| geneid | 51322 |
|---|---|
| ensemblid | ENSG00000095787.26 |
| hgncid | 17327 |
| symbol | WAC |
| name | WW domain containing adaptor with coiled-coil |
| refseq_nuc | NM_016628.5 |
| refseq_prot | NP_057712.2 |
| ensembl_nuc | ENST00000354911.9 |
| ensembl_prot | ENSP00000346986.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 28533118 |
| end | 28623112 |
| strand | + |
| ver | v1.2 |
| region | chr10:28533118-28623112 |
| region5000 | chr10:28528118-28628112 |
| regionname0 | WAC_chr10_28533118_28623112 |
| regionname5000 | WAC_chr10_28528118_28628112 |
| 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 | 647 | 317 | 83 | 67 | 126 | 12 | 27 | 88 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0002 | 0/0 | 647 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0003 | 0/0 | 647 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| 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 | 1944 | 302 | 71 | 65 | 126 | 12 | 26 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| c0002 | 0/0 | 1944 | 10 | 9 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| c0003 | 0/0 | 1944 | 4 | 3 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| c0004 | 0/0 | 1944 | 3 | 2 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| c0005 | 0/0 | 1944 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| c0006 | 0/0 | 1944 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| c0007 | 0/0 | 1944 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3968 | 16 | 5 | 4 | 5 | 0 | 2 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0002 | 0/0 | 3965 | 14 | 3 | 3 | 5 | 0 | 3 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0003 | 0/0 | 3967 | 10 | 1 | 0 | 6 | 0 | 3 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0004 | 0/0 | 3968 | 10 | 0 | 3 | 6 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0005 | 0/0 | 3969 | 9 | 3 | 5 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0006 | 0/0 | 3964 | 9 | 2 | 4 | 2 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0007 | 0/1 | 3969 | 8 | 1 | 0 | 6 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0008 | 0/0 | 3966 | 8 | 0 | 2 | 4 | 1 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0009 | 0/0 | 3966 | 7 | 2 | 2 | 3 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0010 | 0/0 | 3968 | 7 | 0 | 0 | 6 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0011 | 0/0 | 3968 | 7 | 0 | 3 | 2 | 0 | 2 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0012 | 0/0 | 3967 | 6 | 3 | 0 | 0 | 2 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0013 | 0/0 | 3962 | 6 | 6 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0014 | 0/0 | 3971 | 5 | 2 | 1 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0015 | 0/0 | 3967 | 5 | 0 | 2 | 3 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0016 | 0/0 | 3969 | 4 | 0 | 0 | 4 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0017 | 0/0 | 3967 | 4 | 0 | 3 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0018 | 0/0 | 3972 | 4 | 0 | 3 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0019 | 0/0 | 3970 | 4 | 0 | 2 | 0 | 0 | 2 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0020 | 0/0 | 3969 | 4 | 1 | 0 | 2 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0021 | 0/0 | 3965 | 4 | 2 | 2 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0022 | 0/0 | 3963 | 4 | 3 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0023 | 0/0 | 3963 | 3 | 3 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0024 | 0/0 | 3972 | 3 | 0 | 1 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0025 | 0/0 | 3967 | 3 | 1 | 0 | 0 | 0 | 2 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0026 | 0/0 | 3968 | 3 | 3 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0027 | 0/0 | 3966 | 3 | 3 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0028 | 0/0 | 3966 | 3 | 2 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0029 | 0/0 | 3966 | 2 | 0 | 2 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0030 | 0/0 | 3970 | 2 | 0 | 0 | 1 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0031 | 0/0 | 3963 | 2 | 1 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0032 | 0/0 | 3966 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0033 | 0/0 | 3968 | 2 | 1 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0034 | 0/0 | 3966 | 2 | 0 | 2 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0035 | 0/0 | 3960 | 2 | 2 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0036 | 0/0 | 3970 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0037 | 0/0 | 3971 | 2 | 0 | 1 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0038 | 0/0 | 3969 | 2 | 0 | 1 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0039 | 0/0 | 3970 | 2 | 2 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0040 | 0/0 | 3970 | 2 | 2 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0041 | 0/0 | 3967 | 2 | 1 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0042 | 0/0 | 3964 | 2 | 2 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0043 | 0/0 | 3970 | 2 | 0 | 0 | 1 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0044 | 0/0 | 3967 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0045 | 0/0 | 3965 | 2 | 0 | 0 | 1 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0046 | 0/0 | 3971 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0047 | 0/0 | 3970 | 2 | 0 | 1 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0048 | 0/0 | 3967 | 2 | 0 | 1 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0049 | 0/0 | 3965 | 2 | 0 | 0 | 1 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0050 | 0/0 | 3964 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0051 | 1/0 | 3969 | 1 | 0 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0052 | 0/0 | 3968 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0053 | 0/0 | 3970 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0054 | 0/0 | 3968 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0055 | 0/0 | 3971 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0056 | 0/0 | 3960 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0057 | 0/0 | 3968 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0058 | 0/0 | 3967 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0059 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0060 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0061 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0062 | 0/0 | 3972 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0063 | 0/0 | 3971 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0064 | 0/0 | 3970 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0065 | 0/0 | 3968 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0066 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0067 | 0/0 | 3968 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0068 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0069 | 0/0 | 3954 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0070 | 0/0 | 3968 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0071 | 0/0 | 3968 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0072 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0073 | 0/0 | 3967 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0074 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0075 | 0/0 | 3966 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0076 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0077 | 0/0 | 3962 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0078 | 0/0 | 3955 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0079 | 0/0 | 3955 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0080 | 0/0 | 3967 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0081 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0082 | 0/0 | 3972 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0083 | 0/0 | 3971 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0084 | 0/0 | 3969 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0085 | 0/0 | 3968 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0086 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0087 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0088 | 0/0 | 3971 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0089 | 0/0 | 3969 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0090 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0091 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0092 | 0/0 | 3968 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0093 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0094 | 0/0 | 3966 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0095 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0096 | 0/0 | 3959 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0097 | 0/0 | 3966 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0098 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0099 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0100 | 0/0 | 3966 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0101 | 0/0 | 3971 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0102 | 0/0 | 3967 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0103 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0104 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0105 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0106 | 0/0 | 3968 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0107 | 0/0 | 3969 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0108 | 0/0 | 