Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57466 |
|---|---|
| ensemblid | ENSG00000156304.15 |
| hgncid | 19304 |
| symbol | SCAF4 |
| name | SR-related CTD associated factor 4 |
| refseq_nuc | NM_020706.2 |
| refseq_prot | NP_065757.1 |
| ensembl_nuc | ENST00000286835.12 |
| ensembl_prot | ENSP00000286835.7 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 31671000 |
| end | 31732118 |
| strand | - |
| ver | v1.2 |
| region | chr21:31671000-31732118 |
| region5000 | chr21:31666000-31737118 |
| regionname0 | SCAF4_chr21_31671000_31732118 |
| regionname5000 | SCAF4_chr21_31666000_31737118 |
| 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 | 1147 | 344 | 75 | 72 | 147 | 10 | 38 | 117 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0002 | 0/0 | 1147 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0003 | 0/0 | 1147 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0004 | 0/0 | 1147 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0005 | 0/0 | 1147 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0006 | 0/0 | 1147 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0007 | 0/0 | 1147 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| 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 | 3444 | 269 | 44 | 53 | 130 | 9 | 31 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0002 | 0/0 | 3444 | 42 | 11 | 8 | 15 | 1 | 7 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0003 | 0/0 | 3444 | 13 | 11 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0004 | 0/0 | 3444 | 9 | 7 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0005 | 0/0 | 3444 | 3 | 0 | 3 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0006 | 0/0 | 3444 | 3 | 0 | 2 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0007 | 0/0 | 3444 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0008 | 0/0 | 3444 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0009 | 0/0 | 3444 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0010 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0011 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0012 | 0/0 | 3444 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0013 | 0/0 | 3444 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0014 | 0/0 | 3444 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0015 | 0/0 | 3444 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0016 | 0/0 | 3444 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| c0017 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 826 | 312 | 69 | 61 | 137 | 9 | 34 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| t0002 | 0/0 | 825 | 20 | 5 | 4 | 11 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| t0003 | 0/0 | 822 | 10 | 0 | 5 | 0 | 0 | 5 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| t0004 | 0/0 | 827 | 6 | 0 | 2 | 2 | 1 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| t0005 | 0/0 | 826 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| t0006 | 0/0 | 827 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| t0007 | 0/0 | 826 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| t0008 | 0/0 | 826 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| 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 | 3444 | 269 | 44 | 53 | 130 | 9 | 31 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0002 | 0/0 | 3444 | 42 | 11 | 8 | 15 | 1 | 7 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0003 | 0/0 | 3444 | 13 | 11 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0004 | 0/0 | 3444 | 9 | 7 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0005 | 0/0 | 3444 | 3 | 0 | 3 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0007 | 0/0 | 3444 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0008 | 0/0 | 3444 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0009 | 0/0 | 3444 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0011 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0013 | 0/0 | 3444 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0017 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0002c0006 | 0/0 | 3444 | 3 | 0 | 2 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0003c0010 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0004c0015 | 0/0 | 3444 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0005c0012 | 0/0 | 3444 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0006c0014 | 0/0 | 3444 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0007c0016 | 0/0 | 3444 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4269 | 241 | 42 | 46 | 118 | 8 | 25 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0001t0002 | 0/0 | 4268 | 12 | 1 | 1 | 10 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0001t0003 | 0/0 | 4265 | 10 | 0 | 5 | 0 | 0 | 5 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0001t0004 | 0/0 | 4270 | 5 | 0 | 1 | 2 | 1 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0001t0006 | 0/0 | 4270 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0002t0001 | 0/0 | 4269 | 37 | 10 | 5 | 14 | 1 | 7 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0002t0002 | 0/0 | 4268 | 2 | 1 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0002t0004 | 0/0 | 4270 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0002t0007 | 0/0 | 4269 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0002t0008 | 0/0 | 4269 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0003t0001 | 0/0 | 4269 | 8 | 7 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0003t0002 | 0/0 | 4268 | 4 | 3 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0003t0005 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0004t0001 | 0/0 | 4269 | 9 | 7 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0005t0001 | 0/0 | 4269 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0005t0002 | 0/0 | 4268 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0007t0001 | 0/0 | 4269 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0008t0001 | 0/0 | 4269 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0009t0001 | 0/0 | 4269 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0011t0001 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0013t0001 | 0/0 | 4269 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0001c0017t0001 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0002c0006t0001 | 0/0 | 4269 | 3 | 0 | 2 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0003c0010t0001 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0004c0015t0001 | 0/0 | 4269 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0005c0012t0001 | 0/0 | 4269 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0006c0014t0001 | 0/0 | 4269 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| a0007c0016t0001 | 0/0 | 4269 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | copy fasta | chr21 | 31666000 | 31737118 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0007g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0002t0008g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0003t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0005t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0005t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0005t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0007t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0007t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0008t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0008t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0009t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0011t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0013t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0001c0017t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0002c0006t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0002c0006t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0002c0006t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0003c0010t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0004c0015t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0005c0012t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0006c0014t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| a0007c0016t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | GBR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0338 | EUR | GBR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | GBR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00639 | hp2 | a0001 | c0004 | t0001 | g0190 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00738 | hp1 | a0001 | c0005 | t0002 | g0344 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00741 | hp1 | a0001 | c0008 | t0001 | g0212 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01070 | hp2 | a0001 | c0009 | t0001 | g0144 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01074 | hp2 | a0002 | c0006 | t0001 | g0277 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01099 | hp1 | a0001 | c0005 | t0001 | g0345 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0016 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01106 | hp2 | a0001 | c0008 | t0001 | g0166 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0141 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0011 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01243 | hp2 | a0002 | c0006 | t0001 | g0326 | AMR | PUR | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01261 | hp2 | a0001 | c0005 | t0002 | g0343 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01346 | hp1 | a0001 | c0002 | t0008 | g0347 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0036 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0217 | EUR | IBS | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01891 | hp1 | a0001 | c0003 | t0005 | g0021 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0010 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01934 | hp1 | a0001 | c0013 | t0001 | g0281 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01934 | hp2 | a0001 | c0002 | t0007 | g0346 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0121 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02071 | hp1 | a0006 | c0014 | t0001 | g0113 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02135 | hp2 | a0007 | c0016 | t0001 | g0282 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CDX | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | CDX | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0227 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0001 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | KHV | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0203 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0122 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0123 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0170 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0189 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0143 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0341 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0220 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0124 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0139 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0187 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02970 | hp1 | a0001 | c0011 | t0001 | g0325 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0125 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0331 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0186 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0120 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0118 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0126 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0211 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0327 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03492 | hp2 | a0004 | c0015 | t0001 | g0022 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0188 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0332 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03710 | hp1 | a0002 | c0006 | t0001 | g0308 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0214 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0337 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0333 | SAS | BEB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18974 | hp1 | a0001 | c0007 | t0001 | g0323 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18980 | hp1 | a0001 | c0007 | t0001 | g0293 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0119 | AFR | LWK | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19086 | hp1 | a0005 | c0012 | t0001 | g0044 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | YRI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ASW | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ASW | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0210 | EUR | TSI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0009 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0001 | AFR | ACB | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG03471 | hp2 | a0001 | c0017 | t0001 | g0147 | AFR | MSL | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | USA | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | USA | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | USA | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| NA21309 | hp2 | a0003 | c0010 | t0001 | g0145 | AFR | LWK | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0236 | REF | REF | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0233 | REF | REF | SCAF4_chr21_31666000_31737118 | SCAF4 | chr21 | 31666000 | 31737118 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:31671418
|
G | A | 1 | a0005 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.3425C>T | p.Ala1142Val | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 3851/4269 | 3425/3444 | 1142/1147 | chr21 | 31671418 | ||
| chr21:31671571
|
T | C | 1 | a0006 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.3272A>G | p.Lys1091Arg | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 3698/4269 | 3272/3444 | 1091/1147 | chr21 | 31671571 | ||
| chr21:31693399
|
G | A | 1 | a0004 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.1408C>T | p.Arg470Cys | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 12/20 | 1834/4269 | 1408/3444 | 470/1147 | chr21 | 31693399 | ||
| chr21:31694928
|
G | C | 1 | a0007 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.1121C>G | p.Pro374Arg | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/20 | 1547/4269 | 1121/3444 | 374/1147 | chr21 | 31694928 | ||
| chr21:31696624
|
C | A | 1 | a0002 | 3 | HG01074.hp2 HG01243.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.904G>T | p.Val302Leu | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/20 | 1330/4269 | 904/3444 | 302/1147 | chr21 | 31696624 | ||
| chr21:31696683
|
G | T | 1 | a0003 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.845C>A | p.Thr282Asn | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/20 | 1271/4269 | 845/3444 | 282/1147 | chr21 | 31696683 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:31671507
|
C | A | 1 | a0001c0013 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.3336G>T | p.Gly1112Gly | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 3762/4269 | 3336/3444 | 1112/1147 | chr21 | 31671507 | ||
| chr21:31672065
|
G | A | 1 | a0001c0008 | 2 | HG00741.hp1 HG01106.hp2 |
synonymous_variant | LOW | c.2778C>T | p.Gly926Gly | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 3204/4269 | 2778/3444 | 926/1147 | chr21 | 31672065 | ||
| chr21:31672095
|
A | G | 1 | a0001c0005 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
synonymous_variant | LOW | c.2748T>C | p.Val916Val | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 3174/4269 | 2748/3444 | 916/1147 | chr21 | 31672095 | ||
| chr21:31685432
|
A | C | 1 | a0001c0017 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.2262T>G | p.Pro754Pro | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 18/20 | 2688/4269 | 2262/3444 | 754/1147 | chr21 | 31685432 | ||
| chr21:31685671
|
A | C | 1 | a0001c0011 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.2106T>G | p.Pro702Pro | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 17/20 | 2532/4269 | 2106/3444 | 702/1147 | chr21 | 31685671 | ||
| chr21:31693373
|
A | G | 2 | a0001c0003a0001c0011 | 14 | HG01106.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
synonymous_variant | LOW | c.1434T>C | p.Ser478Ser | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 12/20 | 1860/4269 | 1434/3444 | 478/1147 | chr21 | 31693373 | ||
| chr21:31696649
|
T | C | 4 | a0001c0002a0001c0008a0001c0009others(1): Show | 46 | HG00735.hp2 HG00738.hp2 HG00741.hp1 others(43): Show |
synonymous_variant | LOW | c.879A>G | p.Ala293Ala | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/20 | 1305/4269 | 879/3444 | 293/1147 | chr21 | 31696649 | ||
| chr21:31702320
|
A | G | 2 | a0001c0008a0001c0009 | 3 | HG00741.hp1 HG01070.hp2 HG01106.hp2 |
synonymous_variant | LOW | c.381T>C | p.Ile127Ile | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 5/20 | 807/4269 | 381/3444 | 127/1147 | chr21 | 31702320 | ||
| chr21:31702353
|
A | C | 1 | a0001c0004 | 9 | HG00639.hp2 HG01175.hp2 HG01891.hp2 others(6): Show |
synonymous_variant | LOW | c.348T>G | p.Leu116Leu | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 5/20 | 774/4269 | 348/3444 | 116/1147 | chr21 | 31702353 | ||
| chr21:31703906
|
A | C | 1 | a0001c0007 | 2 | NA18974.hp1 NA18980.hp1 |
synonymous_variant | LOW | c.180T>G | p.Val60Val | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/20 | 606/4269 | 180/3444 | 60/1147 | chr21 | 31703906 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:31671108
|
T | TA | 3 | a0001c0001t0004a0001c0001t0006a0001c0002t0004 | 7 | HG01109.hp2 HG01361.hp2 HG01515.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*290dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 290 | chr21 | 31671108 | |||||
| chr21:31671108
|
TA | T | 4 | a0001c0001t0002a0001c0002t0002a0001c0003t0002others(1): Show | 20 | HG00738.hp1 HG01106.hp1 HG01261.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*290delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 290 | chr21 | 31671108 | |||||
| chr21:31671126
|
TAGAG | T | 1 | a0001c0001t0003 | 10 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*269_*272delCTCT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 269 | chr21 | 31671126 | |||||
| chr21:31671130
|
G | A | 1 | a0001c0003t0005 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*269C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 269 | chr21 | 31671130 | |||||
| chr21:31671366
|
G | A | 1 | a0001c0001t0006 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*33C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 20/20 | 33 | chr21 | 31671366 | |||||
| chr21:31732035
|
G | C | 1 | a0001c0002t0007 | 1 | HG01934.hp2 | 5_prime_UTR_variant | MODIFIER | c.-343C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/20 | 343 | chr21 | 31732035 | |||||
| chr21:31732115
|
C | A | 1 | a0001c0002t0008 | 1 | HG01346.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-423G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/20 | chr21 | 31732115 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:31672507
|
A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(101): Show | 105 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.2489-153T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31672507 | ||||||
| chr21:31672943
|
G | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2489-589C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31672943 | ||||||
| chr21:31672945
|
T | C | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2489-591A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31672945 | ||||||
| chr21:31673251
|
T | C | 1 | a0001c0001t0004g0192 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2489-897A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673251 | ||||||
| chr21:31673403
|
