G | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.3560-285G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/14 | chr12 | 45925359 | ||||||
| chr12:45925462
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3560-388A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/14 | chr12 | 45925462 | ||||||
| chr12:45925644
|
TA | T | 8 | a0001c0001t0001g0216a0001c0001t0001g0234a0001c0001t0003g0169others(5): Show | 8 | HG01891.hp2 HG02818.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3559+497delT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/14 | chr12 | 45925644 | ||||||
| chr12:45925731
|
C | T | 1 | a0002c0002t0002g0121 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3559+411G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 11/14 | chr12 | 45925731 | ||||||
| chr12:45928871
|
T | A | 2 | a0001c0004t0003g0280a0001c0025t0001g0209 | 2 | HG03579.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.842-12A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45928871 | ||||||
| chr12:45928871
|
TA | T | 8 | a0001c0001t0001g0151a0002c0002t0002g0062a0002c0002t0002g0077others(5): Show | 8 | HG02647.hp1 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.842-13delT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45928871 | ||||||
| chr12:45928872
|
A | T | 1 | a0002c0003t0018g0037 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.842-13T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45928872 | ||||||
| chr12:45928982
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.842-123T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45928982 | ||||||
| chr12:45929020
|
A | G | 1 | a0001c0001t0001g0019 | 2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.842-161T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45929020 | ||||||
| chr12:45929098
|
G | GA | 24 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(21): Show | 29 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.842-240dupT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45929098 | ||||||
| chr12:45929098
|
GA | G | 7 | a0001c0001t0001g0151a0001c0001t0003g0290a0001c0001t0003g0291others(4): Show | 8 | HG01109.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.842-240delT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45929098 | ||||||
| chr12:45929227
|
C | T | 1 | a0001c0001t0003g0190 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.842-368G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45929227 | ||||||
| chr12:45929760
|
T | C | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.842-901A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45929760 | ||||||
| chr12:45929928
|
T | G | 112 | a0001c0001t0003g0274a0001c0001t0010g0309a0001c0001t0010g0310others(109): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.842-1069A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45929928 | ||||||
| chr12:45929999
|
TA | T | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.842-1141delT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45929999 | ||||||
| chr12:45930222
|
T | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0166 | 2 | NA18950.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.841+1284A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45930222 | ||||||
| chr12:45930440
|
GTTTT | G | 3 | a0001c0004t0003g0277a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG01884.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.841+1062_841+1065d others(6): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45930440 | ||||||
| chr12:45930445
|
G | GT | 6 | a0001c0001t0001g0238a0001c0001t0003g0290a0001c0001t0003g0291others(3): Show | 6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.841+1060dupA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45930445 | ||||||
| chr12:45930445
|
G | T | 1 | a0002c0002t0003g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.841+1061C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45930445 | ||||||
| chr12:45930456
|
G | GT | 63 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(60): Show | 68 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.841+1049dupA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45930456 | ||||||
| chr12:45930456
|
G | T | 30 | a0001c0001t0001g0238a0001c0001t0001g0260a0001c0001t0003g0290others(27): Show | 36 | HG01109.hp1 HG01175.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.841+1050C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45930456 | ||||||
| chr12:45930554
|
C | T | 3 | a0001c0004t0003g0278a0001c0004t0003g0281a0001c0004t0003g0287 | 3 | HG02622.hp2 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.841+952G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45930554 | ||||||
| chr12:45930769
|
T | A | 1 | a0002c0019t0003g0296 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.841+737A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45930769 | ||||||
| chr12:45930808
|
T | C | 1 | a0001c0001t0003g0201 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.841+698A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45930808 | ||||||
| chr12:45930912
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.841+594G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 10/14 | chr12 | 45930912 | ||||||
| chr12:45931826
|
G | A | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-214C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 9/14 | chr12 | 45931826 | ||||||
| chr12:45932291
|
C | A | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-679G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 9/14 | chr12 | 45932291 | ||||||
| chr12:45932359
|
G | GT | 24 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(21): Show | 29 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.735-748dupA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 9/14 | chr12 | 45932359 | ||||||
| chr12:45932365
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0145others(13): Show | 19 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.735-753A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 9/14 | chr12 | 45932365 | ||||||
| chr12:45932499
|
T | C | 268 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(265): Show | 294 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.734+632A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 9/14 | chr12 | 45932499 | ||||||
| chr12:45932636
|
T | A | 310 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(307): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.734+495A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 9/14 | chr12 | 45932636 | ||||||
| chr12:45932793
|
G | T | 269 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(266): Show | 295 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.734+338C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 9/14 | chr12 | 45932793 | ||||||
| chr12:45932799
|
C | G | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.734+332G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 9/14 | chr12 | 45932799 | ||||||
| chr12:45932938
|
T | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0166 | 2 | NA18950.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.734+193A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 9/14 | chr12 | 45932938 | ||||||
| chr12:45933057
|
T | C | 3 | a0002c0002t0002g0038a0002c0002t0002g0042a0002c0002t0002g0043 | 3 | HG00280.hp2 HG01993.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.734+74A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 9/14 | chr12 | 45933057 | ||||||
| chr12:45933306
|
G | C | 7 | a0001c0001t0001g0224a0001c0001t0001g0228a0001c0001t0001g0248others(4): Show | 7 | HG00609.hp2 HG00673.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.633-74C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 8/14 | chr12 | 45933306 | ||||||
| chr12:45933450
|
T | C | 1 | a0002c0003t0002g0092 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.633-218A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 8/14 | chr12 | 45933450 | ||||||
| chr12:45933826
|
A | G | 2 | a0001c0015t0001g0249a0001c0015t0001g0250 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.632+350T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 8/14 | chr12 | 45933826 | ||||||
| chr12:45933958
|
T | G | 5 | a0001c0007t0003g0022a0001c0007t0003g0293a0001c0007t0003g0294others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.632+218A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 8/14 | chr12 | 45933958 | ||||||
| chr12:45934341
|
G | A | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.523-56C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 7/14 | chr12 | 45934341 | ||||||
| chr12:45934576
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.464-71C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45934576 | ||||||
| chr12:45934606
|
C | G | 1 | a0001c0001t0003g0023 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.464-101G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45934606 | ||||||
| chr12:45934765
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.464-260T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45934765 | ||||||
| chr12:45934872
|
C | T | 1 | a0001c0004t0009g0282 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.464-367G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45934872 | ||||||
| chr12:45934895
|
CA | C | 31 | a0002c0003t0002g0012a0002c0003t0002g0013a0002c0003t0002g0036others(28): Show | 33 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.464-391delT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45934895 | ||||||
| chr12:45934923
|
C | T | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-418G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45934923 | ||||||
| chr12:45934949
|
C | A | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-444G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45934949 | ||||||
| chr12:45935205
|
T | A | 2 | a0001c0015t0001g0249a0001c0015t0001g0250 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.464-700A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45935205 | ||||||
| chr12:45935334
|
C | T | 3 | a0001c0007t0003g0022a0001c0007t0003g0293a0001c0007t0003g0294 | 4 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-829G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45935334 | ||||||
| chr12:45935392
|
A | C | 1 | a0001c0001t0001g0258 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.464-887T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45935392 | ||||||
| chr12:45935409
|
A | T | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 117 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.464-904T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45935409 | ||||||
| chr12:45935454
|
C | T | 1 | a0002c0002t0003g0276 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.464-949G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45935454 | ||||||
| chr12:45935466
|
A | C | 1 | a0002c0003t0002g0036 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.464-961T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45935466 | ||||||
| chr12:45935506
|
T | A | 2 | a0002c0003t0002g0094a0002c0003t0002g0099 | 2 | NA18977.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.464-1001A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45935506 | ||||||
| chr12:45935781
|
T | A | 23 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(20): Show | 28 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.464-1276A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45935781 | ||||||
| chr12:45935789
|
A | G | 3 | a0001c0006t0001g0241a0001c0006t0001g0242a0001c0006t0001g0243 | 3 | NA18951.hp2 NA18969.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.464-1284T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45935789 | ||||||
| chr12:45935888
|
GATCGTTT others(5): Show |
G | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 117 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.464-1395_464-1384d others(14): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45935888 | ||||||
| chr12:45936086
|
C | G | 1 | a0001c0001t0001g0152 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.464-1581G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936086 | ||||||
| chr12:45936102
|
A | G | 1 | a0001c0001t0003g0023 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.464-1597T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936102 | ||||||
| chr12:45936147
|
G | GT | 10 | a0001c0001t0001g0207a0001c0004t0003g0020a0001c0004t0003g0133others(7): Show | 11 | HG00597.hp1 HG02451.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.464-1643dupA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936147 | ||||||
| chr12:45936159
|
T | G | 1 | a0001c0001t0001g0297 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.464-1654A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936159 | ||||||
| chr12:45936236
|
G | C | 1 | a0007c0012t0002g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.464-1731C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936236 | ||||||
| chr12:45936248
|
T | G | 1 | a0001c0004t0003g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.464-1743A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936248 | ||||||
| chr12:45936291
|
A | C | 2 | a0001c0006t0001g0222a0001c0006t0001g0223 | 2 | HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.464-1786T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936291 | ||||||
| chr12:45936353
|
G | C | 1 | a0001c0001t0001g0146 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.464-1848C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936353 | ||||||
| chr12:45936393
|
C | T | 23 | a0001c0001t0001g0014a0001c0001t0001g0120a0001c0001t0001g0140others(20): Show | 24 | HG01109.hp2 HG01496.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.464-1888G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936393 | ||||||
| chr12:45936415
|
C | T | 154 | a0001c0001t0003g0274a0001c0001t0003g0290a0001c0001t0003g0291others(151): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.464-1910G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936415 | ||||||
| chr12:45936627
|
T | C | 1 | a0002c0003t0002g0100 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.464-2122A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936627 | ||||||
| chr12:45936666
|
T | C | 1 | a0002c0002t0002g0082 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.464-2161A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936666 | ||||||
| chr12:45936669
|
AAT | A | 4 | a0002c0002t0002g0050a0002c0002t0002g0051a0002c0002t0002g0053others(1): Show | 4 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-2166_464-2165d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936669 | ||||||
| chr12:45936779
|
T | G | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.464-2274A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936779 | ||||||
| chr12:45936975
|
TC | T | 23 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(20): Show | 28 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.464-2471delG | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45936975 | ||||||
| chr12:45937147
|
A | G | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-2642T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45937147 | ||||||
| chr12:45937213
|