3968 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0109 | 0/0 | 3962 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0110 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0111 | 0/0 | 3970 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0112 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0113 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0114 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0115 | 0/0 | 3968 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0116 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0117 | 0/0 | 3971 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0118 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0119 | 0/0 | 3968 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0120 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0121 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0122 | 0/0 | 3968 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0123 | 0/0 | 3968 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0124 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0125 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0126 | 0/0 | 3969 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0127 | 0/0 | 3966 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0128 | 0/0 | 3969 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0129 | 0/0 | 3961 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0130 | 0/0 | 3968 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0131 | 0/0 | 3966 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0132 | 0/0 | 3967 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0133 | 0/0 | 3968 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0134 | 0/0 | 3968 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0135 | 0/0 | 3978 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0136 | 0/0 | 3966 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0137 | 0/0 | 3966 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0138 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0139 | 0/0 | 3976 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0140 | 0/0 | 3971 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0141 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0142 | 0/0 | 3967 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0143 | 0/0 | 3969 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0144 | 0/0 | 3967 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0145 | 0/0 | 3966 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0146 | 0/0 | 3965 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0147 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0148 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0149 | 0/0 | 3971 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0150 | 0/0 | 3970 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0151 | 0/0 | 3966 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0152 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0153 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0154 | 0/0 | 3966 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| t0155 | 0/0 | 3968 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| 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 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| 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 | 1944 | 302 | 71 | 65 | 126 | 12 | 26 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0002 | 0/0 | 1944 | 10 | 9 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0004 | 0/0 | 1944 | 3 | 2 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0005 | 0/0 | 1944 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0007 | 0/0 | 1944 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0002c0003 | 0/0 | 1944 | 4 | 3 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0003c0006 | 0/0 | 1944 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5911 | 16 | 5 | 4 | 5 | 0 | 2 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0002 | 0/0 | 5908 | 14 | 3 | 3 | 5 | 0 | 3 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0003 | 0/0 | 5910 | 10 | 1 | 0 | 6 | 0 | 3 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0004 | 0/0 | 5911 | 10 | 0 | 3 | 6 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0005 | 0/0 | 5912 | 9 | 3 | 5 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0006 | 0/0 | 5907 | 9 | 2 | 4 | 2 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0007 | 0/1 | 5912 | 8 | 1 | 0 | 6 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0008 | 0/0 | 5909 | 8 | 0 | 2 | 4 | 1 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0009 | 0/0 | 5909 | 7 | 2 | 2 | 3 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0010 | 0/0 | 5911 | 7 | 0 | 0 | 6 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0011 | 0/0 | 5911 | 7 | 0 | 3 | 2 | 0 | 2 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0012 | 0/0 | 5910 | 6 | 3 | 0 | 0 | 2 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0014 | 0/0 | 5914 | 5 | 2 | 1 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0015 | 0/0 | 5910 | 5 | 0 | 2 | 3 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0016 | 0/0 | 5912 | 4 | 0 | 0 | 4 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0017 | 0/0 | 5910 | 4 | 0 | 3 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0018 | 0/0 | 5915 | 4 | 0 | 3 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0019 | 0/0 | 5913 | 3 | 0 | 2 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0020 | 0/0 | 5912 | 3 | 1 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0021 | 0/0 | 5908 | 4 | 2 | 2 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0022 | 0/0 | 5906 | 4 | 3 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0023 | 0/0 | 5906 | 3 | 3 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0024 | 0/0 | 5915 | 3 | 0 | 1 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0025 | 0/0 | 5910 | 3 | 1 | 0 | 0 | 0 | 2 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0026 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0027 | 0/0 | 5909 | 3 | 3 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0028 | 0/0 | 5909 | 3 | 2 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0029 | 0/0 | 5909 | 2 | 0 | 2 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0030 | 0/0 | 5913 | 2 | 0 | 0 | 1 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0031 | 0/0 | 5906 | 2 | 1 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0032 | 0/0 | 5909 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0033 | 0/0 | 5911 | 2 | 1 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0034 | 0/0 | 5909 | 2 | 0 | 2 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0036 | 0/0 | 5913 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0037 | 0/0 | 5914 | 2 | 0 | 1 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0038 | 0/0 | 5912 | 2 | 0 | 1 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0039 | 0/0 | 5913 | 2 | 2 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0040 | 0/0 | 5913 | 2 | 2 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0042 | 0/0 | 5907 | 2 | 2 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0043 | 0/0 | 5913 | 2 | 0 | 0 | 1 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0044 | 0/0 | 5910 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0045 | 0/0 | 5908 | 2 | 0 | 0 | 1 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0046 | 0/0 | 5914 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0047 | 0/0 | 5913 | 2 | 0 | 1 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0048 | 0/0 | 5910 | 2 | 0 | 1 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0049 | 0/0 | 5908 | 2 | 0 | 0 | 1 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0050 | 0/0 | 5907 | 2 | 0 | 0 | 2 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0051 | 1/0 | 5912 | 1 | 0 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0052 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0053 | 0/0 | 5913 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0054 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0055 | 0/0 | 5914 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0056 | 0/0 | 5903 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0057 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0058 | 0/0 | 5910 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0059 | 0/0 | 5910 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0060 | 0/0 | 5915 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0061 | 0/0 | 5915 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0062 | 0/0 | 5915 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0063 | 0/0 | 5914 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0064 | 0/0 | 5913 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0065 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0066 | 0/0 | 5906 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0067 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0068 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0070 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0071 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0073 | 0/0 | 5910 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0074 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0075 | 0/0 | 5909 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0076 | 0/0 | 5906 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0077 | 0/0 | 5905 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0080 | 0/0 | 5910 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0081 | 0/0 | 5906 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0082 | 0/0 | 5915 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0083 | 0/0 | 5914 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0084 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0085 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0086 | 0/0 | 5908 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0087 | 0/0 | 5907 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0088 | 0/0 | 5914 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0089 | 0/0 | 5912 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0091 | 0/0 | 5916 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0092 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0093 | 0/0 | 5910 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0094 | 0/0 | 5909 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0095 | 0/0 | 5908 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0097 | 0/0 | 5909 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0098 | 0/0 | 5907 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0099 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0100 | 0/0 | 5909 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0101 | 0/0 | 5914 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0102 | 0/0 | 5910 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0103 | 0/0 | 5908 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0104 | 0/0 | 5908 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0105 | 0/0 | 5916 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0106 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0107 | 0/0 | 5912 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0108 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0109 | 0/0 | 5905 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0110 | 0/0 | 5910 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0111 | 0/0 | 5913 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0112 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0113 | 0/0 | 5906 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0114 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0115 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0116 | 0/0 | 5907 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0117 | 0/0 | 5914 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0118 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0119 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0120 | 0/0 | 5906 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0121 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0122 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0123 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0124 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0125 | 0/0 | 5908 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0126 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0127 | 0/0 | 5909 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0128 | 0/0 | 5912 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0129 | 0/0 | 5904 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0130 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0131 | 0/0 | 5909 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0132 | 0/0 | 5910 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0133 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0134 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0135 | 0/0 | 5921 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0136 | 0/0 | 5909 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0137 | 0/0 | 5909 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0138 | 0/0 | 5908 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0139 | 0/0 | 5919 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0140 | 0/0 | 5914 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0141 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0142 | 0/0 | 5910 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0143 | 0/0 | 5912 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0144 | 0/0 | 5910 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0145 | 0/0 | 5909 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0146 | 0/0 | 5908 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0147 | 0/0 | 5907 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0148 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0149 | 0/0 | 5914 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0150 | 0/0 | 5913 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0151 | 0/0 | 5909 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0152 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0153 | 0/0 | 5906 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0154 | 0/0 | 5909 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0001t0155 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0002t0013 | 0/0 | 5905 | 6 | 6 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0002t0035 | 0/0 | 5903 | 2 | 2 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0002t0072 | 0/0 | 5908 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0002t0096 | 0/0 | 5902 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0004t0069 | 0/0 | 5897 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0004t0078 | 0/0 | 5898 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0004t0079 | 0/0 | 5898 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0005t0090 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0001c0007t0019 | 0/0 | 5913 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0002c0003t0026 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0002c0003t0041 | 0/0 | 5910 | 2 | 1 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| a0003c0006t0020 | 0/0 | 5912 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | copy fasta | chr10 | 28528118 | 28628112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0007g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0008g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0009g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0009g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0009g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0009g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0009g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0010g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0011g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0012g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0012g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0012g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0012g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0012g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0014g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0014g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0014g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0014g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0014g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0015g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0015g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0015g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0015g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0015g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0016g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0016g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0016g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0016g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0017g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0017g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0017g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0017g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0018g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0018g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0018g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0018g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0019g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0019g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0019g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0020g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0020g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0020g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0021g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0021g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0021g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0021g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0022g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0022g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0022g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0022g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0023g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0023g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0023g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0024g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0024g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0024g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0025g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0025g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0025g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0026g