G | C | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2489-1049C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673403 | ||||||
| chr21:31673471
|
A | ATACTTTA others(672): Show |
6 | a0001c0003t0002g0001a0001c0003t0002g0016a0001c0005t0001g0345others(3): Show | 7 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.2489-1118_2489-111 others(683): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673471 | ||||||
| chr21:31673471
|
A | ATACTTTA others(672): Show |
5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2489-1118_2489-111 others(683): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673471 | ||||||
| chr21:31673520
|
G | A | 5 | a0001c0001t0001g0255a0001c0002t0001g0155a0001c0002t0001g0164others(2): Show | 5 | HG02523.hp2 NA18947.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.2489-1166C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673520 | ||||||
| chr21:31673842
|
C | T | 1 | a0001c0003t0002g0001 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2489-1488G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673842 | ||||||
| chr21:31673903
|
TA | T | 6 | a0001c0003t0002g0001a0001c0003t0002g0016a0001c0005t0001g0345others(3): Show | 7 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.2489-1550delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673903 | ||||||
| chr21:31673921
|
A | C | 343 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(340): Show | 348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.2489-1567T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673921 | ||||||
| chr21:31673970
|
T | A | 326 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.2489-1616A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673970 | ||||||
| chr21:31673987
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076 | 3 | HG02622.hp2 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2489-1633C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31673987 | ||||||
| chr21:31674208
|
A | C | 12 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.2489-1854T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674208 | ||||||
| chr21:31674404
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2489-2050G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674404 | ||||||
| chr21:31674681
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2489-2327G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674681 | ||||||
| chr21:31674692
|
T | C | 9 | a0001c0001t0001g0245a0001c0001t0001g0259a0001c0001t0001g0272others(6): Show | 9 | HG02015.hp1 HG02165.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.2489-2338A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674692 | ||||||
| chr21:31674751
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2489-2397C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674751 | ||||||
| chr21:31674786
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0222 | 2 | HG01081.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.2489-2432A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674786 | ||||||
| chr21:31674822
|
A | AT | 3 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340 | 3 | HG00099.hp2 HG01433.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2489-2469dupA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674822 | ||||||
| chr21:31674851
|
T | C | 1 | a0001c0001t0001g0258 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2489-2497A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674851 | ||||||
| chr21:31674875
|
G | T | 1 | a0001c0001t0003g0163 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2489-2521C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31674875 | ||||||
| chr21:31675004
|
T | C | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2489-2650A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675004 | ||||||
| chr21:31675005
|
T | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(94): Show | 98 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2489-2651A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675005 | ||||||
| chr21:31675046
|
A | C | 1 | a0001c0001t0001g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2489-2692T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675046 | ||||||
| chr21:31675067
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2489-2713A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675067 | ||||||
| chr21:31675234
|
A | G | 2 | a0001c0001t0003g0007a0001c0001t0003g0008 | 2 | HG00639.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2489-2880T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675234 | ||||||
| chr21:31675235
|
T | C | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2489-2881A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675235 | ||||||
| chr21:31675508
|
T | A | 326 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.2489-3154A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675508 | ||||||
| chr21:31675645
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2489-3291C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675645 | ||||||
| chr21:31675702
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2489-3348C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675702 | ||||||
| chr21:31675828
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2489-3474T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675828 | ||||||
| chr21:31675883
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2489-3529G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675883 | ||||||
| chr21:31675909
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0225 | 4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2489-3555C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675909 | ||||||
| chr21:31675919
|
T | C | 2 | a0001c0001t0001g0171a0001c0003t0002g0126 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2489-3565A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675919 | ||||||
| chr21:31675922
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2489-3568C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675922 | ||||||
| chr21:31675948
|
C | T | 3 | a0001c0001t0001g0251a0001c0008t0001g0166a0001c0008t0001g0212 | 3 | HG00140.hp1 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2489-3594G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31675948 | ||||||
| chr21:31676003
|
T | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(9): Show | 13 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2489-3649A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676003 | ||||||
| chr21:31676044
|
A | C | 1 | a0001c0003t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2489-3690T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676044 | ||||||
| chr21:31676100
|
G | C | 9 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(6): Show | 9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2489-3746C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676100 | ||||||
| chr21:31676230
|
G | A | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2489-3876C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676230 | ||||||
| chr21:31676493
|
G | C | 1 | a0001c0008t0001g0212 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2489-4139C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676493 | ||||||
| chr21:31676551
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.2489-4197A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676551 | ||||||
| chr21:31676592
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2489-4238G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676592 | ||||||
| chr21:31676865
|
ATCTG | A | 9 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(6): Show | 9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2489-4515_2489-451 others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676865 | ||||||
| chr21:31676940
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2489-4586C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31676940 | ||||||
| chr21:31677077
|
C | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(5): Show | 9 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2489-4723G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677077 | ||||||
| chr21:31677154
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2489-4800G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677154 | ||||||
| chr21:31677404
|
T | C | 1 | a0001c0002t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2489-5050A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677404 | ||||||
| chr21:31677476
|
C | T | 4 | a0001c0002t0001g0012a0001c0002t0001g0203a0001c0002t0001g0210others(1): Show | 4 | HG02602.hp1 HG03704.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2489-5122G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677476 | ||||||
| chr21:31677579
|
A | C | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0239 | 3 | HG03491.hp1 HG03492.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2489-5225T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677579 | ||||||
| chr21:31677649
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2489-5295G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677649 | ||||||
| chr21:31677677
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2489-5323G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677677 | ||||||
| chr21:31677803
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2489-5449A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677803 | ||||||
| chr21:31677816
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2489-5462G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677816 | ||||||
| chr21:31677826
|
T | C | 1 | a0001c0008t0001g0166 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2489-5472A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677826 | ||||||
| chr21:31677972
|
T | TACCTTAG others(4): Show |
1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2489-5629_2489-561 others(15): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677972 | ||||||
| chr21:31677974
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0004g0279 | 2 | NA18967.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.2489-5620G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31677974 | ||||||
| chr21:31678005
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2489-5651G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678005 | ||||||
| chr21:31678162
|
T | C | 3 | a0001c0003t0002g0001a0001c0003t0002g0016a0001c0011t0001g0325 | 4 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489-5808A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678162 | ||||||
| chr21:31678264
|
A | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0087 | 2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2489-5910T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678264 | ||||||
| chr21:31678390
|
A | G | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2489-6036T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678390 | ||||||
| chr21:31678406
|
C | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0218 | 2 | HG01074.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2489-6052G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678406 | ||||||
| chr21:31678472
|
T | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(94): Show | 98 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2489-6118A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678472 | ||||||
| chr21:31678520
|
T | TAAAAACT others(318): Show |
3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2489-6167_2489-616 others(329): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678520 | ||||||
| chr21:31678621
|
T | C | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2489-6267A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31678621 | ||||||
| chr21:31679098
|
G | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2488+5951C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31679098 | ||||||
| chr21:31679211
|
T | C | 91 | a0001c0001t0001g0090a0001c0001t0001g0112a0001c0001t0001g0117others(88): Show | 91 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2488+5838A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31679211 | ||||||
| chr21:31679338
|
GGTTT | G | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2488+5707_2488+571 others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31679338 | ||||||
| chr21:31679502
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(97): Show | 101 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2488+5547A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31679502 | ||||||
| chr21:31679683
|
GAT | G | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2488+5364_2488+536 others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31679683 | ||||||
| chr21:31680385
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2488+4664A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31680385 | ||||||
| chr21:31680834
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2488+4215A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31680834 | ||||||
| chr21:31680915
|
C | T | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2488+4134G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31680915 | ||||||
| chr21:31681328
|
C | A | 1 | a0001c0001t0001g0098 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2488+3721G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681328 | ||||||
| chr21:31681547
|
T | C | 111 | a0001c0001t0001g0005a0001c0001t0001g0090a0001c0001t0001g0117others(108): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.2488+3502A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681547 | ||||||
| chr21:31681567
|
G | A | 111 | a0001c0001t0001g0005a0001c0001t0001g0090a0001c0001t0001g0117others(108): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.2488+3482C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681567 | ||||||
| chr21:31681674
|
T | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(94): Show | 98 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2488+3375A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681674 | ||||||
| chr21:31681762
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2488+3287A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681762 | ||||||
| chr21:31681796
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2488+3253C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681796 | ||||||
| chr21:31681994
|
T | C | 3 | a0001c0003t0002g0001a0001c0003t0002g0016a0001c0011t0001g0325 | 4 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+3055A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31681994 | ||||||
| chr21:31682103
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2488+2946A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682103 | ||||||
| chr21:31682213
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2488+2836A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682213 | ||||||
| chr21:31682214
|
A | G | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG00423.hp2 HG02074.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.2488+2835T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682214 | ||||||
| chr21:31682231
|
C | T | 19 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(16): Show | 21 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.2488+2818G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682231 | ||||||
| chr21:31682250
|
G | A | 3 | a0001c0003t0002g0001a0001c0003t0002g0016a0001c0011t0001g0325 | 4 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+2799C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682250 | ||||||
| chr21:31682251
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2488+2798G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682251 | ||||||
| chr21:31682313
|
A | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0225 | 4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2488+2736T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682313 | ||||||
| chr21:31682376
|
C | CA | 98 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(95): Show | 100 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2488+2672dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682376 | ||||||
| chr21:31682414
|
A | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(5): Show | 9 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2488+2635T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682414 | ||||||
| chr21:31682448
|
G | A | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(233): Show | 240 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2488+2601C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682448 | ||||||
| chr21:31682551
|
C | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(5): Show | 9 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2488+2498G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682551 | ||||||
| chr21:31682812
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2488+2237G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682812 | ||||||
| chr21:31682822
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2488+2227C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682822 | ||||||
| chr21:31682900
|
T | G | 1 | a0001c0001t0001g0341 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2488+2149A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31682900 | ||||||
| chr21:31683120
|
C | T | 3 | a0001c0003t0002g0001a0001c0003t0002g0016a0001c0011t0001g0325 | 4 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+1929G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683120 | ||||||
| chr21:31683342
|
C | T | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2488+1707G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683342 | ||||||
| chr21:31683444
|
A | C | 4 | a0001c0001t0001g0104a0001c0001t0002g0103a0001c0001t0006g0017others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+1605T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683444 | ||||||
| chr21:31683467
|
C | T | 1 | a0001c0002t0001g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2488+1582G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683467 | ||||||
| chr21:31683628
|
C | A | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2488+1421G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683628 | ||||||
| chr21:31683668
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076 | 3 | HG02622.hp2 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2488+1381C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683668 | ||||||
| chr21:31683709
|
G | GA | 10 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(7): Show | 10 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2488+1339dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31683709 | ||||||
| chr21:31684027
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2488+1022A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684027 | ||||||
| chr21:31684152
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2488+897T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684152 | ||||||
| chr21:31684260
|
G | A | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(234): Show | 241 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.2488+789C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684260 | ||||||
| chr21:31684374
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2488+675T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684374 | ||||||
| chr21:31684423
|
C | A | 20 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(17): Show | 20 | HG00140.hp2 HG01099.hp2 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.2488+626G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684423 | ||||||
| chr21:31684499
|
T | C | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2488+550A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684499 | ||||||
| chr21:31684523
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2488+526C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684523 | ||||||
| chr21:31684546
|