C | G | 1 | a0002c0002t0002g0010 | 2 | HG02165.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.464-2708G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45937213 | ||||||
| chr12:45937308
|
G | A | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-2803C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45937308 | ||||||
| chr12:45937704
|
T | C | 16 | a0002c0002t0002g0001a0002c0002t0002g0007a0002c0002t0002g0045others(13): Show | 20 | HG00438.hp2 HG00621.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.464-3199A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45937704 | ||||||
| chr12:45937730
|
A | G | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-3225T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45937730 | ||||||
| chr12:45937859
|
C | T | 1 | a0002c0002t0002g0122 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.464-3354G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45937859 | ||||||
| chr12:45938049
|
TC | T | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-3545delG | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45938049 | ||||||
| chr12:45938345
|
C | T | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(92): Show | 103 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.464-3840G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45938345 | ||||||
| chr12:45938357
|
C | T | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-3852G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45938357 | ||||||
| chr12:45938420
|
C | T | 4 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(1): Show | 5 | HG01109.hp1 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-3915G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45938420 | ||||||
| chr12:45938471
|
A | G | 1 | a0002c0003t0002g0107 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.464-3966T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45938471 | ||||||
| chr12:45938501
|
CAA | C | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 117 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.464-3998_464-3997d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45938501 | ||||||
| chr12:45938714
|
G | A | 4 | a0002c0002t0002g0050a0002c0002t0002g0051a0002c0002t0002g0053others(1): Show | 4 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-4209C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45938714 | ||||||
| chr12:45939261
|
C | A | 1 | a0005c0009t0001g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.464-4756G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45939261 | ||||||
| chr12:45939378
|
C | A | 3 | a0002c0002t0003g0128a0002c0002t0003g0276a0002c0019t0003g0296 | 3 | HG01884.hp1 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.464-4873G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45939378 | ||||||
| chr12:45939466
|
C | T | 23 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(20): Show | 28 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.464-4961G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45939466 | ||||||
| chr12:45939506
|
A | C | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-5001T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45939506 | ||||||
| chr12:45939525
|
CCT | C | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-5022_464-5021d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45939525 | ||||||
| chr12:45939589
|
T | C | 3 | a0001c0007t0003g0022a0001c0007t0003g0293a0001c0007t0003g0294 | 4 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-5084A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45939589 | ||||||
| chr12:45939630
|
G | A | 4 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(1): Show | 5 | HG01109.hp1 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-5125C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45939630 | ||||||
| chr12:45939646
|
CGAGATCG others(7): Show |
C | 1 | a0002c0003t0002g0106 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.464-5155_464-5142d others(16): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45939646 | ||||||
| chr12:45939733
|
A | C | 1 | a0002c0019t0003g0296 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.464-5228T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45939733 | ||||||
| chr12:45939816
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.464-5311A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45939816 | ||||||
| chr12:45940136
|
G | A | 1 | a0001c0001t0003g0023 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.463+5113C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45940136 | ||||||
| chr12:45940244
|
A | T | 1 | a0002c0002t0002g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.463+5005T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45940244 | ||||||
| chr12:45940486
|
G | A | 1 | a0018c0021t0002g0044 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.463+4763C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45940486 | ||||||
| chr12:45940599
|
A | C | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+4650T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45940599 | ||||||
| chr12:45940731
|
G | A | 1 | a0002c0002t0002g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.463+4518C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45940731 | ||||||
| chr12:45940897
|
C | T | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+4352G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45940897 | ||||||
| chr12:45940977
|
G | C | 1 | a0002c0003t0002g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.463+4272C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45940977 | ||||||
| chr12:45940991
|
G | A | 2 | a0002c0002t0002g0030a0002c0002t0002g0033 | 2 | NA18957.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.463+4258C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45940991 | ||||||
| chr12:45941049
|
C | T | 107 | a0002c0002t0002g0001a0002c0002t0002g0007a0002c0002t0002g0009others(104): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.463+4200G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45941049 | ||||||
| chr12:45941132
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.463+4117T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45941132 | ||||||
| chr12:45941197
|
A | C | 1 | a0002c0002t0002g0075 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.463+4052T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45941197 | ||||||
| chr12:45941234
|
C | T | 1 | a0002c0003t0018g0037 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.463+4015G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45941234 | ||||||
| chr12:45941251
|
T | C | 2 | a0001c0001t0003g0180a0001c0001t0003g0188 | 2 | NA18957.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.463+3998A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45941251 | ||||||
| chr12:45941252
|
C | T | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+3997G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45941252 | ||||||
| chr12:45941341
|
C | T | 268 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(265): Show | 294 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.463+3908G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45941341 | ||||||
| chr12:45941355
|
A | G | 1 | a0001c0001t0003g0169 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.463+3894T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45941355 | ||||||
| chr12:45941626
|
C | A | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 117 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.463+3623G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45941626 | ||||||
| chr12:45941827
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.463+3422C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45941827 | ||||||
| chr12:45942008
|
A | T | 1 | a0001c0001t0001g0140 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.463+3241T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45942008 | ||||||
| chr12:45942054
|
A | G | 2 | a0001c0001t0010g0309a0001c0001t0010g0310 | 2 | HG01346.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.463+3195T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45942054 | ||||||
| chr12:45942344
|
C | T | 2 | a0001c0001t0003g0193a0001c0001t0003g0299 | 2 | NA18951.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.463+2905G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45942344 | ||||||
| chr12:45942445
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.463+2804C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45942445 | ||||||
| chr12:45942475
|
G | A | 107 | a0002c0002t0002g0001a0002c0002t0002g0007a0002c0002t0002g0009others(104): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.463+2774C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45942475 | ||||||
| chr12:45942508
|
GCCCTAAA others(7): Show |
G | 1 | a0003c0005t0004g0025 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.463+2727_463+2740d others(16): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45942508 | ||||||
| chr12:45942591
|
TA | T | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+2657delT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45942591 | ||||||
| chr12:45942871
|
A | G | 1 | a0002c0003t0002g0098 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.463+2378T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45942871 | ||||||
| chr12:45942964
|
T | TGA | 31 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(28): Show | 38 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.463+2283_463+2284d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45942964 | ||||||
| chr12:45943019
|
C | G | 2 | a0002c0002t0002g0078a0002c0002t0002g0113 | 2 | HG01192.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.463+2230G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45943019 | ||||||
| chr12:45943137
|
T | C | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.463+2112A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45943137 | ||||||
| chr12:45943594
|
TAGTTTCA others(3): Show |
T | 2 | a0001c0001t0010g0309a0001c0001t0010g0310 | 2 | HG01346.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.463+1645_463+1654d others(12): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45943594 | ||||||
| chr12:45943660
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.463+1589A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45943660 | ||||||
| chr12:45943900
|
C | A | 2 | a0001c0015t0001g0249a0001c0015t0001g0250 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.463+1349G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45943900 | ||||||
| chr12:45944161
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.463+1088A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45944161 | ||||||
| chr12:45944229
|
T | C | 2 | a0001c0001t0001g0269a0001c0001t0003g0203 | 2 | HG01993.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.463+1020A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45944229 | ||||||
| chr12:45944266
|
A | G | 1 | a0001c0001t0003g0184 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.463+983T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45944266 | ||||||
| chr12:45944297
|
C | T | 31 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0011others(28): Show | 35 | HG00609.hp1 HG01515.hp1 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.463+952G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45944297 | ||||||
| chr12:45944297
|
CCA | C | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+950_463+951del others(2): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45944297 | ||||||
| chr12:45944330
|
C | T | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.463+919G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45944330 | ||||||
| chr12:45944534
|
G | A | 1 | a0001c0001t0011g0261 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.463+715C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45944534 | ||||||
| chr12:45944591
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.463+658C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45944591 | ||||||
| chr12:45944636
|
C | T | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+613G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45944636 | ||||||
| chr12:45944786
|
CT | C | 268 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(265): Show | 294 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.463+462delA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45944786 | ||||||
| chr12:45945061
|
G | A | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+188C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45945061 | ||||||
| chr12:45945209
|
CA | C | 23 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(20): Show | 28 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.463+39delT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45945209 | ||||||
| chr12:45945216
|
A | G | 1 | a0001c0001t0013g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.463+33T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 6/14 | chr12 | 45945216 | ||||||
| chr12:45945400
|
A | G | 3 | a0001c0007t0003g0022a0001c0007t0003g0293a0001c0007t0003g0294 | 4 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.399-87T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45945400 | ||||||
| chr12:45945529
|
T | C | 2 | a0001c0001t0003g0180a0001c0001t0003g0188 | 2 | NA18957.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.399-216A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45945529 | ||||||
| chr12:45945536
|
C | CT | 14 | a0001c0001t0001g0210a0001c0001t0001g0297a0002c0002t0002g0009others(11): Show | 16 | HG00140.hp2 HG01071.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.399-224dupA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45945536 | ||||||
| chr12:45945536
|
CT | C | 44 | a0001c0001t0001g0166a0001c0001t0001g0228a0001c0001t0003g0186others(41): Show | 51 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.399-224delA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45945536 | ||||||
| chr12:45945920
|
G | T | 1 | a0002c0002t0017g0072 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.399-607C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45945920 | ||||||
| chr12:45945929
|
C | T | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.399-616G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45945929 | ||||||
| chr12:45945982
|
C | A | 1 | a0002c0002t0003g0276 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.399-669G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45945982 | ||||||
| chr12:45946044
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.399-731A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45946044 | ||||||
| chr12:45946123
|
A | G | 1 | a0002c0003t0007g0105 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.399-810T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45946123 | ||||||
| chr12:45946200
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.399-887G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45946200 | ||||||
| chr12:45946382
|
G | T | 1 | a0002c0002t0002g0060 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.399-1069C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45946382 | ||||||
| chr12:45946641
|
GA | G | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(107): Show | 118 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.399-1329delT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45946641 | ||||||