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0027g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0027g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0027g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0028g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0028g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0028g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0029g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0029g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0030g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0030g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0031g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0031g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0032g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0032g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0033g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0033g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0034g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0034g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0036g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0036g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0037g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0037g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0038g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0038g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0039g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0039g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0040g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0040g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0042g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0042g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0043g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0043g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0044g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0044g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0045g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0045g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0046g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0046g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0047g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0047g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0048g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0048g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0049g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0049g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0050g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0050g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0051g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0052g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0053g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0054g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0055g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0056g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0057g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0058g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0059g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0060g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0061g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0062g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0063g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0064g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0065g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0066g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0067g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0068g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0070g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0071g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0073g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0074g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0075g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0076g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0077g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0080g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0081g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0082g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0083g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0084g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0085g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0086g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0087g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0088g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0089g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0091g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0092g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0093g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0094g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0095g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0097g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0098g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0099g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0100g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0101g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0102g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0103g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0104g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0105g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0106g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0107g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0108g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0109g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0110g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0111g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0112g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0113g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0114g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0115g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0116g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0117g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0118g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0119g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0120g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0121g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0122g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0123g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0124g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0125g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0126g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0127g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0128g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0129g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0130g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0131g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0132g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0133g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0134g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0135g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0136g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0137g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0138g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0139g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0140g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0141g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0142g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0143g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0144g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0145g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0146g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0147g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0148g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0149g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0150g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0151g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0152g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0153g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0154g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0001t0155g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0013g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0013g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0013g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0013g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0013g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0035g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0035g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0072g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0002t0096g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0004t0069g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0004t0078g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0004t0079g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0005t0090g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0001c0007t0019g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0002c0003t0026g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0002c0003t0026g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0002c0003t0041g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0002c0003t0041g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| a0003c0006t0020g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0008 | g0048 | EUR | GBR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00099 | hp2 | a0001 | c0001 | t0043 | g0276 | EUR | GBR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00140 | hp1 | a0001 | c0001 | t0073 | g0137 | EUR | GBR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00140 | hp2 | a0001 | c0001 | t0089 | g0264 | EUR | GBR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00280 | hp1 | a0001 | c0001 | t0045 | g0012 | EUR | FIN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00280 | hp2 | a0001 | c0001 | t0012 | g0277 | EUR | FIN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00323 | hp1 | a0001 | c0001 | t0012 | g0265 | EUR | FIN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00323 | hp2 | a0001 | c0001 | t0146 | g0047 | EUR | FIN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00438 | hp1 | a0001 | c0001 | t0009 | g0319 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00438 | hp2 | a0001 | c0001 | t0065 | g0225 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00558 | hp2 | a0001 | c0001 | t0011 | g0241 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00609 | hp1 | a0001 | c0001 | t0043 | g0289 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00609 | hp2 | a0001 | c0001 | t0050 | g0018 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0062 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00621 | hp2 | a0001 | c0001 | t0124 | g0250 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00639 | hp1 | a0001 | c0001 | t0058 | g0310 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0069 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0156 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00673 | hp1 | a0001 | c0001 | t0130 | g0043 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00673 | hp2 | a0001 | c0001 | t0097 | g0135 | EAS | CHS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00733 | hp1 | a0001 | c0001 | t0038 | g0248 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00733 | hp2 | a0001 | c0001 | t0139 | g0046 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00735 | hp1 | a0001 | c0001 | t0014 | g0215 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00735 | hp2 | a0001 | c0002 | t0096 | g0004 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00738 | hp1 | a0001 | c0001 | t0018 | g0257 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0133 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG00741 | hp2 | a0001 | c0001 | t0018 | g0278 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01069 | hp1 | a0001 | c0004 | t0069 | g0182 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01069 | hp2 | a0001 | c0001 | t0131 | g0013 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01081 | hp1 | a0001 | c0001 | t0017 | g0134 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01081 | hp2 | a0001 | c0001 | t0037 | g0251 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01099 | hp1 | a0001 | c0001 | t0018 | g0270 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01099 | hp2 | a0001 | c0001 | t0022 | g0303 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01106 | hp1 | a0001 | c0001 | t0047 | g0049 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01106 | hp2 | a0001 | c0001 | t0021 | g0304 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01109 | hp1 | a0001 | c0001 | t0015 | g0189 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01109 | hp2 | a0001 | c0001 | t0150 | g0065 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0208 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01168 | hp1 | a0001 | c0001 | t0011 | g0318 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01168 | hp2 | a0001 | c0001 | t0070 | g0275 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01175 | hp1 | a0001 | c0001 | t0029 | g0311 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01175 | hp2 | a0001 | c0001 | t0048 | g0063 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0172 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01192 | hp2 | a0001 | c0001 | t0029 | g0312 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0173 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01243 | hp2 | a0001 | c0001 | t0021 | g0300 | AMR | PUR | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01255 | hp2 | a0001 | c0001 | t0011 | g0237 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01256 | hp1 | a0001 | c0001 | t0134 | g0052 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01256 | hp2 | a0001 | c0001 | t0034 | g0260 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01257 | hp1 | a0001 | c0001 | t0133 | g0051 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01261 | hp2 | a0001 | c0001 | t0019 | g0273 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01346 | hp1 | a0001 | c0001 | t0080 | g0131 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01346 | hp2 | a0001 | c0001 | t0019 | g0267 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0116 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0249 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01361 | hp2 | a0001 | c0001 | t0067 | g0269 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01496 | hp1 | a0001 | c0001 | t0062 | g0078 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0011 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01515 | hp1 | a0001 | c0001 | t0127 | g0261 | EUR | IBS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01515 | hp2 | a0001 | c0001 | t0145 | g0050 | EUR | IBS | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01884 | hp1 | a0001 | c0001 | t0022 | g0002 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01884 | hp2 | a0001 | c0001 | t0085 | g0200 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01891 | hp1 | a0001 | c0001 | t0020 | g0238 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01891 | hp2 | a0001 | c0005 | t0090 | g0220 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01928 | hp2 | a0001 | c0001 | t0064 | g0077 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0212 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01934 | hp2 | a0001 | c0001 | t0024 | g0079 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01943 | hp1 | a0001 | c0001 | t0063 | g0105 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01975 | hp1 | a0001 | c0001 | t0017 | g0120 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01975 | hp2 | a0001 | c0001 | t0017 | g0214 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0201 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01978 | hp2 | a0001 | c0001 | t0008 | g0055 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01981 | hp1 | a0001 | c0001 | t0102 | g0280 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01981 | hp2 | a0001 | c0001 | t0034 | g0263 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02004 | hp1 | a0001 | c0001 | t0009 | g0211 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02004 | hp2 | a0001 | c0001 | t0107 | g0232 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02040 | hp1 | a0001 | c0001 | t0121 | g0262 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02040 | hp2 | a0001 | c0001 | t0083 | g0113 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02055 | hp1 | a0001 | c0004 | t0078 | g0128 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02055 | hp2 | a0001 | c0002 | t0035 | g0009 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02056 | hp1 | a0001 | c0001 | t0010 | g0272 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02056 | hp2 | a0001 | c0001 | t0009 | g0185 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02071 | hp2 | a0001 | c0001 | t0038 | g0245 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0284 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02074 | hp2 | a0001 | c0001 | t0020 | g0242 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02080 | hp1 | a0001 | c0001 | t0024 | g0099 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02083 | hp1 | a0001 | c0001 | t0054 | g0207 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02083 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02129 | hp1 | a0001 | c0001 | t0154 | g0307 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02129 | hp2 | a0001 | c0001 | t0055 | g0184 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02132 | hp1 | a0001 | c0001 | t0016 | g0143 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02132 | hp2 | a0001 | c0001 | t0147 | g0033 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02135 | hp1 | a0001 | c0001 | t0010 | g0098 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02135 | hp2 | a0001 | c0001 | t0015 | g0154 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0281 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02145 | hp2 | a0001 | c0001 | t0056 | g0255 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CDX | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02155 | hp2 | a0001 | c0001 | t0009 | g0176 | EAS | CDX | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02257 | hp2 | a0001 | c0001 | t0040 | g0228 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02273 | hp1 | a0001 | c0001 | t0143 | g0317 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02273 | hp2 | a0001 | c0001 | t0015 | g0187 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02293 | hp1 | a0001 | c0001 | t0136 | g0060 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02451 | hp2 | a0001 | c0001 | t0028 | g0290 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02523 | hp1 | a0001 | c0001 | t0099 | g0090 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02523 | hp2 | a0001 | c0001 | t0008 | g0019 | EAS | KHV | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02572 | hp1 | a0001 | c0002 | t0035 | g0103 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0203 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02622 | hp1 | a0001 | c0001 | t0042 | g0298 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0119 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02630 | hp1 | a0001 | c0002 | t0013 | g0005 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02630 | hp2 | a0001 | c0001 | t0021 | g0002 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02647 | hp1 | a0001 | c0001 | t0060 | g0136 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02647 | hp2 | a0001 | c0002 | t0013 | g0007 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02698 | hp1 | a0001 | c0001 | t0129 | g0064 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02698 | hp2 | a0001 | c0001 | t0019 | g0271 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02717 | hp1 | a0001 | c0001 | t0081 | g0071 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02717 | hp2 | a0001 | c0001 | t0077 | g0165 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02723 | hp1 | a0001 | c0001 | t0151 | g0205 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02723 | hp2 | a0002 | c0003 | t0026 | g0229 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02738 | hp2 | a0001 | c0001 | t0025 | g0224 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02809 | hp1 | a0001 | c0001 | t0148 | g0114 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02809 | hp2 | a0001 | c0002 | t0013 | g0003 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02818 | hp1 | a0001 | c0001 | t0042 | g0305 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02818 | hp2 | a0001 | c0001 | t0025 | g0244 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02886 | hp2 | a0001 | c0002 | t0013 | g0006 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02895 | hp1 | a0001 | c0001 | t0119 | g0308 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02895 | hp2 | a0001 | c0001 | t0023 | g0256 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02896 | hp1 | a0002 | c0003 | t0026 | g0068 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02896 | hp2 | a0001 | c0002 | t0013 | g0008 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02897 | hp1 | a0001 | c0001 | t0033 | g0309 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02897 | hp2 | a0001 | c0002 | t0072 | g0010 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02922 | hp1 | a0001 | c0001 | t0094 | g0167 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02922 | hp2 | a0001 | c0001 | t0110 | g0295 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02965 | hp1 | a0001 | c0001 | t0120 | g0104 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02965 | hp2 | a0001 | c0001 | t0027 | g0294 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02970 | hp1 | a0001 | c0001 | t0109 | g0299 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02970 | hp2 | a0001 | c0001 | t0059 | g0106 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02976 | hp2 | a0001 | c0001 | t0039 | g0252 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03017 | hp2 | a0001 | c0001 | t0155 | g0159 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03041 | hp1 | a0001 | c0001 | t0104 | g0306 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03041 | hp2 | a0001 | c0001 | t0126 | g0226 | AFR | GWD | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03098 | hp1 | a0001 | c0001 | t0061 | g0268 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03098 | hp2 | a0001 | c0001 | t0108 | g0301 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0110 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03130 | hp2 | a0001 | c0001 | t0074 | g0164 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0196 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03139 | hp2 | a0001 | c0001 | t0022 | g0293 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03209 | hp1 | a0001 | c0001 | t0093 | g0178 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03209 | hp2 | a0001 | c0001 | t0039 | g0234 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03239 | hp1 | a0001 | c0001 | t0025 | g0233 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03239 | hp2 | a0001 | c0001 | t0057 | g0139 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03453 | hp1 | a0001 | c0001 | t0014 | g0111 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03453 | hp2 | a0001 | c0001 | t0026 | g0231 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03486 | hp1 | a0001 | c0001 | t0022 | g0302 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03486 | hp2 | a0001 | c0001 | t0153 | g0117 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03516 | hp2 | a0001 | c0001 | t0027 | g0296 | AFR | ESN | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03704 | hp2 | a0001 | c0001 | t0033 | g0258 | SAS | PJL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03831 | hp1 | a0001 | c0001 | t0049 | g0039 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03831 | hp2 | a0001 | c0001 | t0030 | g0218 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03834 | hp1 | a0001 | c0001 | t0010 | g0073 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03834 | hp2 | a0001 | c0007 | t0019 | g0259 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03927 | hp1 | a0001 | c0001 | t0149 | g0291 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03927 | hp2 | a0001 | c0001 | t0018 | g0283 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04115 | hp1 | a0001 | c0001 | t0011 | g0235 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04115 | hp2 | a0001 | c0001 | t0008 | g0037 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04184 | hp1 | a0001 | c0001 | t0011 | g0243 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0101 | SAS | BEB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0092 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04204 | hp1 | a0001 | c0001 | t0128 | g0015 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04228 | hp1 | a0003 | c0006 | t0020 | g0239 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18522 | hp1 | a0001 | c0001 | t0084 | g0177 | AFR | YRI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0191 | AFR | YRI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18612 | hp1 | a0001 | c0001 | t0082 | g0147 | EAS | CHB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18612 | hp2 | a0001 | c0001 | t0125 | g0246 | EAS | CHB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18747 | hp1 | a0001 | c0001 | t0016 | g0142 | EAS | CHB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | CHB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18906 | hp1 | a0001 | c0002 | t0013 | g0074 | AFR | YRI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18906 | hp2 | a0001 | c0001 | t0105 | g0253 | AFR | YRI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18940 | hp1 | a0001 | c0001 | t0028 | g0285 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18941 | hp1 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18941 | hp2 | a0001 | c0001 | t0116 | g0192 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18943 | hp1 | a0001 | c0001 | t0024 | g0086 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18943 | hp2 | a0001 | c0001 | t0049 | g0061 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18947 | hp1 | a0001 | c0001 | t0101 | g0075 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18947 | hp2 | a0001 | c0001 | t0014 | g0188 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18948 | hp1 | a0001 | c0001 | t0048 | g0020 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18948 | hp2 | a0001 | c0001 | t0112 | g0163 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18952 | hp1 | a0001 | c0001 | t0036 | g0082 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18952 | hp2 | a0001 | c0001 | t0032 | g0216 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18954 | hp1 | a0001 | c0001 | t0010 | g0081 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18954 | hp2 | a0001 | c0001 | t0032 | g0145 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18959 | hp1 | a0001 | c0001 | t0141 | g0021 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18960 | hp1 | a0001 | c0001 | t0115 | g0152 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18962 | hp1 | a0001 | c0001 | t0045 | g0028 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18964 | hp1 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18964 | hp2 | a0001 | c0001 | t0016 | g0141 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18965 | hp1 | a0001 | c0001 | t0086 | g0209 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18965 | hp2 | a0001 | c0001 | t0044 | g0095 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18967 | hp1 | a0001 | c0001 | t0046 | g0315 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18969 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18971 | hp1 | a0001 | c0001 | t0010 | g0080 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18971 | hp2 | a0001 | c0001 | t0030 | g0149 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18972 | hp1 | a0001 | c0001 | t0016 | g0183 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18975 | hp1 | a0001 | c0001 | t0068 | g0155 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18978 | hp2 | a0001 | c0001 | t0138 | g0032 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18983 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18984 | hp2 | a0001 | c0001 | t0010 | g0096 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18988 | hp1 | a0001 | c0001 | t0007 | g0023 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18988 | hp2 | a0001 | c0001 | t0132 | g0112 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18989 | hp1 | a0001 | c0001 | t0036 | g0102 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18989 | hp2 | a0001 | c0001 | t0087 | g0150 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18990 | hp1 | a0001 | c0001 | t0098 | g0157 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18990 | hp2 | a0001 | c0001 | t0122 | g0094 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18992 | hp1 | a0001 | c0001 | t0144 | g0053 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18992 | hp2 | a0001 | c0001 | t0100 | g0320 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18994 | hp1 | a0001 | c0001 | t0140 | g0056 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18994 | hp2 | a0001 | c0001 | t0015 | g0198 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18995 | hp1 | a0001 | c0001 | t0091 | g0179 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18995 | hp2 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18998 | hp1 | a0001 | c0001 | t0103 | g0194 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18998 | hp2 | a0001 | c0001 | t0047 | g0316 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0313 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19002 | hp1 | a0001 | c0001 | t0142 | g0016 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19002 | hp2 | a0001 | c0001 | t0014 | g0072 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19003 | hp2 | a0001 | c0001 | t0118 | g0287 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19005 | hp1 | a0001 | c0001 | t0010 | g0089 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19005 | hp2 | a0001 | c0001 | t0015 | g0181 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19007 | hp1 | a0001 | c0001 | t0044 | g0093 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19007 | hp2 | a0001 | c0001 | t0031 | g0125 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0121 | AFR | LWK | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0222 | AFR | LWK | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19057 | hp1 | a0001 | c0001 | t0114 | g0286 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19057 | hp2 | a0001 | c0001 | t0006 | g0122 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19058 | hp1 | a0001 | c0001 | t0046 | g0057 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19058 | hp2 | a0001 | c0001 | t0053 | g0107 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19062 | hp1 | a0001 | c0001 | t0106 | g0240 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19062 | hp2 | a0001 | c0001 | t0017 | g0190 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19068 | hp1 | a0001 | c0001 | t0095 | g0123 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19068 | hp2 | a0001 | c0001 | t0050 | g0027 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19074 | hp1 | a0001 | c0001 | t0113 | g0127 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19074 | hp2 | a0001 | c0001 | t0123 | g0088 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19077 | hp2 | a0001 | c0001 | t0037 | g0247 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19085 | hp2 | a0001 | c0001 | t0135 | g0034 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19089 | hp1 | a0001 | c0001 | t0111 | g0041 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19089 | hp2 | a0001 | c0001 | t0052 | g0066 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19090 | hp1 | a0001 | c0001 | t0092 | g0199 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19090 | hp2 | a0001 | c0001 | t0066 | g0044 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19091 | hp1 | a0001 | c0001 | t0071 | g0108 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19091 | hp2 | a0001 | c0001 | t0137 | g0038 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0221 | AFR | YRI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA19240 | hp2 | a0001 | c0001 | t0076 | g0166 | AFR | YRI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ASW | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20129 | hp2 | a0001 | c0001 | t0027 | g0297 | AFR | ASW | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | TSI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20752 | hp2 | a0001 | c0001 | t0075 | g0148 | EUR | TSI | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20905 | hp1 | a0001 | c0001 | t0012 | g0274 | SAS | GIH | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0129 | SAS | GIH | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0282 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG01123 | hp2 | a0002 | c0003 | t0041 | g0223 | AMR | CLM | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02109 | hp1 | a0001 | c0001 | t0023 | g0254 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02486 | hp1 | a0001 | c0001 | t0021 | g0292 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02486 | hp2 | a0001 | c0001 | t0088 | g0279 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG02559 | hp2 | a0001 | c0001 | t0040 | g0227 | AFR | ACB | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03471 | hp1 | a0001 | c0001 | t0152 | g0206 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG03471 | hp2 | a0001 | c0001 | t0023 | g0070 | AFR | MSL | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG06807 | hp1 | a0001 | c0001 | t0028 | g0266 | AFR | USA | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| HG06807 | hp2 | a0001 | c0004 | t0079 | g0195 | AFR | USA | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18955 | hp1 | a0001 | c0001 | t0008 | g0024 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA18955 | hp2 | a0001 | c0001 | t0117 | g0288 | EAS | JPT | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | USA | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA20300 | hp2 | a0001 | c0001 | t0031 | g0162 | AFR | USA | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | LWK | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| NA21309 | hp2 | a0002 | c0003 | t0041 | g0230 | AFR | LWK | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0059 | REF | REF | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0051 | g0236 | REF | REF | WAC_chr10_28528118_28628112 | WAC | chr10 | 28528118 | 28628112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:28608191
|
A | G | 1 | a0002 | 4 | HG01123.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.925A>G | p.Thr309Ala | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/14 | 1387/5912 | 925/1944 | 309/647 | chr10 | 28608191 | ||
| chr10:28617687
|
A | G | 1 | a0003 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1777A>G | p.Met593Val | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/14 | 2239/5912 | 1777/1944 | 593/647 | chr10 | 28617687 | ||
| chr10:28623110
|
T | G | 1 | a0001 | 1 | HG02922.hp2 | splice_region_variant | LOW | c.*3504T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | chr10 | 28623110 | ||||||
| chr10:28623110
|
TAATC | T | 1 | a0001 | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
splice_region_variant | LOW | c.*3505_*3508delAATC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | chr10 | 28623110 | ||||||
| chr10:28623112
|
A | G | 1 | a0001 | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
splice_region_variant | LOW | c.*3506A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | chr10 | 28623112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:28595923
|
A | G | 1 | a0001c0007 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.801A>G | p.Pro267Pro | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/14 | 1263/5912 | 801/1944 | 267/647 | chr10 | 28595923 | ||
| chr10:28610784
|
G | A | 1 | a0001c0005 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1251G>A | p.Thr417Thr | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/14 | 1713/5912 | 1251/1944 | 417/647 | chr10 | 28610784 | ||
| chr10:28611841
|
T | G | 1 | a0001c0004 | 3 | HG01069.hp1 HG02055.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.1356T>G | p.Ser452Ser | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/14 | 1818/5912 | 1356/1944 | 452/647 | chr10 | 28611841 | ||
| chr10:28617776
|
A | G | 1 | a0001c0002 | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
synonymous_variant | LOW | c.1866A>G | p.Arg622Arg | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/14 | 2328/5912 | 1866/1944 | 622/647 | chr10 | 28617776 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:28533160
|
A | G | 1 | a0001c0001t0155 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-420A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/14 | 420 | chr10 | 28533160 | |||||
| chr10:28533177
|
C | G | 1 | a0001c0001t0155 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-403C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/14 | 403 | chr10 | 28533177 | |||||