G | A | 4 | a0001c0001t0001g0104a0001c0001t0002g0103a0001c0001t0006g0017others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+503C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684546 | ||||||
| chr21:31684616
|
G | T | 1 | a0001c0002t0001g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2488+433C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684616 | ||||||
| chr21:31684617
|
T | G | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2488+432A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684617 | ||||||
| chr21:31684850
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2488+199A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684850 | ||||||
| chr21:31684981
|
T | C | 5 | a0001c0001t0001g0263a0001c0001t0001g0295a0001c0001t0001g0299others(2): Show | 5 | NA18943.hp2 NA18946.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.2488+68A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684981 | ||||||
| chr21:31684999
|
T | G | 3 | a0001c0001t0001g0049a0001c0001t0001g0248a0001c0008t0001g0212 | 3 | HG00741.hp1 HG03831.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2488+50A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684999 | ||||||
| chr21:31684999
|
TG | T | 254 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(251): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.2488+49delC | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31684999 | ||||||
| chr21:31685000
|
G | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0248a0001c0008t0001g0212 | 3 | HG00741.hp1 HG03831.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2488+49C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31685000 | ||||||
| chr21:31685001
|
G | A | 1 | a0001c0003t0002g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2488+48C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31685001 | ||||||
| chr21:31685003
|
G | C | 2 | a0001c0001t0001g0284a0001c0001t0002g0286 | 2 | NA18955.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2488+46C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31685003 | ||||||
| chr21:31685014
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2488+35C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 19/19 | chr21 | 31685014 | ||||||
| chr21:31685495
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2210-11T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 17/19 | chr21 | 31685495 | ||||||
| chr21:31685529
|
C | T | 1 | a0001c0007t0001g0293 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2209+39G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 17/19 | chr21 | 31685529 | ||||||
| chr21:31685539
|
A | G | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2209+29T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 17/19 | chr21 | 31685539 | ||||||
| chr21:31685547
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2209+21A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 17/19 | chr21 | 31685547 | ||||||
| chr21:31685762
|
C | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0170a0001c0002t0001g0226 | 3 | HG01109.hp1 HG02683.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2044-29G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31685762 | ||||||
| chr21:31685863
|
T | C | 7 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(4): Show | 7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-130A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31685863 | ||||||
| chr21:31686151
|
C | T | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2044-418G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686151 | ||||||
| chr21:31686203
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2044-485_2044-471d others(17): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686203 | ||||||
| chr21:31686214
|
AAAG | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(5): Show | 10 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2044-484_2044-482d others(5): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686214 | ||||||
| chr21:31686215
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(106): Show | 110 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.2044-482T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686215 | ||||||
| chr21:31686216
|
AG | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(101): Show | 105 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.2044-484delC | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686216 | ||||||
| chr21:31686217
|
G | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0053others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-484C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686217 | ||||||
| chr21:31686217
|
GA | G | 6 | a0001c0001t0001g0178a0001c0001t0001g0251a0001c0001t0001g0262others(3): Show | 6 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2044-485delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686217 | ||||||
| chr21:31686218
|
A | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(5): Show | 10 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2044-485T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686218 | ||||||
| chr21:31686231
|
A | G | 4 | a0001c0001t0001g0104a0001c0001t0002g0103a0001c0001t0006g0017others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2044-498T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686231 | ||||||
| chr21:31686258
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(8): Show | 13 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.2044-525G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686258 | ||||||
| chr21:31686364
|
C | T | 343 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(340): Show | 348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.2044-631G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686364 | ||||||
| chr21:31686407
|
A | G | 6 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(3): Show | 6 | HG01952.hp2 HG02622.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2044-674T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686407 | ||||||
| chr21:31686430
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(117): Show | 123 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.2044-697G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686430 | ||||||
| chr21:31686566
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2044-833C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686566 | ||||||
| chr21:31686669
|
C | T | 1 | a0001c0003t0002g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2044-936G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686669 | ||||||
| chr21:31686735
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(236): Show | 243 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.2044-1002T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686735 | ||||||
| chr21:31686853
|
T | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(8): Show | 13 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.2044-1120A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686853 | ||||||
| chr21:31686920
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2044-1187G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31686920 | ||||||
| chr21:31687160
|
C | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2043+1147G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687160 | ||||||
| chr21:31687184
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0002g0103a0001c0001t0006g0017 | 3 | HG03098.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2043+1123G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687184 | ||||||
| chr21:31687230
|
A | C | 3 | a0001c0003t0002g0001a0001c0003t0002g0016a0001c0011t0001g0325 | 4 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2043+1077T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687230 | ||||||
| chr21:31687259
|
G | A | 1 | a0002c0006t0001g0277 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2043+1048C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687259 | ||||||
| chr21:31687276
|
C | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(118): Show | 124 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.2043+1031G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687276 | ||||||
| chr21:31687316
|
T | C | 1 | a0001c0003t0002g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2043+991A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687316 | ||||||
| chr21:31687518
|
T | C | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2043+789A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687518 | ||||||
| chr21:31687701
|
CA | C | 46 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(43): Show | 46 | HG00735.hp2 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.2043+605delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687701 | ||||||
| chr21:31687716
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2043+591T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687716 | ||||||
| chr21:31687836
|
G | A | 7 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(4): Show | 7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2043+471C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687836 | ||||||
| chr21:31687873
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2043+434G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31687873 | ||||||
| chr21:31688060
|
T | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076 | 3 | HG02622.hp2 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2043+247A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688060 | ||||||
| chr21:31688114
|
C | CA | 81 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0090others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2043+192dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAA | 68 | a0001c0001t0001g0112a0001c0001t0001g0131a0001c0001t0001g0132others(65): Show | 68 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2043+191_2043+192d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAA | 35 | a0001c0001t0001g0136a0001c0001t0001g0154a0001c0001t0001g0156others(32): Show | 35 | HG00423.hp2 HG00735.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2043+190_2043+192d others(5): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAA | 10 | a0001c0001t0001g0157a0001c0001t0001g0196a0001c0001t0001g0206others(7): Show | 10 | HG01071.hp2 HG02293.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2043+189_2043+192d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAAAA | 9 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0128others(6): Show | 10 | HG02922.hp2 HG02965.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.2043+187_2043+192d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAAAAA others(2): Show |
8 | a0001c0001t0001g0026a0001c0001t0001g0084a0001c0001t0001g0085others(5): Show | 8 | HG01952.hp2 HG02135.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.2043+184_2043+192d others(11): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAAAAA others(3): Show |
26 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0031others(23): Show | 26 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.2043+183_2043+192d others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAAAAA others(4): Show |
26 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(23): Show | 27 | HG00558.hp2 HG01928.hp2 HG02004.hp1 others(24): Show |
intron_variant | MODIFIER | c.2043+182_2043+192d others(13): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAAAAA others(5): Show |
15 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0039others(12): Show | 15 | HG00408.hp2 HG01192.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.2043+181_2043+192d others(14): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAAAAA others(6): Show |
7 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0032others(4): Show | 7 | HG00423.hp1 HG02080.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2043+180_2043+192d others(15): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAAAAA others(7): Show |
7 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0079others(4): Show | 7 | HG00673.hp2 NA18954.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2043+179_2043+192d others(16): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2043+178_2043+192d others(17): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0037 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2043+176_2043+192d others(19): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0023 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2043+172_2043+192d others(23): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0038 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2043+171_2043+192d others(24): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0094 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2043+170_2043+192d others(25): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688114
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0001g0210 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2043+181_2043+192d others(14): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 16/19 | chr21 | 31688114 | ||||||
| chr21:31688700
|
C | T | 116 | a0001c0001t0001g0005a0001c0001t0001g0090a0001c0001t0001g0112others(113): Show | 117 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1886-236G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31688700 | ||||||
| chr21:31688714
|
T | A | 1 | a0001c0001t0001g0109 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1886-250A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31688714 | ||||||
| chr21:31688738
|
C | T | 3 | a0001c0003t0002g0001a0001c0003t0002g0016a0001c0011t0001g0325 | 4 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1886-274G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31688738 | ||||||
| chr21:31688966
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1886-502A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31688966 | ||||||
| chr21:31689015
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1886-551C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689015 | ||||||
| chr21:31689417
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1886-953G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689417 | ||||||
| chr21:31689464
|
A | AT | 9 | a0001c0001t0001g0260a0001c0001t0001g0306a0001c0001t0001g0313others(6): Show | 9 | HG01192.hp1 HG01934.hp2 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.1886-1001dupA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689464 | ||||||
| chr21:31689464
|
AT | A | 88 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(85): Show | 90 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.1886-1001delA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689464 | ||||||
| chr21:31689464
|
ATT | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0023others(22): Show | 26 | HG00621.hp1 HG01175.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.1886-1002_1886-100 others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689464 | ||||||
| chr21:31689614
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1886-1150T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689614 | ||||||
| chr21:31689683
|
A | G | 118 | a0001c0001t0001g0005a0001c0001t0001g0090a0001c0001t0001g0112others(115): Show | 119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1885+1114T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689683 | ||||||
| chr21:31689755
|
C | A | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1885+1042G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689755 | ||||||
| chr21:31689787
|
T | C | 10 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(7): Show | 10 | HG01891.hp1 HG01952.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1885+1010A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689787 | ||||||
| chr21:31689792
|
T | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(10): Show | 15 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1885+1005A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31689792 | ||||||
| chr21:31690038
|
T | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(121): Show | 127 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1885+759A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690038 | ||||||
| chr21:31690119
|
C | T | 89 | a0001c0001t0001g0090a0001c0001t0001g0112a0001c0001t0001g0117others(86): Show | 89 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1885+678G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690119 | ||||||
| chr21:31690355
|
C | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(5): Show | 9 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1885+442G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690355 | ||||||
| chr21:31690500
|
A | C | 1 | a0001c0001t0001g0027 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1885+297T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690500 | ||||||
| chr21:31690519
|
C | T | 1 | a0001c0002t0001g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1885+278G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690519 | ||||||
| chr21:31690613
|
G | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1885+184C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690613 | ||||||
| chr21:31690636
|
T | C | 1 | a0001c0004t0001g0010 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1885+161A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690636 | ||||||
| chr21:31690690
|
A | C | 1 | a0001c0002t0001g0203 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1885+107T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 15/19 | chr21 | 31690690 | ||||||
| chr21:31691041
|
C | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(97): Show | 101 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1729-88G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691041 | ||||||
| chr21:31691052
|
C | G | 5 | a0001c0003t0002g0001a0001c0003t0002g0016a0001c0003t0002g0126others(2): Show | 6 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1729-99G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691052 | ||||||
| chr21:31691383
|
A | G | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1729-430T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691383 | ||||||
| chr21:31691394
|
A | G | 2 | a0001c0002t0001g0146a0001c0002t0002g0139 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1728+423T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691394 | ||||||
| chr21:31691672
|
T | TA | 118 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(115): Show | 120 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1728+144dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691672 | ||||||
| chr21:31691672
|
TA | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(18): Show | 22 | HG00738.hp1 HG01070.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1728+144delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691672 | ||||||
| chr21:31691781
|
TA | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(8): Show | 13 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1728+35delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691781 | ||||||
| chr21:31691782
|
A | T | 1 | a0001c0001t0001g0314 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1728+35T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 14/19 | chr21 | 31691782 | ||||||
| chr21:31692138
|
A | T | 1 | a0001c0001t0001g0299 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1615-208T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 13/19 | chr21 | 31692138 | ||||||
| chr21:31692232
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1614+117A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 13/19 | chr21 | 31692232 | ||||||
| chr21:31692705
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1514-256A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 12/19 | chr21 | 31692705 | ||||||
| chr21:31692803