| chr12:45946880
|
G | A | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.398+1557C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45946880 | ||||||
| chr12:45946955
|
C | G | 105 | a0002c0002t0002g0001a0002c0002t0002g0007a0002c0002t0002g0009others(102): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.398+1482G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45946955 | ||||||
| chr12:45947018
|
T | C | 1 | a0002c0002t0002g0087 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.398+1419A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45947018 | ||||||
| chr12:45947038
|
A | G | 310 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(307): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.398+1399T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45947038 | ||||||
| chr12:45947422
|
T | A | 1 | a0001c0001t0003g0292 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.398+1015A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45947422 | ||||||
| chr12:45947445
|
T | C | 3 | a0001c0001t0001g0142a0001c0001t0001g0155a0001c0001t0001g0163 | 3 | HG02074.hp2 HG02523.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.398+992A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45947445 | ||||||
| chr12:45947746
|
A | G | 2 | a0001c0007t0003g0022a0001c0007t0003g0293 | 3 | HG01167.hp2 HG01169.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.398+691T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45947746 | ||||||
| chr12:45947809
|
T | G | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.398+628A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45947809 | ||||||
| chr12:45947827
|
T | C | 1 | a0001c0001t0003g0201 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.398+610A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45947827 | ||||||
| chr12:45947970
|
C | A | 1 | a0001c0001t0001g0206 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.398+467G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45947970 | ||||||
| chr12:45947984
|
A | C | 1 | a0002c0002t0002g0081 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.398+453T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45947984 | ||||||
| chr12:45948060
|
A | G | 24 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(21): Show | 29 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.398+377T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45948060 | ||||||
| chr12:45948061
|
C | G | 1 | a0002c0003t0002g0095 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.398+376G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45948061 | ||||||
| chr12:45948084
|
T | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 117 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.398+353A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45948084 | ||||||
| chr12:45948213
|
G | C | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.398+224C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45948213 | ||||||
| chr12:45948243
|
C | T | 1 | a0002c0003t0002g0095 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.398+194G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 5/14 | chr12 | 45948243 | ||||||
| chr12:45948541
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG02970.hp2 | splice_region_variant&intron_variant | LOW | c.298-4A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45948541 | ||||||
| chr12:45948635
|
T | C | 1 | a0001c0001t0003g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.298-98A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45948635 | ||||||
| chr12:45948771
|
C | T | 2 | a0001c0004t0003g0272a0001c0004t0003g0273 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.298-234G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45948771 | ||||||
| chr12:45948777
|
T | G | 2 | a0001c0001t0003g0180a0001c0001t0003g0188 | 2 | NA18957.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.298-240A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45948777 | ||||||
| chr12:45948779
|
T | C | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.298-242A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45948779 | ||||||
| chr12:45949093
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0246 | 2 | HG01106.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.298-556G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45949093 | ||||||
| chr12:45949129
|
T | C | 1 | a0003c0005t0004g0028 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.298-592A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45949129 | ||||||
| chr12:45949155
|
C | T | 2 | a0001c0001t0003g0180a0001c0001t0003g0188 | 2 | NA18957.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.298-618G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45949155 | ||||||
| chr12:45949181
|
AACTAGAT others(24): Show |
A | 1 | a0001c0001t0001g0158 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.298-675_298-645del others(31): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45949181 | ||||||
| chr12:45949301
|
C | T | 2 | a0001c0004t0003g0129a0001c0004t0003g0270 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.298-764G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45949301 | ||||||
| chr12:45949306
|
G | A | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-769C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45949306 | ||||||
| chr12:45949641
|
A | C | 6 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0227others(3): Show | 6 | NA18940.hp1 NA18947.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-1104T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45949641 | ||||||
| chr12:45950027
|
T | TCATA | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-1494_298-1491d others(6): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45950027 | ||||||
| chr12:45950091
|
C | T | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-1554G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45950091 | ||||||
| chr12:45950124
|
C | T | 4 | a0001c0006t0001g0241a0001c0006t0001g0242a0001c0006t0001g0243others(1): Show | 4 | HG04199.hp2 NA18951.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+1526G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45950124 | ||||||
| chr12:45950142
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.297+1508C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45950142 | ||||||
| chr12:45950199
|
T | C | 2 | a0001c0007t0003g0022a0001c0007t0003g0293 | 3 | HG01167.hp2 HG01169.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.297+1451A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45950199 | ||||||
| chr12:45950480
|
A | G | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+1170T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45950480 | ||||||
| chr12:45950710
|
T | A | 1 | a0002c0002t0003g0276 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.297+940A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45950710 | ||||||
| chr12:45950864
|
G | C | 1 | a0002c0003t0002g0100 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.297+786C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45950864 | ||||||
| chr12:45950866
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.297+784A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45950866 | ||||||
| chr12:45950932
|
T | G | 65 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(62): Show | 70 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.297+718A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45950932 | ||||||
| chr12:45951040
|
T | C | 1 | a0002c0002t0002g0121 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.297+610A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45951040 | ||||||
| chr12:45951096
|
T | C | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+554A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45951096 | ||||||
| chr12:45951146
|
T | C | 1 | a0001c0001t0003g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.297+504A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45951146 | ||||||
| chr12:45951180
|
A | C | 2 | a0001c0001t0010g0309a0001c0001t0010g0310 | 2 | HG01346.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.297+470T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45951180 | ||||||
| chr12:45951196
|
T | C | 31 | a0002c0003t0002g0012a0002c0003t0002g0013a0002c0003t0002g0036others(28): Show | 33 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.297+454A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45951196 | ||||||
| chr12:45951300
|
C | G | 310 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(307): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.297+350G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45951300 | ||||||
| chr12:45951367
|
C | T | 6 | a0001c0001t0001g0143a0001c0001t0001g0157a0001c0001t0001g0297others(3): Show | 6 | HG04184.hp2 NA18953.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.297+283G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45951367 | ||||||
| chr12:45951381
|
G | A | 1 | a0002c0003t0002g0036 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.297+269C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45951381 | ||||||
| chr12:45951390
|
A | T | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+260T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45951390 | ||||||
| chr12:45951474
|
G | A | 5 | a0001c0004t0003g0002a0001c0004t0003g0021a0001c0004t0003g0284others(2): Show | 9 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+176C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45951474 | ||||||
| chr12:45951526
|
A | G | 1 | a0003c0005t0006g0135 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.297+124T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 4/14 | chr12 | 45951526 | ||||||
| chr12:45951935
|
A | T | 1 | a0009c0014t0003g0024 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.220-208T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45951935 | ||||||
| chr12:45951990
|
A | G | 1 | a0001c0001t0003g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-263T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45951990 | ||||||
| chr12:45952010
|
C | T | 1 | a0002c0002t0003g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.220-283G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45952010 | ||||||
| chr12:45952109
|
G | C | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-382C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45952109 | ||||||
| chr12:45952207
|
C | T | 1 | a0001c0001t0003g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-480G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45952207 | ||||||
| chr12:45952372
|
A | G | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-645T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45952372 | ||||||
| chr12:45952530
|
T | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0154a0001c0001t0001g0158others(4): Show | 8 | HG01109.hp2 HG01496.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.220-803A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45952530 | ||||||
| chr12:45952593
|
T | C | 3 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0221 | 3 | HG00280.hp1 HG00741.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.220-866A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45952593 | ||||||
| chr12:45952616
|
T | C | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-889A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45952616 | ||||||
| chr12:45952658
|
A | T | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-931T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45952658 | ||||||
| chr12:45953042
|
T | A | 1 | a0001c0001t0003g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-1315A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45953042 | ||||||
| chr12:45953206
|
T | G | 2 | a0002c0010t0002g0115a0002c0010t0002g0127 | 2 | NA18970.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.220-1479A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45953206 | ||||||
| chr12:45953266
|
T | C | 1 | a0001c0001t0003g0301 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220-1539A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45953266 | ||||||
| chr12:45953341
|
G | A | 107 | a0002c0002t0002g0001a0002c0002t0002g0007a0002c0002t0002g0009others(104): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.220-1614C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45953341 | ||||||
| chr12:45953538
|
C | T | 1 | a0001c0001t0003g0023 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.220-1811G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45953538 | ||||||
| chr12:45953641
|
A | G | 2 | a0001c0004t0003g0272a0001c0004t0003g0273 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.220-1914T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45953641 | ||||||
| chr12:45954024
|
T | A | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.220-2297A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954024 | ||||||
| chr12:45954195
|
T | A | 1 | a0001c0001t0003g0169 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.220-2468A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954195 | ||||||
| chr12:45954293
|
A | G | 154 | a0001c0001t0003g0274a0001c0001t0003g0290a0001c0001t0003g0291others(151): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.220-2566T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954293 | ||||||
| chr12:45954304
|
T | C | 2 | a0001c0004t0003g0288a0001c0004t0003g0289 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.220-2577A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954304 | ||||||
| chr12:45954374
|
C | T | 1 | a0002c0003t0002g0012 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.220-2647G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954374 | ||||||
| chr12:45954426
|
G | A | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-2699C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954426 | ||||||
| chr12:45954557
|
T | C | 1 | a0001c0001t0003g0204 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.220-2830A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954557 | ||||||
| chr12:45954569
|
CT | C | 15 | a0001c0001t0003g0023a0001c0001t0003g0173a0001c0001t0003g0185others(12): Show | 16 | HG01081.hp2 HG01167.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.220-2843delA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954569 | ||||||
| chr12:45954614
|
C | T | 8 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(5): Show | 8 | HG02615.hp1 HG02738.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-2887G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954614 | ||||||
| chr12:45954706
|
G | C | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-2979C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954706 | ||||||
| chr12:45954712
|
T | G | 1 | a0001c0001t0003g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-2985A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954712 | ||||||
| chr12:45954728
|
CCTAG | C | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-3005_220-3002d others(6): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954728 | ||||||
| chr12:45954733
|
C | CT | 126 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(123): Show | 141 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.220-3007dupA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954733 | ||||||
| chr12:45954733
|
C | CTT | 23 | a0001c0001t0001g0131a0001c0001t0001g0151a0001c0001t0001g0253others(20): Show | 24 | HG00408.hp1 HG01109.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.220-3008_220-3007d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954733 | ||||||
| chr12:45954733
|
CT | C | 8 | a0001c0001t0003g0016a0001c0001t0003g0195a0001c0001t0003g0203others(5): Show | 9 | HG01069.hp2 HG01071.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-3007delA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954733 | ||||||
| chr12:45954937
|
C | G | 2 | a0001c0015t0001g0249a0001c0015t0001g0250 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.220-3210G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954937 | ||||||
| chr12:45954939
|
C | CT | 106 | a0001c0001t0014g0168a0002c0002t0002g0001a0002c0002t0002g0007others(103): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.220-3213dupA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45954939 | ||||||
| chr12:45955005
|
G | C | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-3278C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45955005 | ||||||
| chr12:45955076
|
T | C | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 117 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.220-3349A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45955076 | ||||||
| chr12:45955194
|
C | T | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.220-3467G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45955194 | ||||||
| chr12:45955217
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.220-3490G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45955217 | ||||||
| chr12:45955425
|
C | A | 3 | a0001c0006t0001g0222a0001c0006t0001g0223a0001c0006t0001g0264 | 3 | HG01167.hp1 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.220-3698G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45955425 | ||||||
| chr12:45955596
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.220-3869G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45955596 | ||||||
| chr12:45955815
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.220-4088A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45955815 | ||||||
| chr12:45955955
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0230a0001c0001t0001g0231 | 5 | NA18747.hp2 NA18956.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-4228C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45955955 | ||||||
| chr12:45956138
|
C | T | 1 | a0002c0002t0002g0082 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.220-4411G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45956138 | ||||||
| chr12:45956197
|
G | C | 3 | a0001c0001t0003g0015a0001c0001t0003g0183a0001c0001t0003g0308 | 4 | HG00597.hp2 NA18945.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-4470C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45956197 | ||||||
| chr12:45956259
|
A | G | 2 | a0001c0001t0010g0309a0001c0001t0010g0310 | 2 | HG01346.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.220-4532T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45956259 | ||||||
| chr12:45956329
|
A | G | 1 | a0002c0002t0002g0087 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.220-4602T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45956329 | ||||||
| chr12:45956401
|
G | A | 1 | a0002c0003t0002g0095 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.220-4674C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45956401 | ||||||
| chr12:45956560
|
G | A | 2 | a0006c0011t0002g0008a0006c0011t0002g0112 | 3 | HG04184.hp1 NA19077.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.220-4833C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45956560 | ||||||
| chr12:45956807
|
A | C | 1 | a0001c0001t0003g0023 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.219+4893T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45956807 | ||||||
| chr12:45956986
|
T | C | 2 | a0001c0001t0003g0180a0001c0001t0003g0188 | 2 | NA18957.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.219+4714A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45956986 | ||||||
| chr12:45957030
|
C | T | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+4670G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45957030 | ||||||
| chr12:45957168
|
C | T | 10 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(7): Show | 10 | HG02451.hp2 HG02647.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.219+4532G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45957168 | ||||||
| chr12:45957502
|
C | G | 1 | a0002c0002t0002g0042 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.219+4198G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45957502 | ||||||
| chr12:45957610
|
G | A | 1 | a0007c0012t0002g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.219+4090C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45957610 | ||||||
| chr12:45957610
|
G | C | 110 | a0001c0001t0003g0274a0001c0001t0010g0309a0001c0001t0010g0310others(107): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.219+4090C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45957610 | ||||||
| chr12:45957866
|
C | T | 24 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(21): Show | 29 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.219+3834G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45957866 | ||||||
| chr12:45957868
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.219+3832C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45957868 | ||||||
| chr12:45957903
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.219+3797A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45957903 | ||||||
| chr12:45958013
|
C | G | 1 | a0002c0003t0002g0100 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.219+3687G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958013 | ||||||
| chr12:45958014
|
C | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0154a0001c0001t0001g0158others(4): Show | 8 | HG01109.hp2 HG01496.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.219+3686G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958014 | ||||||
| chr12:45958046
|
A | G | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.219+3654T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958046 | ||||||
| chr12:45958138
|
C | T | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.219+3562G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958138 | ||||||
| chr12:45958422
|
A | T | 1 | a0001c0006t0001g0241 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.219+3278T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958422 | ||||||
| chr12:45958639
|
T | G | 64 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(61): Show | 68 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.219+3061A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958639 | ||||||
| chr12:45958726
|
C | T | 1 | a0002c0003t0002g0036 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.219+2974G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958726 | ||||||
| chr12:45958770
|
C | CTTTTTTT others(22): Show |
1 | a0016c0026t0003g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219+2929_219+2930i others(31): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958770 | ||||||
| chr12:45958772
|
G | T | 1 | a0016c0026t0003g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219+2928C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958772 | ||||||
| chr12:45958773
|
A | T | 1 | a0016c0026t0003g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219+2927T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958773 | ||||||
| chr12:45958774
|
C | T | 1 | a0016c0026t0003g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219+2926G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958774 | ||||||
| chr12:45958775
|
A | T | 1 | a0016c0026t0003g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219+2925T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958775 | ||||||
| chr12:45958776
|
TACCCAAA others(3): Show |
T | 1 | a0016c0026t0003g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219+2914_219+2923d others(12): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958776 | ||||||
| chr12:45958780
|
C | T | 266 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(263): Show | 291 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.219+2920G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958780 | ||||||
| chr12:45958914
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.219+2786G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45958914 | ||||||
| chr12:45959162
|
C | T | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+2538G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45959162 | ||||||
| chr12:45959253
|
CT | C | 5 | a0001c0006t0001g0241a0001c0006t0001g0242a0001c0006t0001g0243others(2): Show | 5 | HG02602.hp2 HG04199.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+2446delA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45959253 | ||||||
| chr12:45959342
|
G | T | 43 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(40): Show | 50 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(47): Show |
intron_variant | MODIFIER | c.219+2358C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45959342 | ||||||
| chr12:45959358
|
A | G | 1 | a0002c0002t0002g0057 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.219+2342T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45959358 | ||||||
| chr12:45959373
|
G | T | 2 | a0001c0004t0003g0272a0001c0004t0003g0273 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.219+2327C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45959373 | ||||||
| chr12:45959496
|
C | T | 105 | a0002c0002t0002g0001a0002c0002t0002g0007a0002c0002t0002g0009others(102): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.219+2204G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45959496 | ||||||
| chr12:45959667
|
A | G | 1 | a0001c0001t0003g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219+2033T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45959667 | ||||||
| chr12:45959667
|
A | T | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+2033T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45959667 | ||||||
| chr12:45959752
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.219+1948T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45959752 | ||||||
| chr12:45959966
|
G | C | 1 | a0019c0016t0002g0111 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.219+1734C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45959966 | ||||||
| chr12:45960076
|
T | G | 17 | a0001c0001t0001g0120a0002c0002t0002g0001a0002c0002t0002g0007others(14): Show | 21 | HG00438.hp2 HG00621.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.219+1624A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45960076 | ||||||
| chr12:45960138
|
G | A | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.219+1562C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45960138 | ||||||
| chr12:45960425
|
T | C | 2 | a0001c0001t0010g0309a0001c0001t0010g0310 | 2 | HG01346.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219+1275A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45960425 | ||||||
| chr12:45960526
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.219+1174A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45960526 | ||||||
| chr12:45960757
|
A | T | 1 | a0002c0002t0002g0031 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.219+943T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45960757 | ||||||
| chr12:45960850
|
T | C | 24 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(21): Show | 29 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.219+850A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45960850 | ||||||
| chr12:45960983
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.219+717T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45960983 | ||||||
| chr12:45961154
|
T | C | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+546A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45961154 | ||||||
| chr12:45961482
|
T | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0231 | 2 | NA18747.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.219+218A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45961482 | ||||||
| chr12:45961483
|
A | T | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+217T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 3/14 | chr12 | 45961483 | ||||||
| chr12:45962015
|
G | A | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.62-158C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45962015 | ||||||
| chr12:45962294
|
T | C | 1 | a0001c0001t0003g0023 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.62-437A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45962294 | ||||||
| chr12:45962753
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.62-896A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45962753 | ||||||
| chr12:45962868
|
T | C | 105 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(102): Show | 113 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.62-1011A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45962868 | ||||||
| chr12:45962924
|
T | G | 1 | a0002c0002t0002g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.62-1067A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45962924 | ||||||
| chr12:45963150
|
C | T | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.61+957G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45963150 | ||||||
| chr12:45963190
|
A | G | 1 | a0001c0001t0011g0261 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.61+917T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45963190 | ||||||
| chr12:45963326
|
C | T | 1 | a0002c0003t0002g0099 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.61+781G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45963326 | ||||||
| chr12:45963336
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.61+771T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45963336 | ||||||
| chr12:45963438
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.61+669A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45963438 | ||||||
| chr12:45963457
|
GA | G | 5 | a0001c0004t0003g0002a0001c0004t0003g0021a0001c0004t0003g0284others(2): Show | 9 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+649delT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45963457 | ||||||
| chr12:45963461
|
A | T | 1 | a0001c0001t0001g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.61+646T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45963461 | ||||||
| chr12:45963927
|
T | A | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+180A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45963927 | ||||||
| chr12:45963931
|
T | C | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+176A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 2/14 | chr12 | 45963931 | ||||||
| chr12:45964301
|
G | A | 1 | a0003c0005t0004g0028 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-21-113C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45964301 | ||||||
| chr12:45964666
|