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0225 | 4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1514-354G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 12/19 | chr21 | 31692803 | ||||||
| chr21:31693116
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1513+178C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 12/19 | chr21 | 31693116 | ||||||
| chr21:31693285
|
T | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1513+9A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 12/19 | chr21 | 31693285 | ||||||
| chr21:31693566
|
C | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG02109.hp1 HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1323-82G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 11/19 | chr21 | 31693566 | ||||||
| chr21:31693617
|
A | T | 1 | a0001c0003t0002g0001 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1323-133T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 11/19 | chr21 | 31693617 | ||||||
| chr21:31693821
|
C | A | 88 | a0001c0001t0001g0090a0001c0001t0001g0117a0001c0001t0001g0236others(85): Show | 88 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1323-337G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 11/19 | chr21 | 31693821 | ||||||
| chr21:31694108
|
C | T | 7 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(4): Show | 7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1322+96G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 11/19 | chr21 | 31694108 | ||||||
| chr21:31694110
|
A | G | 4 | a0001c0001t0001g0177a0001c0005t0001g0345a0001c0005t0002g0343others(1): Show | 4 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1322+94T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 11/19 | chr21 | 31694110 | ||||||
| chr21:31694168
|
T | C | 13 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(10): Show | 14 | HG01106.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1322+36A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 11/19 | chr21 | 31694168 | ||||||
| chr21:31694390
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1237-101C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694390 | ||||||
| chr21:31694391
|
C | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0300 | 2 | HG02080.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1237-102G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694391 | ||||||
| chr21:31694441
|
C | G | 2 | a0001c0005t0001g0345a0001c0005t0002g0343 | 2 | HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1237-152G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694441 | ||||||
| chr21:31694463
|
C | T | 1 | a0001c0002t0001g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1237-174G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694463 | ||||||
| chr21:31694483
|
T | A | 1 | a0001c0001t0001g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1237-194A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694483 | ||||||
| chr21:31694607
|
A | G | 1 | a0001c0002t0007g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1236+206T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694607 | ||||||
| chr21:31694620
|
C | T | 1 | a0003c0010t0001g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1236+193G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 10/19 | chr21 | 31694620 | ||||||
| chr21:31695114
|
C | T | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1069-134G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695114 | ||||||
| chr21:31695138
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1069-158G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695138 | ||||||
| chr21:31695398
|
C | T | 111 | a0001c0001t0001g0005a0001c0001t0001g0090a0001c0001t0001g0117others(108): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1069-418G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695398 | ||||||
| chr21:31695455
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1069-475T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695455 | ||||||
| chr21:31695495
|
A | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0045a0001c0001t0001g0096 | 3 | NA18973.hp2 NA18992.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1069-515T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695495 | ||||||
| chr21:31695618
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0077others(2): Show | 5 | HG02257.hp1 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+495G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695618 | ||||||
| chr21:31695999
|
A | G | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1068+114T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31695999 | ||||||
| chr21:31696026
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1068+87G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 9/19 | chr21 | 31696026 | ||||||
| chr21:31696329
|
A | G | 1 | a0001c0003t0002g0001 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.960-108T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/19 | chr21 | 31696329 | ||||||
| chr21:31696338
|
T | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0207 | 2 | NA18974.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.960-117A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/19 | chr21 | 31696338 | ||||||
| chr21:31696393
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.960-172G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/19 | chr21 | 31696393 | ||||||
| chr21:31696508
|
G | C | 2 | a0001c0001t0001g0260a0001c0001t0004g0279 | 2 | NA18967.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.959+61C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 8/19 | chr21 | 31696508 | ||||||
| chr21:31696813
|
T | C | 20 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0151others(17): Show | 20 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.778-63A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31696813 | ||||||
| chr21:31696894
|
C | A | 5 | a0001c0001t0001g0247a0001c0001t0001g0302a0001c0001t0001g0304others(2): Show | 5 | HG00544.hp1 NA18949.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-144G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31696894 | ||||||
| chr21:31697042
|
T | G | 2 | a0001c0002t0001g0014a0001c0002t0001g0227 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.778-292A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697042 | ||||||
| chr21:31697108
|
T | C | 4 | a0001c0001t0001g0104a0001c0001t0002g0103a0001c0001t0006g0017others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-358A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697108 | ||||||
| chr21:31697315
|
C | T | 19 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0151others(16): Show | 19 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.778-565G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697315 | ||||||
| chr21:31697523
|
T | C | 1 | a0001c0003t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.778-773A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697523 | ||||||
| chr21:31697608
|
A | C | 1 | a0001c0002t0001g0214 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.778-858T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697608 | ||||||
| chr21:31697939
|
T | A | 12 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(9): Show | 13 | HG01106.hp1 HG01952.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.778-1189A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697939 | ||||||
| chr21:31697974
|
C | T | 8 | a0001c0002t0001g0179a0001c0002t0001g0180a0001c0002t0001g0181others(5): Show | 8 | NA18942.hp2 NA18945.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.778-1224G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31697974 | ||||||
| chr21:31698024
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.778-1274G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698024 | ||||||
| chr21:31698069
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.778-1319C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698069 | ||||||
| chr21:31698085
|
A | C | 1 | a0001c0001t0006g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.778-1335T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698085 | ||||||
| chr21:31698091
|
G | C | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.778-1341C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698091 | ||||||
| chr21:31698183
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.778-1433C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698183 | ||||||
| chr21:31698205
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.778-1455C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698205 | ||||||
| chr21:31698272
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0092 | 2 | NA18967.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.778-1522A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698272 | ||||||
| chr21:31698346
|
G | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 4 | HG01192.hp2 HG01358.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-1596C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698346 | ||||||
| chr21:31698568
|
T | C | 13 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(10): Show | 14 | HG01106.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-1818A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698568 | ||||||
| chr21:31698703
|
A | G | 13 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(10): Show | 14 | HG01106.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-1953T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698703 | ||||||
| chr21:31698843
|
C | A | 1 | a0001c0001t0001g0024 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.778-2093G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698843 | ||||||
| chr21:31698851
|
A | C | 13 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(10): Show | 14 | HG01106.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-2101T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698851 | ||||||
| chr21:31698983
|
AC | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+2011delG | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31698983 | ||||||
| chr21:31699028
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+1967C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699028 | ||||||
| chr21:31699410
|
A | G | 2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.777+1585T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699410 | ||||||
| chr21:31699501
|
TG | T | 5 | a0001c0004t0001g0186a0001c0004t0001g0187a0001c0004t0001g0188others(2): Show | 5 | HG00639.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+1493delC | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699501 | ||||||
| chr21:31699502
|
G | T | 1 | a0001c0004t0001g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.777+1493C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699502 | ||||||
| chr21:31699502
|
GT | G | 27 | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0001g0240others(24): Show | 27 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.777+1492delA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699502 | ||||||
| chr21:31699502
|
GTT | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(17): Show | 22 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.777+1491_777+1492d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699502 | ||||||
| chr21:31699586
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+1409T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699586 | ||||||
| chr21:31699621
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0330 | 3 | HG01346.hp2 HG01943.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.777+1374C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699621 | ||||||
| chr21:31699717
|
A | T | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.777+1278T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699717 | ||||||
| chr21:31699864
|
T | C | 3 | a0001c0001t0001g0274a0001c0001t0001g0305a0001c0001t0001g0306 | 3 | HG00642.hp2 HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.777+1131A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699864 | ||||||
| chr21:31699887
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.777+1108C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699887 | ||||||
| chr21:31699975
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0002g0103a0001c0001t0006g0017 | 3 | HG03098.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.777+1020G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699975 | ||||||
| chr21:31699988
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+1007C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31699988 | ||||||
| chr21:31700050
|
T | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(96): Show | 100 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.777+945A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700050 | ||||||
| chr21:31700123
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.777+872C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700123 | ||||||
| chr21:31700158
|
AC | A | 9 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0191others(6): Show | 9 | HG01071.hp2 HG01928.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.777+836delG | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700158 | ||||||
| chr21:31700182
|
T | TCA | 130 | a0001c0001t0001g0005a0001c0001t0001g0090a0001c0001t0001g0112others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.777+811_777+812dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700182 | ||||||
| chr21:31700234
|
AAAT | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+758_777+760del others(3): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700234 | ||||||
| chr21:31700290
|
C | G | 2 | a0001c0003t0001g0118a0001c0003t0001g0119 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.777+705G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700290 | ||||||
| chr21:31700351
|
C | T | 1 | a0001c0004t0001g0011 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.777+644G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700351 | ||||||
| chr21:31700352
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.777+643C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700352 | ||||||
| chr21:31700410
|
G | C | 2 | a0001c0003t0001g0125a0001c0003t0002g0126 | 2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.777+585C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700410 | ||||||
| chr21:31700544
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.777+451T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700544 | ||||||
| chr21:31700570
|
T | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+425A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700570 | ||||||
| chr21:31700574
|
A | G | 1 | a0001c0003t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.777+421T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700574 | ||||||
| chr21:31700741
|
C | CT | 19 | a0001c0001t0001g0003a0001c0001t0001g0091a0001c0001t0001g0127others(16): Show | 21 | HG01106.hp1 HG01109.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.777+253dupA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700741 | ||||||
| chr21:31700741
|
C | CTT | 8 | a0001c0002t0001g0181a0001c0003t0001g0118a0001c0003t0001g0119others(5): Show | 8 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.777+252_777+253dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700741 | ||||||
| chr21:31700812
|
A | T | 3 | a0002c0006t0001g0277a0002c0006t0001g0308a0002c0006t0001g0326 | 3 | HG01074.hp2 HG01243.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.777+183T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 7/19 | chr21 | 31700812 | ||||||
| chr21:31701350
|
T | C | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.601-179A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 6/19 | chr21 | 31701350 | ||||||
| chr21:31701479
|
G | A | 1 | a0002c0006t0001g0326 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.600+297C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 6/19 | chr21 | 31701479 | ||||||
| chr21:31701608
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.600+168G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 6/19 | chr21 | 31701608 | ||||||
| chr21:31701630
|
A | C | 10 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(7): Show | 10 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.600+146T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 6/19 | chr21 | 31701630 | ||||||
| chr21:31701698
|
T | C | 5 | a0001c0004t0001g0186a0001c0004t0001g0187a0001c0004t0001g0188others(2): Show | 5 | HG02723.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+78A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 6/19 | chr21 | 31701698 | ||||||
| chr21:31701737
|
A | C | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.600+39T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 6/19 | chr21 | 31701737 | ||||||
| chr21:31702034
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.458-116C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 5/19 | chr21 | 31702034 | ||||||
| chr21:31702382
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG02647.hp2 | splice_region_variant&intron_variant | LOW | c.322-3C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31702382 | ||||||
| chr21:31702528
|
A | G | 3 | a0001c0001t0001g0151a0001c0001t0001g0195a0001c0001t0001g0199 | 3 | HG00099.hp1 HG01978.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.322-149T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31702528 | ||||||
| chr21:31702611
|
A | G | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.322-232T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31702611 | ||||||
| chr21:31702733
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322-354T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31702733 | ||||||
| chr21:31702904
|
A | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(5): Show | 9 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.322-525T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31702904 | ||||||
| chr21:31702968
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.322-589A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31702968 | ||||||
| chr21:31703091
|
T | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(115): Show | 120 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.321+674A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703091 | ||||||
| chr21:31703114
|
A | C | 9 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(6): Show | 9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.321+651T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703114 | ||||||
| chr21:31703192
|
C | CA | 118 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(115): Show | 120 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.321+572dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703192 | ||||||
| chr21:31703239
|
A | C | 2 | a0001c0003t0001g0125a0001c0003t0002g0126 | 2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.321+526T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703239 | ||||||
| chr21:31703290
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.321+475G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703290 | ||||||
| chr21:31703330
|
A | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(237): Show | 244 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.321+435T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703330 | ||||||
| chr21:31703356
|
T | C | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.321+409A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703356 | ||||||
| chr21:31703629
|
A | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(9): Show | 13 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.321+136T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 4/19 | chr21 | 31703629 | ||||||
| chr21:31704261
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0330 | 3 | HG01346.hp2 HG01943.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.160-335G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704261 | ||||||
| chr21:31704336
|
C | G | 1 | a0001c0002t0001g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.160-410G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704336 | ||||||
| chr21:31704532
|
C | CA | 13 | a0001c0001t0001g0023a0001c0001t0001g0195a0001c0001t0001g0275others(10): Show | 13 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.160-607dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704532 | ||||||
| chr21:31704532
|
C | CAA | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-608_160-607dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704532 | ||||||
| chr21:31704558
|
A | C | 1 | a0001c0013t0001g0281 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.160-632T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704558 | ||||||
| chr21:31704594
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.160-668G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704594 | ||||||
| chr21:31704620
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.160-694T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704620 | ||||||
| chr21:31704621
|
C | T | 329 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(326): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.160-695G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704621 | ||||||
| chr21:31704636
|
G | A | 1 | a0001c0002t0001g0142 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.160-710C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704636 | ||||||
| chr21:31704651
|
A | T | 1 | a0001c0002t0001g0180 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.160-725T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704651 | ||||||
| chr21:31704710
|
A | G | 12 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(9): Show | 13 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+713T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 3/19 | chr21 | 31704710 | ||||||
| chr21:31705500
|
TTTAC | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0225 | 4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-37_115-34delGT others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31705500 | ||||||
| chr21:31705526
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.115-59A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31705526 | ||||||
| chr21:31705551
|
T | C | 1 | a0001c0002t0001g0168 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.115-84A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31705551 | ||||||
| chr21:31705957
|
C | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(203): Show | 208 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.114+317G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31705957 | ||||||
| chr21:31706037
|
T | C | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.114+237A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31706037 | ||||||
| chr21:31706052
|
G | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0038others(19): Show | 23 | HG00738.hp1 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.114+222C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31706052 | ||||||
| chr21:31706168
|
T | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA19057.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.114+106A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31706168 | ||||||
| chr21:31706175
|
G | A | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.114+99C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 2/19 | chr21 | 31706175 | ||||||
| chr21:31706414
|
G | C | 7 | a0001c0001t0001g0074a0001c0001t0001g0105a0001c0001t0001g0318others(4): Show | 8 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-57C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706414 | ||||||
| chr21:31706424
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.31-67A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706424 | ||||||
| chr21:31706473
|
AG | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 10 | HG02109.hp1 HG02615.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-117delC | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706473 | ||||||
| chr21:31706513
|
T | C | 23 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0104others(20): Show | 23 | HG00639.hp2 HG01109.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.31-156A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706513 | ||||||
| chr21:31706600
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.31-243C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706600 | ||||||
| chr21:31706612
|
G | A | 107 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0032others(104): Show | 109 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.31-255C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706612 | ||||||
| chr21:31706629
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.31-272C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706629 | ||||||
| chr21:31706660
|
A | G | 4 | a0001c0001t0001g0223a0001c0003t0002g0001a0001c0003t0002g0016others(1): Show | 5 | HG01106.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-303T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706660 | ||||||
| chr21:31706803
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.31-446G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706803 | ||||||
| chr21:31706816
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0002g0103a0001c0001t0006g0017 | 3 | HG03098.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.31-459T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706816 | ||||||
| chr21:31706827
|
T | TC | 6 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(3): Show | 6 | HG02622.hp1 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-471dupG | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706827 | ||||||
| chr21:31706842
|
A | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG02486.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.31-485T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706842 | ||||||
| chr21:31706893
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-536C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31706893 | ||||||
| chr21:31707001
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.31-644T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707001 | ||||||
| chr21:31707153
|
T | C | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-796A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707153 | ||||||
| chr21:31707312
|
C | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(5): Show | 9 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-955G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707312 | ||||||
| chr21:31707445
|
A | G | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-1088T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707445 | ||||||
| chr21:31707480
|
T | TAAGG | 9 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 10 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-1124_31-1123ins others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707480 | ||||||
| chr21:31707488
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31-1131T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707488 | ||||||
| chr21:31707526
|
C | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-1169G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707526 | ||||||
| chr21:31707717
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.31-1360A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707717 | ||||||
| chr21:31707770
|
C | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-1413G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31707770 | ||||||
| chr21:31708000
|
G | A | 65 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(62): Show | 65 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.31-1643C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708000 | ||||||
| chr21:31708125
|
T | C | 7 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(4): Show | 7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-1768A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708125 | ||||||
| chr21:31708196
|
T | C | 2 | a0001c0001t0003g0169a0001c0001t0003g0215 | 2 | HG00642.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.31-1839A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708196 | ||||||
| chr21:31708277
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.31-1920C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708277 | ||||||
| chr21:31708290
|
C | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-1933G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708290 | ||||||
| chr21:31708290
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.31-1933G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708290 | ||||||
| chr21:31708308
|
G | A | 1 | a0001c0003t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.31-1951C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708308 | ||||||
| chr21:31708437
|
T | C | 6 | a0001c0001t0001g0104a0001c0001t0002g0103a0001c0001t0006g0017others(3): Show | 7 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-2080A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708437 | ||||||
| chr21:31708526
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-2169A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708526 | ||||||
| chr21:31708665
|
C | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-2308G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708665 | ||||||
| chr21:31708678
|
C | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-2321G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708678 | ||||||
| chr21:31708860
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.31-2503T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708860 | ||||||
| chr21:31708891
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.31-2534C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31708891 | ||||||
| chr21:31709144
|
T | C | 2 | a0001c0001t0001g0260a0001c0001t0004g0279 | 2 | NA18967.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.31-2787A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709144 | ||||||
| chr21:31709202
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-2845C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709202 | ||||||
| chr21:31709268
|
C | T | 1 | a0001c0002t0001g0012 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.31-2911G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709268 | ||||||
| chr21:31709350
|
C | CA | 18 | a0001c0001t0001g0004a0001c0001t0001g0105a0001c0001t0001g0171others(15): Show | 19 | HG01074.hp1 HG01167.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.31-2994dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709350 | ||||||
| chr21:31709350
|
C | CAA | 12 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0038others(9): Show | 13 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-2995_31-2994dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709350 | ||||||
| chr21:31709350
|
C | CAAA | 86 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(83): Show | 87 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.31-2996_31-2994dup others(3): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709350 | ||||||
| chr21:31709361
|
A | G | 7 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(4): Show | 7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-3004T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709361 | ||||||
| chr21:31709692
|
C | A | 1 | a0001c0001t0001g0046 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.31-3335G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709692 | ||||||
| chr21:31709774
|
G | C | 2 | a0001c0001t0001g0245a0001c0001t0001g0292 | 2 | NA18998.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.31-3417C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709774 | ||||||
| chr21:31709844
|
AGAT | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(104): Show | 109 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.31-3490_31-3488del others(3): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709844 | ||||||
| chr21:31709854
|
TA | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(31): Show | 36 | HG00738.hp1 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.31-3498delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709854 | ||||||
| chr21:31709874
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.31-3517G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31709874 | ||||||
| chr21:31710029
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(95): Show | 99 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.31-3672A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710029 | ||||||
| chr21:31710069
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.31-3712G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710069 | ||||||
| chr21:31710156
|
T | C | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3799A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710156 | ||||||
| chr21:31710181
|
C | G | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-3824G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710181 | ||||||
| chr21:31710219
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-3862C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710219 | ||||||
| chr21:31710319
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.31-3962G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710319 | ||||||
| chr21:31710481
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.31-4124C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710481 | ||||||
| chr21:31710749
|
G | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.31-4392C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31710749 | ||||||
| chr21:31711205
|
C | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0300 | 2 | HG02080.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.31-4848G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31711205 | ||||||
| chr21:31711461
|
T | C | 1 | a0001c0002t0001g0170 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.31-5104A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31711461 | ||||||
| chr21:31711515
|
T | C | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-5158A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31711515 | ||||||
| chr21:31711729
|
A | C | 2 | a0001c0001t0001g0216a0001c0001t0004g0217 | 2 | HG01496.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.31-5372T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31711729 | ||||||
| chr21:31711944
|
A | G | 87 | a0001c0001t0001g0117a0001c0001t0001g0236a0001c0001t0001g0237others(84): Show | 87 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.31-5587T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31711944 | ||||||
| chr21:31711987
|
T | C | 1 | a0001c0002t0001g0161 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.31-5630A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31711987 | ||||||
| chr21:31712039
|
T | G | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-5682A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712039 | ||||||
| chr21:31712047
|
T | G | 2 | a0001c0002t0001g0013a0001c0002t0001g0014 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.31-5690A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712047 | ||||||
| chr21:31712222
|
C | CT | 310 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(307): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.31-5866dupA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712222 | ||||||
| chr21:31712222
|
C | CTT | 6 | a0001c0001t0001g0174a0001c0001t0001g0284a0001c0001t0001g0302others(3): Show | 6 | HG03239.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-5867_31-5866dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712222 | ||||||
| chr21:31712222
|
C | CTTTTTTT others(5): Show |
1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-5877_31-5866dup others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712222 | ||||||
| chr21:31712308
|
C | A | 110 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0236others(107): Show | 111 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.31-5951G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712308 | ||||||
| chr21:31712362
|
C | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-6005G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712362 | ||||||
| chr21:31712373
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-6016T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712373 | ||||||
| chr21:31712410
|
G | T | 1 | a0007c0016t0001g0282 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.31-6053C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712410 | ||||||
| chr21:31712527
|
C | CT | 23 | a0001c0001t0001g0091a0001c0001t0001g0131a0001c0001t0001g0136others(20): Show | 23 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.31-6171dupA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712527 | ||||||
| chr21:31712527
|
C | CTT | 7 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(4): Show | 7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-6172_31-6171dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712527 | ||||||
| chr21:31712527
|
CT | C | 6 | a0001c0001t0001g0084a0001c0001t0002g0068a0001c0003t0001g0125others(3): Show | 7 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-6171delA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712527 | ||||||
| chr21:31712527
|
CTT | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-6172_31-6171del others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712527 | ||||||
| chr21:31712789
|
C | CAA | 3 | a0001c0001t0002g0261a0001c0007t0001g0293a0001c0007t0001g0323 | 3 | NA18954.hp1 NA18974.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.31-6434_31-6433dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712789 | ||||||
| chr21:31712809
|
C | T | 1 | a0001c0003t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.31-6452G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712809 | ||||||
| chr21:31712898
|
A | T | 1 | a0001c0001t0001g0050 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.31-6541T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712898 | ||||||
| chr21:31712904
|
T | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-6547A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31712904 | ||||||
| chr21:31713019
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.31-6662T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713019 | ||||||
| chr21:31713112
|
TTACTTGT others(10): Show |
T | 1 | a0001c0002t0002g0139 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.31-6772_31-6756del others(17): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713112 | ||||||
| chr21:31713272
|
G | A | 110 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0236others(107): Show | 111 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.31-6915C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713272 | ||||||
| chr21:31713380
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0001g0252a0001c0001t0001g0283others(1): Show | 4 | HG02135.hp2 NA19000.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-7023A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713380 | ||||||
| chr21:31713484
|
C | T | 19 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0151others(16): Show | 19 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.31-7127G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713484 | ||||||
| chr21:31713505
|
A | G | 2 | a0001c0001t0001g0106a0001c0011t0001g0325 | 2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-7148T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713505 | ||||||
| chr21:31713541
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.31-7184T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713541 | ||||||
| chr21:31713741