C | CA | 9 | a0001c0004t0003g0002a0001c0004t0003g0021a0001c0004t0003g0284others(6): Show | 13 | HG01993.hp1 HG02083.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-21-479dupT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45964666 | ||||||
| chr12:45964699
|
T | A | 1 | a0001c0001t0003g0204 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-21-511A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45964699 | ||||||
| chr12:45964699
|
T | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0263 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-511A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45964699 | ||||||
| chr12:45964762
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-21-574G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45964762 | ||||||
| chr12:45964886
|
C | T | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-21-698G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45964886 | ||||||
| chr12:45964928
|
A | AGTGT | 24 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(21): Show | 29 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.-21-744_-21-741dup others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45964928 | ||||||
| chr12:45965081
|
A | T | 4 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(1): Show | 5 | HG01109.hp1 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-893T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45965081 | ||||||
| chr12:45965191
|
T | A | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(105): Show | 116 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-21-1003A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45965191 | ||||||
| chr12:45965340
|
G | A | 3 | a0005c0009t0001g0147a0005c0009t0001g0148a0005c0009t0001g0167 | 3 | NA18967.hp1 NA18983.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-21-1152C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45965340 | ||||||
| chr12:45965512
|
CTG | C | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-1326_-21-1325d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45965512 | ||||||
| chr12:45965525
|
G | A | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-1337C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45965525 | ||||||
| chr12:45965695
|
C | T | 2 | a0001c0001t0014g0168a0002c0002t0002g0063 | 2 | NA18941.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-21-1507G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45965695 | ||||||
| chr12:45965742
|
T | TCTGAATG others(332): Show |
1 | a0001c0006t0001g0252 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-21-1555_-21-1554i others(341): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45965742 | ||||||
| chr12:45966041
|
C | T | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(105): Show | 116 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-21-1853G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45966041 | ||||||
| chr12:45966049
|
A | T | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(105): Show | 116 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-21-1861T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45966049 | ||||||
| chr12:45966245
|
A | C | 1 | a0005c0009t0001g0149 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-21-2057T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45966245 | ||||||
| chr12:45966305
|
T | C | 1 | a0016c0026t0003g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-21-2117A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45966305 | ||||||
| chr12:45966332
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-21-2144A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45966332 | ||||||
| chr12:45966388
|
G | C | 1 | a0002c0003t0002g0036 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-21-2200C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45966388 | ||||||
| chr12:45966634
|
G | A | 9 | a0001c0006t0001g0222a0001c0006t0001g0223a0001c0006t0001g0241others(6): Show | 9 | HG01167.hp1 HG02602.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-2446C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45966634 | ||||||
| chr12:45967058
|
T | C | 1 | a0001c0004t0003g0273 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-21-2870A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45967058 | ||||||
| chr12:45967081
|
A | G | 1 | a0001c0001t0003g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-21-2893T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45967081 | ||||||
| chr12:45967113
|
T | G | 1 | a0002c0019t0003g0296 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-21-2925A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45967113 | ||||||
| chr12:45967154
|
G | A | 1 | a0002c0002t0002g0121 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-21-2966C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45967154 | ||||||
| chr12:45967236
|
T | C | 106 | a0001c0001t0001g0120a0002c0002t0002g0001a0002c0002t0002g0007others(103): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-21-3048A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45967236 | ||||||
| chr12:45967348
|
A | T | 1 | a0002c0003t0002g0096 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-21-3160T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45967348 | ||||||
| chr12:45967605
|
C | T | 2 | a0001c0001t0003g0180a0001c0001t0003g0188 | 2 | NA18957.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-21-3417G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45967605 | ||||||
| chr12:45967657
|
T | A | 2 | a0008c0013t0001g0225a0008c0013t0001g0226 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-21-3469A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45967657 | ||||||
| chr12:45967675
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-21-3487A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45967675 | ||||||
| chr12:45967889
|
C | A | 74 | a0002c0002t0002g0001a0002c0002t0002g0007a0002c0002t0002g0009others(71): Show | 82 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-21-3701G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45967889 | ||||||
| chr12:45968255
|
T | C | 1 | a0001c0001t0001g0214 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-21-4067A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45968255 | ||||||
| chr12:45968419
|
T | C | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-4231A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45968419 | ||||||
| chr12:45968420
|
G | A | 1 | a0003c0005t0004g0029 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-21-4232C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45968420 | ||||||
| chr12:45968548
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-21-4360G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45968548 | ||||||
| chr12:45968642
|
T | C | 1 | a0002c0002t0002g0076 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-21-4454A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45968642 | ||||||
| chr12:45968716
|
G | A | 1 | a0002c0002t0002g0030 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-21-4528C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45968716 | ||||||
| chr12:45968772
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0263 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-21-4584G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45968772 | ||||||
| chr12:45968803
|
G | A | 2 | a0001c0001t0010g0309a0001c0001t0010g0310 | 2 | HG01346.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-21-4615C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45968803 | ||||||
| chr12:45968863
|
T | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0154a0001c0001t0001g0158others(4): Show | 8 | HG01109.hp2 HG01496.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21-4675A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45968863 | ||||||
| chr12:45968874
|
C | T | 1 | a0002c0002t0002g0088 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-21-4686G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45968874 | ||||||
| chr12:45969244
|
G | T | 268 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(265): Show | 294 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.-21-5056C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45969244 | ||||||
| chr12:45969278
|
T | C | 2 | a0001c0015t0001g0249a0001c0015t0001g0250 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-21-5090A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45969278 | ||||||
| chr12:45969474
|
C | T | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-5286G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45969474 | ||||||
| chr12:45969885
|
C | T | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-21-5697G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45969885 | ||||||
| chr12:45969905
|
T | G | 4 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(1): Show | 5 | HG01109.hp1 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-5717A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45969905 | ||||||
| chr12:45969929
|
G | A | 1 | a0001c0001t0003g0292 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-21-5741C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45969929 | ||||||
| chr12:45969983
|
G | A | 1 | a0002c0002t0002g0077 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-21-5795C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45969983 | ||||||
| chr12:45970061
|
A | T | 1 | a0001c0001t0001g0266 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-21-5873T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45970061 | ||||||
| chr12:45970141
|
G | A | 1 | a0001c0001t0003g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-21-5953C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45970141 | ||||||
| chr12:45970692
|
G | A | 1 | a0003c0005t0006g0134 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21-6504C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45970692 | ||||||
| chr12:45970797
|
C | T | 1 | a0002c0002t0002g0059 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-21-6609G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45970797 | ||||||
| chr12:45971114
|
T | C | 1 | a0002c0019t0003g0296 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-21-6926A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45971114 | ||||||
| chr12:45971168
|
T | C | 1 | a0001c0004t0003g0287 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-21-6980A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45971168 | ||||||
| chr12:45971195
|
G | A | 1 | a0002c0003t0002g0106 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-21-7007C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45971195 | ||||||
| chr12:45971296
|
T | A | 2 | a0001c0004t0009g0282a0001c0004t0009g0283 | 2 | HG01175.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-21-7108A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45971296 | ||||||
| chr12:45971359
|
A | G | 1 | a0002c0002t0003g0276 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-21-7171T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45971359 | ||||||
| chr12:45971457
|
T | C | 1 | a0001c0001t0003g0023 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-21-7269A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45971457 | ||||||
| chr12:45971647
|
G | A | 1 | a0001c0001t0003g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-21-7459C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45971647 | ||||||
| chr12:45971745
|
C | A | 1 | a0005c0009t0001g0149 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-21-7557G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45971745 | ||||||
| chr12:45971775
|
T | C | 1 | a0009c0014t0003g0024 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-21-7587A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45971775 | ||||||
| chr12:45972036
|
G | A | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-21-7848C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972036 | ||||||
| chr12:45972097
|
C | T | 1 | a0002c0002t0002g0083 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-21-7909G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972097 | ||||||
| chr12:45972118
|
A | G | 1 | a0001c0004t0009g0282 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-21-7930T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972118 | ||||||
| chr12:45972575
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-21-8387G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972575 | ||||||
| chr12:45972585
|
T | TA | 15 | a0001c0004t0003g0281a0001c0007t0003g0022a0001c0007t0003g0293others(12): Show | 17 | HG00140.hp2 HG01123.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-21-8398dupT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972585 | ||||||
| chr12:45972585
|
TA | T | 103 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(100): Show | 111 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-21-8398delT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972585 | ||||||
| chr12:45972585
|
TAA | T | 12 | a0001c0001t0001g0150a0001c0001t0001g0219a0001c0001t0001g0233others(9): Show | 12 | HG01074.hp2 HG02129.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-8399_-21-8398d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972585 | ||||||
| chr12:45972599
|
A | G | 1 | a0003c0005t0004g0026 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-21-8411T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972599 | ||||||
| chr12:45972638
|
T | C | 1 | a0015c0024t0001g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21-8450A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972638 | ||||||
| chr12:45972773
|
A | C | 1 | a0003c0005t0006g0134 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21-8585T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972773 | ||||||
| chr12:45972779
|
C | T | 1 | a0002c0003t0002g0126 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-21-8591G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972779 | ||||||
| chr12:45972788
|
T | C | 10 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(7): Show | 10 | HG02451.hp2 HG02647.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21-8600A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972788 | ||||||
| chr12:45972848
|
G | GTA | 11 | a0001c0001t0003g0003a0001c0001t0003g0015a0001c0001t0003g0173others(8): Show | 14 | HG00597.hp2 HG00673.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21-8662_-21-8661d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972848 | ||||||
| chr12:45972864
|
CGATATAT others(21): Show |
C | 10 | a0001c0001t0001g0212a0001c0001t0003g0023a0001c0001t0003g0178others(7): Show | 11 | HG00639.hp2 HG01081.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21-8704_-21-8677d others(30): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972864 | ||||||
| chr12:45972865
|
GAT | G | 35 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0145others(32): Show | 38 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.-21-8679_-21-8678d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972865 | ||||||
| chr12:45972865
|
GATATATA others(23): Show |
G | 77 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(74): Show | 82 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.-21-8707_-21-8678d others(32): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972865 | ||||||
| chr12:45972869
|
TATATATA others(53): Show |