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0292 | 2 | NA18998.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.31-7384C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713741 | ||||||
| chr21:31713745
|
C | T | 5 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0005t0001g0345others(2): Show | 5 | HG00738.hp1 HG01099.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-7388G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713745 | ||||||
| chr21:31713746
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-7389C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713746 | ||||||
| chr21:31713756
|
T | TG | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(140): Show | 145 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.31-7400dupC | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713756 | ||||||
| chr21:31713763
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-7406C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713763 | ||||||
| chr21:31713815
|
A | G | 3 | a0001c0001t0001g0171a0001c0004t0001g0009a0001c0004t0001g0010 | 3 | HG01891.hp2 HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.31-7458T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713815 | ||||||
| chr21:31713819
|
T | G | 1 | a0001c0003t0001g0122 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.31-7462A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713819 | ||||||
| chr21:31713864
|
G | C | 7 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(4): Show | 7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-7507C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713864 | ||||||
| chr21:31713960
|
T | C | 1 | a0001c0002t0001g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.31-7603A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31713960 | ||||||
| chr21:31714026
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.31-7669C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714026 | ||||||
| chr21:31714078
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.31-7721T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714078 | ||||||
| chr21:31714126
|
T | C | 346 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(343): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.31-7769A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714126 | ||||||
| chr21:31714184
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-7827T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714184 | ||||||
| chr21:31714344
|
T | C | 25 | a0001c0001t0001g0117a0001c0001t0001g0248a0001c0001t0001g0249others(22): Show | 25 | HG00642.hp2 HG01081.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.31-7987A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714344 | ||||||
| chr21:31714478
|
G | A | 1 | a0001c0003t0005g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.31-8121C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714478 | ||||||
| chr21:31714493
|
C | T | 1 | a0001c0002t0001g0161 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.31-8136G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714493 | ||||||
| chr21:31714526
|
C | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-8169G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714526 | ||||||
| chr21:31714554
|
T | C | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-8197A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714554 | ||||||
| chr21:31714995
|
T | C | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.31-8638A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31714995 | ||||||
| chr21:31715044
|
G | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0023others(23): Show | 27 | HG00621.hp1 HG01175.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.31-8687C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715044 | ||||||
| chr21:31715108
|
T | C | 110 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0236others(107): Show | 111 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.31-8751A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715108 | ||||||
| chr21:31715250
|
C | A | 9 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(6): Show | 9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-8893G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715250 | ||||||
| chr21:31715550
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 10 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-9193T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715550 | ||||||
| chr21:31715642
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-9285G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715642 | ||||||
| chr21:31715703
|
G | A | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-9346C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715703 | ||||||
| chr21:31715928
|
G | A | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(120): Show | 126 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.31-9571C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31715928 | ||||||
| chr21:31716048
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.31-9691C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716048 | ||||||
| chr21:31716164
|
CT | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-9808delA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716164 | ||||||
| chr21:31716280
|
G | C | 1 | a0001c0001t0002g0324 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.31-9923C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716280 | ||||||
| chr21:31716580
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.31-10223G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716580 | ||||||
| chr21:31716582
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.31-10225G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716582 | ||||||
| chr21:31716697
|
AG | A | 3 | a0001c0001t0002g0261a0001c0007t0001g0293a0001c0007t0001g0323 | 3 | NA18954.hp1 NA18974.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.31-10341delC | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716697 | ||||||
| chr21:31716808
|
A | G | 2 | a0001c0003t0001g0118a0001c0003t0001g0119 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.31-10451T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31716808 | ||||||
| chr21:31717033
|
T | C | 9 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(6): Show | 9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-10676A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717033 | ||||||
| chr21:31717095
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.31-10738G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717095 | ||||||
| chr21:31717149
|
G | A | 2 | a0001c0003t0001g0118a0001c0003t0001g0119 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.31-10792C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717149 | ||||||
| chr21:31717390
|
A | C | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-11033T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717390 | ||||||
| chr21:31717795
|
A | C | 1 | a0001c0001t0001g0280 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.31-11438T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717795 | ||||||
| chr21:31717806
|
A | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-11449T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717806 | ||||||
| chr21:31717807
|
A | T | 3 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0011t0001g0325 | 3 | HG00639.hp1 HG02970.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.31-11450T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717807 | ||||||
| chr21:31717826
|
C | CAT | 20 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0045others(17): Show | 20 | HG00140.hp2 HG00639.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-11471_31-11470d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717826 | ||||||
| chr21:31717826
|
C | CATATAT | 40 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(37): Show | 40 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.31-11475_31-11470d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717826 | ||||||
| chr21:31717826
|
C | CATATATA others(1): Show |
6 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0108others(3): Show | 6 | HG00544.hp2 HG02074.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-11477_31-11470d others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717826 | ||||||
| chr21:31717826
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.31-11481_31-11470d others(14): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717826 | ||||||
| chr21:31717826
|
CATAT | C | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-11473_31-11470d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717826 | ||||||
| chr21:31717840
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-11483A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717840 | ||||||
| chr21:31717840
|
T | TAC | 7 | a0001c0001t0001g0172a0001c0001t0001g0246a0001c0001t0001g0257others(4): Show | 7 | HG02040.hp2 HG02602.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-11484_31-11483i others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717840 | ||||||
| chr21:31717842
|
T | C | 14 | a0001c0001t0001g0117a0001c0001t0001g0135a0001c0001t0001g0172others(11): Show | 14 | HG00544.hp1 HG01496.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.31-11485A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | ||||||
| chr21:31717842
|
T | TAC | 108 | a0001c0001t0001g0004a0001c0001t0001g0132a0001c0001t0001g0156others(105): Show | 109 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.31-11487_31-11486d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | ||||||
| chr21:31717842
|
T | TACAC | 24 | a0001c0001t0001g0131a0001c0001t0001g0133a0001c0001t0001g0134others(21): Show | 24 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.31-11489_31-11486d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | ||||||
| chr21:31717842
|
T | TACACAC | 6 | a0001c0001t0001g0136a0001c0001t0001g0191a0001c0001t0001g0196others(3): Show | 6 | HG01071.hp2 HG01928.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-11491_31-11486d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | ||||||
| chr21:31717842
|
T | TATAC | 22 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0193others(19): Show | 22 | HG00642.hp2 HG01081.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.31-11486_31-11485i others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | ||||||
| chr21:31717842
|
T | TATATAC | 4 | a0001c0001t0001g0059a0001c0001t0001g0080a0001c0001t0001g0085others(1): Show | 4 | HG02273.hp2 NA18963.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-11486_31-11485i others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | ||||||
| chr21:31717842
|
T | TATATATA others(1): Show |
3 | a0001c0001t0001g0058a0001c0001t0001g0079a0001c0001t0001g0081 | 3 | HG01167.hp2 HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.31-11486_31-11485i others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | ||||||
| chr21:31717842
|
T | TATATATA others(3): Show |
1 | a0001c0001t0001g0097 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.31-11486_31-11485i others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | ||||||
| chr21:31717842
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0057 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.31-11486_31-11485i others(14): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717842 | ||||||
| chr21:31717844
|
C | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(80): Show | 87 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.31-11487G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717844 | ||||||
| chr21:31717846
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0020others(62): Show | 67 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.31-11489G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717846 | ||||||
| chr21:31717848
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0020others(54): Show | 59 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.31-11491G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717848 | ||||||
| chr21:31717850
|
C | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0023others(32): Show | 36 | HG00621.hp1 HG00639.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.31-11493G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717850 | ||||||
| chr21:31717852
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 27 | HG00621.hp1 HG01175.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.31-11495G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717852 | ||||||
| chr21:31717854
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0084a0001c0001t0001g0087 | 3 | HG03834.hp2 HG04115.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.31-11497G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717854 | ||||||
| chr21:31717856
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.31-11499G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717856 | ||||||
| chr21:31717860
|
C | T | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-11503G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717860 | ||||||
| chr21:31717862
|
C | T | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-11505G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717862 | ||||||
| chr21:31717864
|
C | T | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-11507G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717864 | ||||||
| chr21:31717864
|
CACACACA others(3): Show |
C | 2 | a0001c0003t0001g0118a0001c0003t0001g0119 | 2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.31-11517_31-11508d others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717864 | ||||||
| chr21:31717866
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 8 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-11509G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717866 | ||||||
| chr21:31717866
|
CACACATA others(1): Show |
C | 9 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0106others(6): Show | 9 | HG01243.hp1 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-11517_31-11510d others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717866 | ||||||
| chr21:31717868
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(64): Show | 68 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.31-11511G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717868 | ||||||
| chr21:31717870
|
C | T | 71 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(68): Show | 72 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.31-11513G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717870 | ||||||
| chr21:31717870
|
CAT | C | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0105others(2): Show | 6 | HG01106.hp1 HG02451.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-11515_31-11514d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717870 | ||||||
| chr21:31717870
|
CATAT | C | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG00423.hp1 HG00738.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.31-11517_31-11514d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717870 | ||||||
| chr21:31717872
|
T | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0020others(50): Show | 55 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.31-11515A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717872 | ||||||
| chr21:31717874
|
T | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(56): Show | 63 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.31-11517A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717874 | ||||||
| chr21:31717876
|
C | T | 2 | a0001c0003t0001g0120a0001c0003t0001g0122 | 2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.31-11519G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717876 | ||||||
| chr21:31717878
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0023others(48): Show | 53 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.31-11521G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717878 | ||||||
| chr21:31717880
|
T | C | 10 | a0001c0001t0001g0154a0001c0001t0001g0198a0001c0002t0001g0146others(7): Show | 10 | HG02015.hp2 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-11523A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717880 | ||||||
| chr21:31717880
|
TATATACA others(1): Show |
T | 4 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 5 | HG02615.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-11531_31-11524d others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717880 | ||||||
| chr21:31717886
|
C | T | 2 | a0001c0003t0001g0120a0001c0003t0001g0122 | 2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.31-11529G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717886 | ||||||
| chr21:31717888
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31-11531G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717888 | ||||||
| chr21:31717890
|
T | C | 2 | a0001c0003t0001g0120a0001c0003t0001g0122 | 2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.31-11533A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717890 | ||||||
| chr21:31717890
|
TATATACA others(19): Show |
T | 1 | a0001c0003t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.31-11559_31-11534d others(28): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717890 | ||||||
| chr21:31717892
|
T | C | 1 | a0001c0003t0001g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.31-11535A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717892 | ||||||
| chr21:31717892
|
TATACACA others(15): Show |
T | 1 | a0001c0001t0006g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-11557_31-11536d others(24): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717892 | ||||||
| chr21:31717894
|
T | C | 4 | a0001c0003t0001g0120a0001c0003t0001g0122a0001c0003t0001g0123others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-11537A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717894 | ||||||
| chr21:31717896
|
CACATATA others(1): Show |
C | 4 | a0001c0002t0001g0146a0001c0002t0001g0202a0001c0002t0002g0139others(1): Show | 4 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-11547_31-11540d others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717896 | ||||||
| chr21:31717898
|
C | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-11541G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717898 | ||||||
| chr21:31717898
|
CAT | C | 15 | a0001c0001t0001g0033a0001c0001t0001g0065a0001c0001t0001g0066others(12): Show | 15 | HG00621.hp2 HG01081.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-11543_31-11542d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717898 | ||||||
| chr21:31717898
|
CATATAT | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0002t0001g0150others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-11547_31-11542d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717898 | ||||||
| chr21:31717900
|
T | C | 4 | a0001c0002t0001g0148a0001c0003t0001g0121a0001c0003t0001g0123others(1): Show | 4 | HG00741.hp2 HG01952.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-11543A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717900 | ||||||
| chr21:31717900
|
TATATACA others(5): Show |
T | 1 | a0001c0003t0002g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.31-11555_31-11544d others(14): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717900 | ||||||
| chr21:31717902
|
T | C | 6 | a0001c0002t0001g0148a0001c0003t0001g0118a0001c0003t0001g0119others(3): Show | 6 | HG00741.hp2 HG01952.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-11545A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717902 | ||||||
| chr21:31717902
|
T | TAC | 4 | a0001c0001t0002g0103a0001c0002t0007g0346a0001c0003t0005g0021others(1): Show | 4 | HG01891.hp1 HG01934.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-11546_31-11545i others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717902 | ||||||
| chr21:31717902
|