T | 1 | a0001c0006t0001g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-21-8741_-21-8682d others(62): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972869 | ||||||
| chr12:45972875
|
TATATAGA others(11): Show |
T | 4 | a0003c0005t0004g0026a0003c0005t0004g0027a0003c0005t0004g0028others(1): Show | 4 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-8705_-21-8688d others(20): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972875 | ||||||
| chr12:45972876
|
A | C | 4 | a0001c0004t0003g0020a0001c0004t0003g0133a0001c0004t0003g0295others(1): Show | 5 | HG00738.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-8688T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972876 | ||||||
| chr12:45972880
|
A | C | 3 | a0001c0001t0003g0301a0001c0004t0003g0129a0002c0002t0002g0061 | 3 | HG02717.hp1 HG02922.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-21-8692T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972880 | ||||||
| chr12:45972881
|
GATATATA others(9): Show |
G | 1 | a0003c0005t0004g0025 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-21-8709_-21-8694d others(18): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972881 | ||||||
| chr12:45972883
|
TATATATA others(39): Show |
T | 3 | a0001c0007t0003g0294a0001c0007t0008g0306a0001c0007t0008g0307 | 3 | HG02559.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-21-8741_-21-8696d others(48): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972883 | ||||||
| chr12:45972887
|
TATATAG | T | 4 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(1): Show | 5 | HG01109.hp1 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-8705_-21-8700d others(8): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972887 | ||||||
| chr12:45972892
|
A | C | 2 | a0001c0001t0001g0218a0001c0001t0003g0190 | 2 | HG00280.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.-21-8704T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972892 | ||||||
| chr12:45972893
|
GAT | G | 5 | a0001c0001t0003g0174a0001c0001t0003g0184a0001c0001t0003g0193others(2): Show | 5 | HG00099.hp2 HG01993.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-8707_-21-8706d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972893 | ||||||
| chr12:45972893
|
GATATATA others(31): Show |
G | 22 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0145others(19): Show | 25 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-21-8743_-21-8706d others(40): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972893 | ||||||
| chr12:45972897
|
T | G | 8 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(5): Show | 9 | HG01109.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-8709A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972897 | ||||||
| chr12:45972897
|
T | TATATATA others(79): Show |
2 | a0001c0004t0003g0272a0001c0004t0003g0273 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-21-8710_-21-8709i others(88): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972897 | ||||||
| chr12:45972897
|
T | TATATATA others(17): Show |
1 | a0001c0004t0003g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-21-8710_-21-8709i others(26): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972897 | ||||||
| chr12:45972897
|
T | TATATATA others(41): Show |
16 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(13): Show | 21 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-21-8710_-21-8709i others(50): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972897 | ||||||
| chr12:45972897
|
TATATATA others(25): Show |
T | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-8741_-21-8710d others(34): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972897 | ||||||
| chr12:45972898
|
A | ATATATAG others(9): Show |
5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-8711_-21-8710i others(18): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972898 | ||||||
| chr12:45972899
|
T | G | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-21-8711A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972899 | ||||||
| chr12:45972899
|
T | TAG | 113 | a0001c0001t0001g0120a0001c0001t0001g0224a0001c0001t0001g0240others(110): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.-21-8712_-21-8711i others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972899 | ||||||
| chr12:45972900
|
A | C | 1 | a0016c0026t0003g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-21-8712T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972900 | ||||||
| chr12:45972901
|
T | G | 2 | a0008c0013t0001g0225a0008c0013t0001g0226 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-21-8713A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972901 | ||||||
| chr12:45972901
|
T | TATAG | 4 | a0001c0004t0003g0129a0001c0004t0003g0270a0001c0004t0003g0271others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-8714_-21-8713i others(6): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972901 | ||||||
| chr12:45972903
|
T | G | 1 | a0002c0003t0002g0107 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-21-8715A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972903 | ||||||
| chr12:45972903
|
TATATAGA others(19): Show |
T | 2 | a0001c0007t0003g0022a0001c0007t0003g0293 | 3 | HG01167.hp2 HG01169.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-21-8741_-21-8716d others(28): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972903 | ||||||
| chr12:45972903
|
TATATAGA others(41): Show |
T | 2 | a0008c0013t0001g0225a0008c0013t0001g0226 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-21-8763_-21-8716d others(50): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972903 | ||||||
| chr12:45972915
|
T | G | 105 | a0001c0001t0001g0120a0002c0002t0002g0001a0002c0002t0002g0007others(102): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.-21-8727A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972915 | ||||||
| chr12:45972917
|
T | G | 7 | a0001c0001t0003g0003a0001c0001t0003g0173a0001c0001t0003g0204others(4): Show | 9 | HG00673.hp2 HG01346.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-8729A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972917 | ||||||
| chr12:45972919
|
TAGATATA others(3): Show |
T | 3 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-21-8741_-21-8732d others(12): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972919 | ||||||
| chr12:45972920
|
A | C | 109 | a0001c0001t0001g0120a0001c0029t0003g0130a0002c0002t0002g0001others(106): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-21-8732T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972920 | ||||||
| chr12:45972921
|
G | T | 4 | a0001c0001t0003g0003a0001c0001t0003g0173a0001c0001t0003g0204others(1): Show | 6 | HG00673.hp2 HG01346.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-8733C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972921 | ||||||
| chr12:45972923
|
TATATAGA others(9): Show |
T | 1 | a0009c0014t0003g0024 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-21-8751_-21-8736d others(18): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972923 | ||||||
| chr12:45972927
|
T | TATATAGA others(31): Show |
3 | a0001c0004t0003g0129a0001c0004t0003g0270a0001c0004t0003g0271 | 3 | HG02630.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-21-8740_-21-8739i others(40): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972927 | ||||||
| chr12:45972929
|
G | GAT | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-8743_-21-8742d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972929 | ||||||
| chr12:45972929
|
G | T | 24 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(21): Show | 29 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.-21-8741C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972929 | ||||||
| chr12:45972931
|
T | G | 3 | a0001c0004t0003g0289a0001c0007t0003g0022a0001c0007t0003g0293 | 4 | HG01167.hp2 HG01169.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-8743A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972931 | ||||||
| chr12:45972931
|
T | TAG | 20 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(17): Show | 25 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-21-8744_-21-8743i others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972931 | ||||||
| chr12:45972931
|
T | TATATATA others(3): Show |
36 | a0001c0001t0001g0240a0001c0001t0003g0274a0001c0001t0010g0309others(33): Show | 38 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-21-8744_-21-8743i others(12): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972931 | ||||||
| chr12:45972931
|
TATATATA others(13): Show |
T | 1 | a0001c0001t0003g0201 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-21-8763_-21-8744d others(22): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972931 | ||||||
| chr12:45972937
|
T | G | 1 | a0001c0001t0010g0310 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-21-8749A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972937 | ||||||
| chr12:45972937
|
TAG | T | 76 | a0001c0001t0001g0120a0002c0002t0002g0001a0002c0002t0002g0007others(73): Show | 84 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-21-8751_-21-8750d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972937 | ||||||
| chr12:45972939
|
G | T | 1 | a0001c0001t0010g0310 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-21-8751C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972939 | ||||||
| chr12:45972943
|
T | G | 76 | a0001c0001t0001g0120a0002c0002t0002g0001a0002c0002t0002g0007others(73): Show | 84 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-21-8755A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972943 | ||||||
| chr12:45972945
|
T | G | 2 | a0001c0001t0001g0248a0001c0001t0010g0310 | 2 | HG01346.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-21-8757A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972945 | ||||||
| chr12:45972945
|
T | TAG | 59 | a0001c0001t0001g0240a0001c0001t0003g0274a0001c0001t0010g0309others(56): Show | 66 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-21-8758_-21-8757i others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972945 | ||||||
| chr12:45972945
|
T | TAGATATA others(3): Show |
1 | a0002c0003t0002g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-21-8758_-21-8757i others(12): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972945 | ||||||
| chr12:45972950
|
A | C | 1 | a0002c0003t0002g0036 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-21-8762T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972950 | ||||||
| chr12:45972961
|
T | TATAGATA others(5): Show |
71 | a0001c0001t0001g0120a0002c0002t0002g0001a0002c0002t0002g0007others(68): Show | 79 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-21-8774_-21-8773i others(14): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972961 | ||||||
| chr12:45972963
|
T | TAG | 4 | a0002c0002t0002g0059a0002c0002t0002g0060a0002c0002t0002g0122others(1): Show | 4 | HG00621.hp1 HG02155.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-8776_-21-8775i others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972963 | ||||||
| chr12:45972963
|
TATATATA others(1): Show |
T | 3 | a0001c0001t0003g0180a0001c0001t0003g0188a0001c0007t0003g0022 | 4 | HG01167.hp2 HG01169.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-8783_-21-8776d others(10): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972963 | ||||||
| chr12:45972971
|
G | GAT | 4 | a0002c0002t0002g0059a0002c0002t0002g0060a0002c0002t0002g0122others(1): Show | 4 | HG00621.hp1 HG02155.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-8785_-21-8784d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972971 | ||||||
| chr12:45972975
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-21-8787A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972975 | ||||||
| chr12:45972977
|
TAGATATA others(3): Show |
T | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-8799_-21-8790d others(12): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972977 | ||||||
| chr12:45972987
|
G | T | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-8799C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972987 | ||||||
| chr12:45972989
|
T | TAGATATA others(139): Show |
5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-8802_-21-8801i others(148): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972989 | ||||||
| chr12:45972993
|
G | T | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-21-8805C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972993 | ||||||
| chr12:45972995
|
T | G | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-21-8807A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45972995 | ||||||
| chr12:45973005
|
TATATATA others(1): Show |
T | 4 | a0001c0001t0003g0003a0001c0001t0003g0173a0001c0001t0003g0204others(1): Show | 6 | HG00673.hp2 HG02602.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-8825_-21-8818d others(10): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45973005 | ||||||
| chr12:45973005
|
TATATATA others(9): Show |
T | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-8833_-21-8818d others(18): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45973005 | ||||||
| chr12:45973009
|
T | G | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-21-8821A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45973009 | ||||||
| chr12:45973013
|
G | T | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-21-8825C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45973013 | ||||||
| chr12:45973029
|
G | GATATAGA others(31): Show |
1 | a0001c0004t0003g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-21-8842_-21-8841i others(40): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45973029 | ||||||
| chr12:45973313
|
T | G | 1 | a0002c0002t0002g0121 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-21-9125A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45973313 | ||||||
| chr12:45973645
|
G | A | 3 | a0001c0007t0003g0022a0001c0007t0003g0293a0001c0007t0003g0294 | 4 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-9457C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45973645 | ||||||
| chr12:45973679
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-21-9491C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45973679 | ||||||
| chr12:45973721
|
C | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0251 | 2 | HG01099.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.-21-9533G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45973721 | ||||||
| chr12:45974087
|
A | G | 1 | a0001c0001t0003g0023 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-21-9899T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974087 | ||||||
| chr12:45974120
|
T | C | 111 | a0001c0001t0003g0274a0001c0001t0010g0309a0001c0001t0010g0310others(108): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-21-9932A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974120 | ||||||
| chr12:45974156
|
G | T | 105 | a0002c0002t0002g0001a0002c0002t0002g0007a0002c0002t0002g0009others(102): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.-21-9968C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974156 | ||||||
| chr12:45974161
|
A | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 117 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-21-9973T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974161 | ||||||
| chr12:45974170
|
C | G | 28 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(25): Show | 34 | HG01109.hp1 HG01175.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.-21-9982G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974170 | ||||||
| chr12:45974226
|
G | T | 1 | a0009c0014t0003g0024 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-21-10038C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974226 | ||||||
| chr12:45974261
|
G | A | 1 | a0003c0005t0004g0025 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-21-10073C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974261 | ||||||
| chr12:45974358
|
C | A | 1 | a0001c0001t0001g0210 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-21-10170G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974358 | ||||||
| chr12:45974411
|
G | A | 1 | a0002c0002t0003g0276 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-21-10223C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974411 | ||||||
| chr12:45974600
|
A | G | 5 | a0001c0007t0003g0022a0001c0007t0003g0293a0001c0007t0003g0294others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-10412T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974600 | ||||||
| chr12:45974649
|
T | C | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-10461A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974649 | ||||||
| chr12:45974658
|
A | G | 3 | a0001c0006t0001g0241a0001c0006t0001g0242a0001c0006t0001g0243 | 3 | NA18951.hp2 NA18969.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-21-10470T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974658 | ||||||
| chr12:45974673
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-21-10485G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974673 | ||||||
| chr12:45974896
|
G | A | 5 | a0001c0001t0003g0178a0001c0001t0003g0185a0001c0001t0003g0194others(2): Show | 5 | HG00639.hp2 HG01081.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-10708C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974896 | ||||||
| chr12:45974929
|
T | C | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-21-10741A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45974929 | ||||||
| chr12:45975133
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0166 | 2 | NA18950.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.-21-10945G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45975133 | ||||||
| chr12:45975295
|
C | A | 3 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-21-11107G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45975295 | ||||||
| chr12:45975454
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-21-11266G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45975454 | ||||||
| chr12:45975474
|
C | T | 1 | a0002c0002t0003g0276 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-21-11286G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45975474 | ||||||
| chr12:45975530
|
C | A | 1 | a0002c0002t0002g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-21-11342G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45975530 | ||||||
| chr12:45975587
|
C | G | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-11399G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45975587 | ||||||
| chr12:45975738
|
T | C | 1 | a0002c0003t0002g0106 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-21-11550A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45975738 | ||||||
| chr12:45975901
|
T | C | 1 | a0002c0003t0002g0098 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-21-11713A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45975901 | ||||||
| chr12:45976230
|
A | T | 1 | a0002c0002t0002g0082 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-21-12042T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45976230 | ||||||
| chr12:45976284
|
G | A | 104 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(101): Show | 112 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.-21-12096C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45976284 | ||||||
| chr12:45976333
|
C | G | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(264): Show | 292 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-21-12145G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45976333 | ||||||
| chr12:45976490
|
T | C | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-12302A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45976490 | ||||||
| chr12:45976644
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-21-12456G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45976644 | ||||||
| chr12:45976841
|
G | C | 1 | a0001c0001t0010g0310 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-21-12653C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45976841 | ||||||
| chr12:45976853
|
A | G | 4 | a0002c0002t0002g0045a0002c0002t0002g0057a0002c0002t0002g0058others(1): Show | 4 | NA18979.hp2 NA19057.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-12665T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45976853 | ||||||
| chr12:45976972
|
T | C | 1 | a0002c0003t0002g0126 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-21-12784A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45976972 | ||||||
| chr12:45977019
|
A | T | 2 | a0001c0001t0010g0309a0001c0001t0010g0310 | 2 | HG01346.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-21-12831T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45977019 | ||||||
| chr12:45977028
|
C | T | 1 | a0003c0005t0004g0025 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-21-12840G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45977028 | ||||||
| chr12:45977441
|
A | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0155 | 2 | HG02074.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-22+12912T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45977441 | ||||||
| chr12:45977644
|
T | G | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-22+12709A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45977644 | ||||||
| chr12:45977744
|
T | C | 1 | a0001c0001t0003g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-22+12609A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45977744 | ||||||
| chr12:45977761
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-22+12592G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45977761 | ||||||
| chr12:45977808
|
T | A | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+12545A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45977808 | ||||||
| chr12:45978050
|
C | T | 4 | a0001c0001t0003g0274a0001c0001t0010g0309a0001c0001t0010g0310others(1): Show | 4 | HG01346.hp1 HG02809.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+12303G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45978050 | ||||||
| chr12:45978150
|
C | T | 10 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(7): Show | 10 | HG02451.hp2 HG02647.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22+12203G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45978150 | ||||||
| chr12:45978181
|
A | G | 1 | a0002c0003t0002g0092 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-22+12172T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45978181 | ||||||
| chr12:45978332
|
T | C | 1 | a0002c0002t0002g0034 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-22+12021A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45978332 | ||||||
| chr12:45978377
|
A | T | 3 | a0001c0006t0001g0222a0001c0006t0001g0223a0001c0006t0001g0264 | 3 | HG01167.hp1 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-22+11976T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45978377 | ||||||
| chr12:45978599
|
T | A | 1 | a0001c0001t0001g0163 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-22+11754A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45978599 | ||||||
| chr12:45978634
|
T | C | 23 | a0001c0001t0001g0014a0001c0001t0001g0120a0001c0001t0001g0140others(20): Show | 24 | HG01109.hp2 HG01496.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.-22+11719A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45978634 | ||||||
| chr12:45978843
|
A | C | 2 | a0001c0001t0010g0309a0001c0001t0010g0310 | 2 | HG01346.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-22+11510T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45978843 | ||||||
| chr12:45978897
|
AAAAC | A | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+11452_-22+1145 others(8): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45978897 | ||||||
| chr12:45979057
|
G | A | 1 | a0002c0002t0003g0276 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-22+11296C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45979057 | ||||||
| chr12:45979107
|
A | AG | 311 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(308): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-22+11245dupC | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45979107 | ||||||
| chr12:45979236
|
C | G | 1 | a0002c0002t0003g0276 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-22+11117G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45979236 | ||||||
| chr12:45979300
|
C | A | 1 | a0017c0020t0002g0035 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22+11053G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45979300 | ||||||
| chr12:45979619
|
C | T | 3 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-22+10734G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45979619 | ||||||
| chr12:45979887
|
T | A | 1 | a0001c0001t0003g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-22+10466A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45979887 | ||||||
| chr12:45979888
|
TA | T | 27 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(24): Show | 33 | HG01109.hp1 HG01175.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.-22+10464delT | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45979888 | ||||||
| chr12:45979931
|
G | C | 1 | a0002c0002t0003g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-22+10422C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45979931 | ||||||
| chr12:45980046
|
C | T | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-22+10307G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45980046 | ||||||
| chr12:45980123
|
TG | T | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+10229delC | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45980123 | ||||||
| chr12:45980231
|
A | G | 2 | a0001c0001t0010g0309a0001c0001t0010g0310 | 2 | HG01346.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-22+10122T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45980231 | ||||||
| chr12:45980322
|
G | A | 1 | a0001c0007t0003g0294 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-22+10031C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45980322 | ||||||
| chr12:45980429
|
T | C | 1 | a0001c0001t0013g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-22+9924A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45980429 | ||||||
| chr12:45980624
|
G | C | 1 | a0001c0001t0001g0257 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-22+9729C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45980624 | ||||||
| chr12:45980686
|
T | C | 4 | a0001c0001t0001g0142a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG02074.hp2 HG02523.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+9667A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45980686 | ||||||
| chr12:45980782
|
C | T | 1 | a0005c0009t0001g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-22+9571G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45980782 | ||||||
| chr12:45981005
|
T | A | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+9348A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45981005 | ||||||
| chr12:45981009
|
T | C | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-22+9344A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45981009 | ||||||
| chr12:45981140
|
T | A | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+9213A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45981140 | ||||||
| chr12:45981269
|
T | C | 1 | a0001c0001t0003g0186 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-22+9084A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45981269 | ||||||
| chr12:45981498
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-22+8855G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45981498 | ||||||
| chr12:45981515
|
A | G | 1 | a0001c0001t0003g0187 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-22+8838T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45981515 | ||||||
| chr12:45981523
|
A | G | 106 | a0001c0001t0001g0120a0002c0002t0002g0001a0002c0002t0002g0007others(103): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-22+8830T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45981523 | ||||||
| chr12:45981559
|
G | A | 3 | a0002c0002t0002g0055a0002c0002t0002g0079a0002c0002t0002g0123 | 3 | HG00597.hp1 HG00621.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.-22+8794C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45981559 | ||||||
| chr12:45981618
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-22+8735A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45981618 | ||||||
| chr12:45981654
|
G | A | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+8699C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45981654 | ||||||
| chr12:45981877
|
C | G | 1 | a0002c0003t0018g0037 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-22+8476G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45981877 | ||||||
| chr12:45981924
|
A | G | 2 | a0004c0008t0005g0046a0004c0008t0005g0056 | 2 | HG01071.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-22+8429T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45981924 | ||||||
| chr12:45982067
|
A | C | 3 | a0001c0007t0003g0022a0001c0007t0003g0293a0001c0007t0003g0294 | 4 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+8286T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45982067 | ||||||
| chr12:45982618
|
T | C | 1 | a0002c0002t0002g0034 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-22+7735A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45982618 | ||||||
| chr12:45982908
|
G | A | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+7445C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45982908 | ||||||
| chr12:45982985
|
T | A | 1 | a0001c0001t0001g0239 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-22+7368A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45982985 | ||||||
| chr12:45983147
|
T | C | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+7206A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983147 | ||||||
| chr12:45983150
|
C | T | 2 | a0001c0004t0009g0282a0001c0004t0009g0283 | 2 | HG01175.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-22+7203G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983150 | ||||||
| chr12:45983480
|
C | T | 1 | a0006c0011t0002g0008 | 2 | HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-22+6873G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983480 | ||||||
| chr12:45983742
|
A | AAC | 30 | a0001c0001t0001g0166a0001c0001t0001g0211a0001c0001t0001g0212others(27): Show | 31 | HG00609.hp1 HG00738.hp2 HG02257.hp2 others(28): Show |
intron_variant | MODIFIER | c.-22+6609_-22+6610d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983742 | ||||||