T | TACAC | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0104others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-11546_31-11545i others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717902 | ||||||
| chr21:31717902
|
TATAC | T | 24 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0047others(21): Show | 24 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-11549_31-11546d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717902 | ||||||
| chr21:31717902
|
TATACAC | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0091others(8): Show | 11 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-11551_31-11546d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717902 | ||||||
| chr21:31717904
|
T | C | 26 | a0001c0001t0001g0018a0001c0001t0001g0071a0001c0001t0001g0075others(23): Show | 26 | HG00741.hp2 HG01891.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.31-11547A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | ||||||
| chr21:31717904
|
T | TAC | 18 | a0001c0001t0001g0172a0001c0001t0001g0175a0001c0001t0001g0176others(15): Show | 18 | HG00735.hp2 HG00738.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.31-11549_31-11548d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | ||||||
| chr21:31717904
|
T | TACAC | 9 | a0001c0001t0001g0223a0001c0001t0001g0248a0001c0001t0001g0278others(6): Show | 9 | HG00741.hp1 HG01074.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-11551_31-11548d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | ||||||
| chr21:31717904
|
T | TACACAC | 11 | a0001c0001t0001g0268a0001c0001t0001g0274a0001c0001t0001g0300others(8): Show | 11 | HG00642.hp2 HG01081.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-11553_31-11548d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | ||||||
| chr21:31717904
|
T | TACACACA others(3): Show |
4 | a0001c0001t0001g0225a0001c0001t0001g0249a0001c0002t0001g0214others(1): Show | 4 | HG00639.hp2 HG01168.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-11557_31-11548d others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | ||||||
| chr21:31717904
|
TAC | T | 68 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0040others(65): Show | 69 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.31-11549_31-11548d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | ||||||
| chr21:31717904
|
TACAC | T | 42 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0131others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.31-11551_31-11548d others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | ||||||
| chr21:31717904
|
TACACAC | T | 13 | a0001c0001t0001g0134a0001c0001t0001g0156a0001c0001t0001g0157others(10): Show | 13 | HG01358.hp2 HG01934.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.31-11553_31-11548d others(8): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | ||||||
| chr21:31717904
|
TACACACA others(1): Show |
T | 4 | a0001c0001t0001g0117a0001c0001t0001g0137a0001c0001t0001g0238others(1): Show | 4 | HG00140.hp1 HG03831.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-11555_31-11548d others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | ||||||
| chr21:31717904
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0039 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.31-11557_31-11548d others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | ||||||
| chr21:31717904
|
TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0319a0001c0001t0003g0007a0001c0001t0003g0333 | 3 | HG02818.hp1 HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.31-11559_31-11548d others(14): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | ||||||
| chr21:31717904
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0154 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.31-11561_31-11548d others(16): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717904 | ||||||
| chr21:31717906
|
C | T | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-11549G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717906 | ||||||
| chr21:31717908
|
C | CAT | 28 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0023others(25): Show | 29 | HG00423.hp1 HG00621.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.31-11552_31-11551i others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717908 | ||||||
| chr21:31717910
|
C | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0020others(35): Show | 41 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.31-11553G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717910 | ||||||
| chr21:31717912
|
C | T | 33 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0025others(30): Show | 36 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.31-11555G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717912 | ||||||
| chr21:31717914
|
C | T | 28 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0037others(25): Show | 29 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.31-11557G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717914 | ||||||
| chr21:31717916
|
C | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0038others(18): Show | 22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.31-11559G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717916 | ||||||
| chr21:31717918
|
C | T | 1 | a0001c0001t0001g0338 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.31-11561G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717918 | ||||||
| chr21:31717920
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.31-11563G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717920 | ||||||
| chr21:31717922
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.31-11565G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717922 | ||||||
| chr21:31717938
|
CACACACA others(3): Show |
C | 4 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 5 | HG02615.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-11591_31-11582d others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717938 | ||||||
| chr21:31717940
|
CACACACA others(1): Show |
C | 4 | a0001c0001t0001g0129a0001c0001t0001g0178a0001c0002t0001g0149others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-11591_31-11584d others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717940 | ||||||
| chr21:31717946
|
CAT | C | 7 | a0001c0001t0001g0174a0001c0001t0001g0218a0001c0001t0001g0224others(4): Show | 7 | HG01074.hp1 HG01099.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-11591_31-11590d others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717946 | ||||||
| chr21:31717948
|
T | C | 7 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0093others(4): Show | 7 | HG02486.hp1 HG02818.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-11591A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31717948 | ||||||
| chr21:31718069
|
A | G | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-11712T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718069 | ||||||
| chr21:31718108
|
T | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-11751A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718108 | ||||||
| chr21:31718366
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.31-12009A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718366 | ||||||
| chr21:31718445
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(95): Show | 99 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.31-12088C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718445 | ||||||
| chr21:31718472
|
T | C | 7 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(4): Show | 7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-12115A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718472 | ||||||
| chr21:31718505
|
A | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(92): Show | 96 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.31-12148T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718505 | ||||||
| chr21:31718575
|
C | T | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.31-12218G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718575 | ||||||
| chr21:31718651
|
G | A | 2 | a0001c0001t0001g0099a0001c0003t0002g0126 | 2 | HG03225.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.31-12294C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718651 | ||||||
| chr21:31718771
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-12414G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718771 | ||||||
| chr21:31718780
|
T | C | 1 | a0001c0004t0001g0011 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.31-12423A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718780 | ||||||
| chr21:31718976
|
T | C | 1 | a0001c0001t0004g0192 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.31-12619A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31718976 | ||||||
| chr21:31719120
|
A | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(120): Show | 126 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.30+12543T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719120 | ||||||
| chr21:31719161
|
A | G | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+12502T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719161 | ||||||
| chr21:31719289
|
C | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+12374G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719289 | ||||||
| chr21:31719322
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+12341T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719322 | ||||||
| chr21:31719459
|
T | G | 1 | a0001c0001t0001g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.30+12204A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719459 | ||||||
| chr21:31719498
|
A | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0104a0001c0001t0001g0127others(7): Show | 11 | HG02615.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+12165T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719498 | ||||||
| chr21:31719501
|
C | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0092 | 3 | HG02155.hp1 NA18967.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.30+12162G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719501 | ||||||
| chr21:31719608
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0003g0169a0001c0001t0003g0215 | 3 | HG00642.hp1 HG00735.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.30+12055C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719608 | ||||||
| chr21:31719710
|
G | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+11953C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719710 | ||||||
| chr21:31719774
|
G | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+11889C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719774 | ||||||
| chr21:31719953
|
T | G | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+11710A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31719953 | ||||||
| chr21:31720200
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.30+11463A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720200 | ||||||
| chr21:31720455
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.30+11208G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720455 | ||||||
| chr21:31720468
|
G | A | 4 | a0001c0001t0001g0104a0001c0001t0002g0103a0001c0001t0006g0017others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+11195C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720468 | ||||||
| chr21:31720468
|
G | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0116 | 2 | NA18977.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.30+11195C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720468 | ||||||
| chr21:31720530
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0171a0001c0001t0001g0172others(12): Show | 16 | HG01074.hp1 HG01167.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.30+11133C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720530 | ||||||
| chr21:31720737
|
T | C | 8 | a0001c0002t0001g0179a0001c0002t0001g0180a0001c0002t0001g0181others(5): Show | 8 | NA18942.hp2 NA18945.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+10926A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720737 | ||||||
| chr21:31720893
|
A | G | 1 | a0001c0001t0004g0192 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.30+10770T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31720893 | ||||||
| chr21:31721219
|
T | C | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+10444A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721219 | ||||||
| chr21:31721303
|
T | C | 12 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(9): Show | 12 | HG02257.hp1 HG02622.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+10360A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721303 | ||||||
| chr21:31721307
|
GTGATTTA others(15): Show |
G | 1 | a0001c0001t0004g0036 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.30+10334_30+10355d others(24): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721307 | ||||||
| chr21:31721725
|
C | CT | 97 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0093others(94): Show | 97 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.30+9937dupA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721725 | ||||||
| chr21:31721726
|
T | C | 1 | a0001c0003t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.30+9937A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721726 | ||||||
| chr21:31721758
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+9905C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721758 | ||||||
| chr21:31721767
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.30+9896G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721767 | ||||||
| chr21:31721783
|
C | A | 346 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(343): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.30+9880G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721783 | ||||||
| chr21:31721784
|
A | C | 346 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(343): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.30+9879T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31721784 | ||||||
| chr21:31722000
|
G | T | 1 | a0001c0003t0002g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.30+9663C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722000 | ||||||
| chr21:31722417
|
T | C | 6 | a0001c0004t0001g0186a0001c0004t0001g0187a0001c0004t0001g0188others(3): Show | 6 | HG00639.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+9246A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722417 | ||||||
| chr21:31722519
|
C | T | 1 | a0001c0002t0004g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.30+9144G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722519 | ||||||
| chr21:31722745
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 10 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+8918T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722745 | ||||||
| chr21:31722774
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+8889C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722774 | ||||||
| chr21:31722810
|
G | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0106 | 3 | HG01243.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.30+8853C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722810 | ||||||
| chr21:31722884
|
C | T | 1 | a0001c0003t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.30+8779G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31722884 | ||||||
| chr21:31723051
|
A | G | 1 | a0001c0002t0001g0153 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.30+8612T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723051 | ||||||
| chr21:31723106
|
T | A | 7 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(4): Show | 7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+8557A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723106 | ||||||
| chr21:31723172
|
T | C | 2 | a0001c0003t0002g0001a0001c0003t0002g0016 | 3 | HG01106.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.30+8491A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723172 | ||||||
| chr21:31723298
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.30+8365T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723298 | ||||||
| chr21:31723321
|
G | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+8342C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723321 | ||||||
| chr21:31723452
|
C | CA | 21 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0151others(18): Show | 21 | HG00099.hp1 HG01071.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+8210dupT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723452 | ||||||
| chr21:31723471
|
CAAACAAA others(5): Show |
C | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+8180_30+8191del others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723471 | ||||||
| chr21:31723481
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.30+8182T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723481 | ||||||
| chr21:31723502
|
T | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(121): Show | 127 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.30+8161A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723502 | ||||||
| chr21:31723609
|
G | GTT | 21 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(18): Show | 22 | HG00621.hp1 HG01243.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.30+8053_30+8054ins others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723609 | ||||||
| chr21:31723609
|
G | GTTGT | 52 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0039others(49): Show | 52 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.30+8053_30+8054ins others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723609 | ||||||
| chr21:31723609
|
G | GTTGTGT | 9 | a0001c0001t0001g0015a0001c0001t0001g0084a0001c0001t0001g0085others(6): Show | 10 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+8053_30+8054ins others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723609 | ||||||
| chr21:31723609
|
G | GTTGTGTG others(5): Show |
5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+8053_30+8054ins others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723609 | ||||||
| chr21:31723610
|
A | ATG | 13 | a0001c0001t0001g0133a0001c0001t0001g0151a0001c0001t0001g0152others(10): Show | 13 | HG00741.hp2 HG01070.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+8051_30+8052dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723610 | ||||||
| chr21:31723610
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(85): Show | 91 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.30+8053T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723610 | ||||||
| chr21:31723610
|
A | T | 37 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0086others(34): Show | 37 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.30+8053T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723610 | ||||||
| chr21:31723627
|
T | C | 2 | a0001c0001t0001g0307a0002c0006t0001g0308 | 2 | HG01257.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.30+8036A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723627 | ||||||
| chr21:31723627
|
T | TGC | 9 | a0001c0001t0001g0225a0001c0001t0001g0303a0001c0001t0001g0304others(6): Show | 9 | HG00642.hp2 HG01168.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+8035_30+8036ins others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723627 | ||||||
| chr21:31723627
|
T | TGCGC | 8 | a0001c0001t0001g0242a0001c0001t0001g0309a0001c0001t0001g0310others(5): Show | 8 | HG01261.hp1 HG01358.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+8035_30+8036ins others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723627 | ||||||
| chr21:31723629
|
T | C | 25 | a0001c0001t0001g0225a0001c0001t0001g0242a0001c0001t0001g0273others(22): Show | 25 | HG00642.hp2 HG01081.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.30+8034A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | ||||||
| chr21:31723629
|