| chr12:45983742
|
A | AACAC | 39 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0164others(36): Show | 42 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-22+6607_-22+6610d others(6): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983742 | ||||||
| chr12:45983742
|
A | AACACAC | 98 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0131others(95): Show | 110 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-22+6605_-22+6610d others(8): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983742 | ||||||
| chr12:45983742
|
A | AACACACA others(1): Show |
68 | a0001c0001t0001g0006a0001c0001t0001g0120a0001c0001t0001g0150others(65): Show | 75 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-22+6603_-22+6610d others(10): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983742 | ||||||
| chr12:45983742
|
A | AACACACA others(3): Show |
23 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0144others(20): Show | 25 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.-22+6601_-22+6610d others(12): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983742 | ||||||
| chr12:45983742
|
A | AACACACA others(5): Show |
9 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(6): Show | 9 | HG00099.hp2 HG02074.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22+6599_-22+6610d others(14): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983742 | ||||||
| chr12:45983742
|
A | AACACACA others(9): Show |
1 | a0001c0001t0001g0214 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-22+6595_-22+6610d others(18): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983742 | ||||||
| chr12:45983742
|
A | C | 1 | a0002c0002t0002g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-22+6611T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983742 | ||||||
| chr12:45983742
|
AAC | A | 14 | a0001c0001t0003g0200a0001c0001t0010g0309a0001c0004t0003g0002others(11): Show | 18 | HG01109.hp1 HG01175.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.-22+6609_-22+6610d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983742 | ||||||
| chr12:45983742
|
AACAC | A | 4 | a0001c0001t0003g0201a0001c0001t0010g0310a0001c0004t0003g0021others(1): Show | 5 | HG00544.hp1 HG01346.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+6607_-22+6610d others(6): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983742 | ||||||
| chr12:45983742
|
AACACACA others(3): Show |
A | 3 | a0001c0007t0003g0022a0001c0007t0003g0293a0001c0007t0003g0294 | 4 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+6601_-22+6610d others(12): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983742 | ||||||
| chr12:45983966
|
A | G | 1 | a0001c0001t0003g0023 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-22+6387T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983966 | ||||||
| chr12:45983990
|
G | A | 6 | a0001c0001t0003g0004a0001c0001t0003g0202a0001c0001t0003g0203others(3): Show | 8 | HG00642.hp1 HG01074.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.-22+6363C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45983990 | ||||||
| chr12:45984019
|
A | G | 5 | a0002c0002t0002g0038a0002c0002t0002g0042a0002c0002t0002g0043others(2): Show | 5 | HG00280.hp2 HG01993.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+6334T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45984019 | ||||||
| chr12:45984023
|
G | C | 32 | a0001c0001t0001g0120a0002c0003t0002g0012a0002c0003t0002g0013others(29): Show | 34 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.-22+6330C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45984023 | ||||||
| chr12:45984114
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-22+6239A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45984114 | ||||||
| chr12:45984158
|
G | A | 108 | a0001c0001t0001g0120a0002c0002t0002g0001a0002c0002t0002g0007others(105): Show | 118 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-22+6195C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45984158 | ||||||
| chr12:45984532
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-22+5821A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45984532 | ||||||
| chr12:45984695
|
C | CT | 38 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(35): Show | 43 | HG00280.hp2 HG01175.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.-22+5657dupA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45984695 | ||||||
| chr12:45984695
|
CT | C | 6 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+5657delA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45984695 | ||||||
| chr12:45984717
|
T | C | 1 | a0002c0002t0002g0113 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-22+5636A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45984717 | ||||||
| chr12:45984783
|
C | G | 1 | a0002c0002t0002g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-22+5570G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45984783 | ||||||
| chr12:45985005
|
T | G | 2 | a0001c0004t0003g0288a0001c0004t0003g0289 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-22+5348A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45985005 | ||||||
| chr12:45985297
|
T | C | 1 | a0002c0003t0002g0013 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-22+5056A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45985297 | ||||||
| chr12:45985537
|
C | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0173a0001c0001t0003g0204 | 5 | HG00673.hp2 NA18962.hp2 NA19070.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+4816G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45985537 | ||||||
| chr12:45985637
|
C | T | 1 | a0002c0003t0018g0037 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-22+4716G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45985637 | ||||||
| chr12:45985650
|
T | A | 4 | a0001c0001t0003g0169a0001c0001t0003g0170a0001c0001t0003g0171others(1): Show | 4 | HG01891.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+4703A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45985650 | ||||||
| chr12:45986086
|
CT | C | 5 | a0003c0005t0004g0025a0003c0005t0004g0026a0003c0005t0004g0027others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+4266delA | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45986086 | ||||||
| chr12:45986378
|
A | G | 268 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(265): Show | 294 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.-22+3975T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45986378 | ||||||
| chr12:45986613
|
G | T | 1 | a0014c0022t0001g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-22+3740C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45986613 | ||||||
| chr12:45986615
|
T | G | 1 | a0014c0022t0001g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-22+3738A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45986615 | ||||||
| chr12:45986616
|
A | T | 1 | a0014c0022t0001g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-22+3737T>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45986616 | ||||||
| chr12:45986619
|
C | T | 1 | a0014c0022t0001g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-22+3734G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45986619 | ||||||
| chr12:45986756
|
G | A | 1 | a0001c0006t0001g0264 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-22+3597C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45986756 | ||||||
| chr12:45986803
|
G | A | 1 | a0001c0001t0003g0204 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-22+3550C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45986803 | ||||||
| chr12:45986842
|
T | C | 1 | a0001c0001t0001g0265 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-22+3511A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45986842 | ||||||
| chr12:45986856
|
C | T | 1 | a0003c0005t0004g0025 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-22+3497G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45986856 | ||||||
| chr12:45986934
|
A | C | 1 | a0001c0004t0003g0277 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-22+3419T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45986934 | ||||||
| chr12:45987423
|
C | T | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(264): Show | 292 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-22+2930G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45987423 | ||||||
| chr12:45987448
|
G | C | 1 | a0002c0002t0002g0114 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-22+2905C>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45987448 | ||||||
| chr12:45987462
|
C | A | 1 | a0001c0001t0013g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-22+2891G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45987462 | ||||||
| chr12:45987482
|
G | T | 23 | a0001c0004t0003g0002a0001c0004t0003g0020a0001c0004t0003g0021others(20): Show | 28 | HG01175.hp2 HG01884.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-22+2871C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45987482 | ||||||
| chr12:45987644
|
C | T | 5 | a0001c0004t0003g0129a0001c0004t0003g0270a0001c0004t0003g0271others(2): Show | 5 | HG02630.hp1 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+2709G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45987644 | ||||||
| chr12:45987729
|
T | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0266a0001c0001t0001g0267others(2): Show | 6 | HG02258.hp2 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+2624A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45987729 | ||||||
| chr12:45987800
|
T | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 117 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-22+2553A>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45987800 | ||||||
| chr12:45987924
|
TTA | T | 34 | a0001c0001t0001g0014a0001c0001t0001g0140a0001c0001t0001g0141others(31): Show | 35 | HG00438.hp1 HG01109.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.-22+2427_-22+2428d others(4): Show |
SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45987924 | ||||||
| chr12:45987945
|
T | A | 43 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(40): Show | 50 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(47): Show |
intron_variant | MODIFIER | c.-22+2408A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45987945 | ||||||
| chr12:45987955
|
T | A | 3 | a0002c0010t0002g0115a0002c0010t0002g0116a0002c0010t0002g0127 | 3 | NA18947.hp2 NA18970.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-22+2398A>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45987955 | ||||||
| chr12:45987990
|
A | G | 1 | a0002c0019t0003g0296 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-22+2363T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45987990 | ||||||
| chr12:45988182
|
C | A | 1 | a0001c0004t0003g0295 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-22+2171G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45988182 | ||||||
| chr12:45988473
|
C | A | 148 | a0001c0001t0003g0274a0001c0001t0003g0290a0001c0001t0003g0291others(145): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-22+1880G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45988473 | ||||||
| chr12:45989043
|
C | T | 1 | a0017c0020t0002g0035 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22+1310G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45989043 | ||||||
| chr12:45989138
|
A | G | 5 | a0003c0005t0006g0134a0003c0005t0006g0135a0003c0005t0006g0136others(2): Show | 5 | HG02451.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+1215T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45989138 | ||||||
| chr12:45989398
|
A | G | 5 | a0002c0002t0002g0030a0002c0002t0002g0031a0002c0002t0002g0032others(2): Show | 5 | HG02129.hp2 NA18747.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+955T>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45989398 | ||||||
| chr12:45989469
|
G | A | 1 | a0002c0019t0003g0296 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-22+884C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45989469 | ||||||
| chr12:45989699
|
G | A | 3 | a0002c0002t0002g0117a0002c0002t0002g0118a0002c0002t0002g0119 | 3 | HG02486.hp2 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-22+654C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45989699 | ||||||
| chr12:45989790
|
C | T | 1 | a0001c0004t0003g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-22+563G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45989790 | ||||||
| chr12:45989839
|
T | C | 1 | a0001c0001t0003g0023 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-22+514A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45989839 | ||||||
| chr12:45989975
|
T | TC | 16 | a0001c0001t0001g0120a0001c0001t0001g0297a0001c0001t0003g0298others(13): Show | 16 | HG00597.hp1 HG00642.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.-22+377dupG | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45989975 | ||||||
| chr12:45989979
|
C | G | 1 | a0015c0024t0001g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-22+374G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45989979 | ||||||
| chr12:45989983
|
C | A | 1 | a0001c0001t0013g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-22+370G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45989983 | ||||||
| chr12:45989984
|
C | A | 2 | a0001c0007t0008g0306a0001c0007t0008g0307 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-22+369G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45989984 | ||||||
| chr12:45989989
|
A | C | 1 | a0001c0001t0001g0131 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-22+364T>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45989989 | ||||||
| chr12:45990000
|
C | A | 1 | a0001c0001t0003g0308 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-22+353G>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45990000 | ||||||
| chr12:45990010
|
G | T | 1 | a0001c0029t0003g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-22+343C>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45990010 | ||||||
| chr12:45990037
|
G | A | 1 | a0009c0014t0003g0024 | 2 | HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-22+316C>T | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45990037 | ||||||
| chr12:45990168
|
C | G | 1 | a0001c0004t0003g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-22+185G>C | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45990168 | ||||||
| chr12:45990218
|
C | T | 1 | a0002c0002t0003g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-22+135G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45990218 | ||||||
| chr12:45990241
|
C | T | 106 | a0001c0001t0001g0120a0002c0002t0002g0001a0002c0002t0002g0007others(103): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-22+112G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45990241 | ||||||
| chr12:45990247
|
T | C | 106 | a0001c0001t0001g0120a0002c0002t0002g0001a0002c0002t0002g0007others(103): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-22+106A>G | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45990247 | ||||||
| chr12:45990248
|
C | T | 106 | a0001c0001t0001g0120a0002c0002t0002g0001a0002c0002t0002g0007others(103): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-22+105G>A | SCAF11 | ENSG00000139218.18 | transcript | ENST00000369367.8 | protein_coding | 1/14 | chr12 | 45990248 |