T | TGC | 56 | a0001c0001t0001g0086a0001c0001t0001g0117a0001c0001t0001g0131others(53): Show | 56 | HG00140.hp1 HG00642.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.30+8032_30+8033dup others(2): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | ||||||
| chr21:31723629
|
T | TGCGC | 29 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0280others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.30+8030_30+8033dup others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | ||||||
| chr21:31723629
|
T | TGTGC | 12 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(9): Show | 12 | HG01433.hp1 HG02040.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+8033_30+8034ins others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | ||||||
| chr21:31723629
|
T | TGTGCGC | 8 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0238others(5): Show | 8 | HG01074.hp2 HG02040.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+8033_30+8034ins others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | ||||||
| chr21:31723629
|
T | TGTGTGC | 12 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(9): Show | 12 | HG00408.hp2 HG00544.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+8033_30+8034ins others(6): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | ||||||
| chr21:31723629
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0320 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.30+8033_30+8034ins others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | ||||||
| chr21:31723629
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0001g0321 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.30+8033_30+8034ins others(12): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | ||||||
| chr21:31723629
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+8033_30+8034ins others(10): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | ||||||
| chr21:31723629
|
T | TGTGTGTG others(15): Show |
1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+8033_30+8034ins others(22): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | ||||||
| chr21:31723629
|
TGCGC | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0318a0001c0001t0001g0319others(17): Show | 21 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+8030_30+8033del others(4): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723629 | ||||||
| chr21:31723631
|
C | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0104others(15): Show | 20 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.30+8032G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723631 | ||||||
| chr21:31723633
|
C | T | 4 | a0001c0001t0001g0020a0001c0005t0001g0345a0001c0005t0002g0343others(1): Show | 4 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+8030G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723633 | ||||||
| chr21:31723635
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0318a0001c0001t0001g0319others(17): Show | 21 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+8028G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723635 | ||||||
| chr21:31723638
|
G | A | 4 | a0001c0001t0003g0327a0001c0001t0003g0331a0001c0001t0003g0332others(1): Show | 4 | HG03017.hp2 HG03239.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+8025C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723638 | ||||||
| chr21:31723638
|
G | T | 1 | a0001c0002t0002g0139 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.30+8025C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723638 | ||||||
| chr21:31723646
|
G | A | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+8017C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723646 | ||||||
| chr21:31723790
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 10 | HG00738.hp1 HG01099.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+7873G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723790 | ||||||
| chr21:31723805
|
G | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+7858C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723805 | ||||||
| chr21:31723821
|
A | G | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+7842T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723821 | ||||||
| chr21:31723886
|
T | C | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+7777A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31723886 | ||||||
| chr21:31724033
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.30+7630A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724033 | ||||||
| chr21:31724239
|
A | ACACAGAA others(105): Show |
2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | NA18943.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.30+7423_30+7424ins others(112): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724239 | ||||||
| chr21:31724249
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+7414C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724249 | ||||||
| chr21:31724285
|
G | T | 3 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340 | 3 | HG00099.hp2 HG01433.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.30+7378C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724285 | ||||||
| chr21:31724301
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.30+7362G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724301 | ||||||
| chr21:31724501
|
T | G | 1 | a0001c0001t0001g0316 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.30+7162A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724501 | ||||||
| chr21:31724552
|
G | T | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+7111C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724552 | ||||||
| chr21:31724554
|
T | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(119): Show | 125 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.30+7109A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724554 | ||||||
| chr21:31724580
|
T | C | 1 | a0001c0002t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.30+7083A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724580 | ||||||
| chr21:31724665
|
C | T | 1 | a0001c0001t0003g0327 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.30+6998G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724665 | ||||||
| chr21:31724740
|
A | C | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG00423.hp2 HG02074.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.30+6923T>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724740 | ||||||
| chr21:31724765
|
T | A | 1 | a0001c0001t0002g0103 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.30+6898A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724765 | ||||||
| chr21:31724896
|
G | C | 1 | a0001c0001t0001g0317 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.30+6767C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31724896 | ||||||
| chr21:31725198
|
C | A | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+6465G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725198 | ||||||
| chr21:31725345
|
T | C | 1 | a0001c0002t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.30+6318A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725345 | ||||||
| chr21:31725443
|
C | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+6220G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725443 | ||||||
| chr21:31725723
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+5940A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725723 | ||||||
| chr21:31725761
|
C | T | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(119): Show | 125 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.30+5902G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725761 | ||||||
| chr21:31725849
|
C | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5814G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725849 | ||||||
| chr21:31725879
|
C | T | 3 | a0001c0004t0001g0009a0001c0004t0001g0010a0001c0004t0001g0011 | 3 | HG01175.hp2 HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.30+5784G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725879 | ||||||
| chr21:31725884
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5779G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725884 | ||||||
| chr21:31725889
|
C | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5774G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725889 | ||||||
| chr21:31725891
|
T | A | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.30+5772A>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31725891 | ||||||
| chr21:31726098
|
T | C | 1 | a0001c0002t0001g0228 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.30+5565A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726098 | ||||||
| chr21:31726191
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5472C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726191 | ||||||
| chr21:31726199
|
C | A | 1 | a0001c0001t0001g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+5464G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726199 | ||||||
| chr21:31726208
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.30+5455C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726208 | ||||||
| chr21:31726236
|
G | A | 1 | a0001c0002t0007g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.30+5427C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726236 | ||||||
| chr21:31726236
|
G | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5427C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726236 | ||||||
| chr21:31726302
|
C | G | 1 | a0001c0001t0006g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.30+5361G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726302 | ||||||
| chr21:31726344
|
G | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0318a0001c0001t0001g0319others(20): Show | 24 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.30+5319C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726344 | ||||||
| chr21:31726552
|
C | T | 1 | a0001c0003t0002g0016 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.30+5111G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726552 | ||||||
| chr21:31726555
|
C | T | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+5108G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726555 | ||||||
| chr21:31726565
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.30+5098A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726565 | ||||||
| chr21:31726596
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 7 | HG02615.hp2 HG02965.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+5067G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726596 | ||||||
| chr21:31726724
|
T | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 6 | HG02615.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+4939A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726724 | ||||||
| chr21:31726855
|
G | A | 9 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(6): Show | 9 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+4808C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726855 | ||||||
| chr21:31726892
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.30+4771T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31726892 | ||||||
| chr21:31727076
|
G | C | 1 | a0001c0001t0001g0116 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.30+4587C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727076 | ||||||
| chr21:31727079
|
CT | C | 9 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(6): Show | 9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+4583delA | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727079 | ||||||
| chr21:31727136
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.30+4527A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727136 | ||||||
| chr21:31727155
|
T | G | 4 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(1): Show | 4 | HG00099.hp2 HG01433.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+4508A>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727155 | ||||||
| chr21:31727415
|
T | C | 1 | a0001c0002t0001g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+4248A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727415 | ||||||
| chr21:31727535
|
G | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+4128C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727535 | ||||||
| chr21:31727655
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.30+4008C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727655 | ||||||
| chr21:31727696
|
C | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+3967G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727696 | ||||||
| chr21:31727913
|
A | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+3750T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727913 | ||||||
| chr21:31727932
|
CA | C | 346 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(343): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.30+3730delT | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31727932 | ||||||
| chr21:31728194
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.30+3469C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728194 | ||||||
| chr21:31728482
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG03491.hp1 HG03492.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+3181G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728482 | ||||||
| chr21:31728487
|
A | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(120): Show | 126 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.30+3176T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728487 | ||||||
| chr21:31728561
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(120): Show | 126 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.30+3102G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728561 | ||||||
| chr21:31728657
|
A | G | 7 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(4): Show | 7 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+3006T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728657 | ||||||
| chr21:31728658
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.30+3005A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728658 | ||||||
| chr21:31728844
|
T | C | 1 | a0001c0007t0001g0323 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.30+2819A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31728844 | ||||||
| chr21:31729020
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG02109.hp1 HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.30+2643G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729020 | ||||||
| chr21:31729267
|
C | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2396G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729267 | ||||||
| chr21:31729274
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+2389G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729274 | ||||||
| chr21:31729486
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.30+2177C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729486 | ||||||
| chr21:31729567
|
G | C | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2096C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729567 | ||||||
| chr21:31729568
|
G | C | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2095C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729568 | ||||||
| chr21:31729569
|
G | C | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2094C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729569 | ||||||
| chr21:31729570
|
G | C | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2093C>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729570 | ||||||
| chr21:31729572
|
A | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2091T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729572 | ||||||
| chr21:31729573
|
C | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2090G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729573 | ||||||
| chr21:31729574
|
G | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2089C>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729574 | ||||||
| chr21:31729579
|
A | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2084T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729579 | ||||||
| chr21:31729580
|
A | T | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+2083T>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729580 | ||||||
| chr21:31729686
|
T | C | 109 | a0001c0001t0001g0005a0001c0001t0001g0236a0001c0001t0001g0237others(106): Show | 110 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.30+1977A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729686 | ||||||
| chr21:31729691
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.30+1972T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729691 | ||||||
| chr21:31729695
|
G | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+1968C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729695 | ||||||
| chr21:31729763
|
T | C | 1 | a0001c0001t0002g0324 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.30+1900A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729763 | ||||||
| chr21:31729780
|
T | C | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+1883A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31729780 | ||||||
| chr21:31730415
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(121): Show | 127 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.30+1248G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730415 | ||||||
| chr21:31730423
|
A | G | 9 | a0001c0003t0001g0118a0001c0003t0001g0119a0001c0003t0001g0120others(6): Show | 9 | HG01952.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+1240T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730423 | ||||||
| chr21:31730496
|
C | A | 1 | a0001c0011t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+1167G>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730496 | ||||||
| chr21:31730498
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(103): Show | 108 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.30+1165T>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730498 | ||||||
| chr21:31730751
|
T | C | 1 | a0002c0006t0001g0326 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.30+912A>G | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730751 | ||||||
| chr21:31730845
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0328a0001c0001t0001g0329others(15): Show | 19 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+818C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730845 | ||||||
| chr21:31730866
|
C | T | 2 | a0001c0002t0001g0013a0001c0002t0001g0014 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.30+797G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730866 | ||||||
| chr21:31730927
|
A | ACAACGCC others(6): Show |
1 | a0001c0002t0001g0012 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.30+723_30+735dupAA others(11): Show |
SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31730927 | ||||||
| chr21:31731259
|
C | T | 3 | a0001c0004t0001g0009a0001c0004t0001g0010a0001c0004t0001g0011 | 3 | HG01175.hp2 HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.30+404G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31731259 | ||||||
| chr21:31731307
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.30+356C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31731307 | ||||||
| chr21:31731336
|
G | A | 3 | a0001c0005t0001g0345a0001c0005t0002g0343a0001c0005t0002g0344 | 3 | HG00738.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.30+327C>T | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31731336 | ||||||
| chr21:31731381
|
C | G | 2 | a0001c0001t0003g0007a0001c0001t0003g0008 | 2 | HG00639.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.30+282G>C | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31731381 | ||||||
| chr21:31731638
|
C | T | 1 | a0001c0001t0004g0006 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.30+25G>A | SCAF4 | ENSG00000156304.15 | transcript | ENST00000286835.12 | protein_coding | 1/19 | chr21 | 31731638 |