| chr10:28533178
|
G | A | 1 | a0001c0001t0155 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-402G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/14 | 402 | chr10 | 28533178 | |||||
| chr10:28533270
|
A | G | 1 | a0001c0001t0154 | 1 | HG02129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-310A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/14 | 310 | chr10 | 28533270 | |||||
| chr10:28533287
|
C | T | 3 | a0001c0001t0151a0001c0001t0152a0001c0001t0153 | 3 | HG02723.hp1 HG03471.hp1 HG03486.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-293C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/14 | chr10 | 28533287 | ||||||
| chr10:28533444
|
A | C | 157 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(154): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-136A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/14 | chr10 | 28533444 | ||||||
| chr10:28619710
|
T | G | 5 | a0001c0001t0016a0001c0001t0052a0001c0001t0053others(2): Show | 8 | HG02083.hp1 HG02129.hp2 HG02132.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*104T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 104 | chr10 | 28619710 | |||||
| chr10:28619734
|
C | T | 1 | a0001c0001t0150 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*128C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 128 | chr10 | 28619734 | |||||
| chr10:28619773
|
T | C | 2 | a0001c0001t0023a0001c0001t0056 | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*167T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 167 | chr10 | 28619773 | |||||
| chr10:28619813
|
G | T | 1 | a0001c0001t0149 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*207G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 207 | chr10 | 28619813 | |||||
| chr10:28619960
|
T | A | 10 | a0001c0001t0029a0001c0001t0057a0001c0001t0058others(7): Show | 11 | HG00438.hp2 HG00639.hp1 HG01175.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*354T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 354 | chr10 | 28619960 | |||||
| chr10:28619960
|
TA | T | 30 | a0001c0001t0021a0001c0001t0022a0001c0001t0023others(27): Show | 45 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*373delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 373 | INFO_REALIGN_3_PRIME | chr10 | 28619960 | ||||
| chr10:28619960
|
TAA | T | 25 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(22): Show | 54 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*372_*373delAA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 372 | INFO_REALIGN_3_PRIME | chr10 | 28619960 | ||||
| chr10:28619960
|
TAAA | T | 6 | a0001c0001t0142a0001c0001t0143a0001c0001t0144others(3): Show | 6 | HG00323.hp2 HG01515.hp2 HG02132.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*371_*373delAAA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 371 | INFO_REALIGN_3_PRIME | chr10 | 28619960 | ||||
| chr10:28619961
|
A | T | 1 | a0001c0001t0148 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*355A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 355 | chr10 | 28619961 | |||||
| chr10:28620043
|
C | T | 1 | a0001c0001t0127 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*437C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 437 | chr10 | 28620043 | |||||
| chr10:28620347
|
T | G | 1 | a0001c0001t0066 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*741T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 741 | chr10 | 28620347 | |||||
| chr10:28620370
|
GT | G | 139 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(136): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*766delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 766 | INFO_REALIGN_3_PRIME | chr10 | 28620370 | ||||
| chr10:28620454
|
T | A | 1 | a0001c0001t0066 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*848T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 848 | chr10 | 28620454 | |||||
| chr10:28620598
|
G | A | 1 | a0001c0001t0128 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*992G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 992 | chr10 | 28620598 | |||||
| chr10:28620676
|
G | A | 9 | a0001c0001t0021a0001c0001t0022a0001c0001t0023others(6): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1070G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1070 | chr10 | 28620676 | |||||
| chr10:28620716
|
A | G | 1 | a0001c0001t0066 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1110A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1110 | chr10 | 28620716 | |||||
| chr10:28620717
|
G | A | 1 | a0001c0001t0066 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1111G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1111 | chr10 | 28620717 | |||||
| chr10:28620748
|
C | A | 1 | a0001c0001t0066 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1142C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1142 | chr10 | 28620748 | |||||
| chr10:28620750
|
A | G | 1 | a0001c0001t0104 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1144A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1144 | chr10 | 28620750 | |||||
| chr10:28620921
|
A | G | 1 | a0001c0001t0103 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1315A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1315 | chr10 | 28620921 | |||||
| chr10:28620996
|
A | G | 1 | a0001c0001t0102 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1390A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1390 | chr10 | 28620996 | |||||
| chr10:28620997
|
T | A | 1 | a0001c0001t0105 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1391T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1391 | chr10 | 28620997 | |||||
| chr10:28621090
|
A | G | 14 | a0001c0001t0003a0001c0001t0010a0001c0001t0024others(11): Show | 33 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1484A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1484 | chr10 | 28621090 | |||||
| chr10:28621127
|
T | A | 1 | a0001c0001t0102 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1521T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1521 | chr10 | 28621127 | |||||
| chr10:28621154
|
A | C | 1 | a0001c0001t0102 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1548A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1548 | chr10 | 28621154 | |||||
| chr10:28621163
|
TTTC | T | 6 | a0001c0001t0097a0001c0001t0098a0001c0001t0120others(3): Show | 12 | HG00673.hp2 HG00735.hp2 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1572_*1574delCTT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1572 | INFO_REALIGN_3_PRIME | chr10 | 28621163 | ||||
| chr10:28621166
|
C | T | 140 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(137): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*1560C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1560 | chr10 | 28621166 | |||||
| chr10:28621169
|
C | T | 6 | a0001c0001t0097a0001c0001t0098a0001c0001t0120others(3): Show | 12 | HG00673.hp2 HG00735.hp2 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1563C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1563 | chr10 | 28621169 | |||||
| chr10:28621178
|
C | CT | 24 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(21): Show | 52 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1580dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1581 | INFO_REALIGN_3_PRIME | chr10 | 28621178 | ||||
| chr10:28621181
|
T | C | 1 | a0001c0001t0067 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1575T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1575 | chr10 | 28621181 | |||||
| chr10:28621186
|
TC | T | 5 | a0001c0001t0068a0001c0001t0070a0001c0001t0071others(2): Show | 5 | HG01069.hp1 HG01168.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1581delC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1581 | chr10 | 28621186 | |||||
| chr10:28621187
|
C | T | 135 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(132): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1581C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1581 | chr10 | 28621187 | |||||
| chr10:28621215
|
A | AT | 8 | a0001c0001t0026a0001c0001t0038a0001c0001t0040others(5): Show | 12 | HG00733.hp1 HG01123.hp2 HG02004.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1629dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1630 | INFO_REALIGN_3_PRIME | chr10 | 28621215 | ||||
| chr10:28621215
|
AT | A | 72 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(69): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*1629delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1629 | INFO_REALIGN_3_PRIME | chr10 | 28621215 | ||||
| chr10:28621215
|
ATT | A | 52 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(49): Show | 129 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1628_*1629delTT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1628 | INFO_REALIGN_3_PRIME | chr10 | 28621215 | ||||
| chr10:28621268
|
C | T | 2 | a0001c0001t0023a0001c0001t0056 | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1662C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1662 | chr10 | 28621268 | |||||
| chr10:28621270
|
G | A | 1 | a0001c0001t0066 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1664G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1664 | chr10 | 28621270 | |||||
| chr10:28621320
|
T | C | 1 | a0001c0001t0102 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1714T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1714 | chr10 | 28621320 | |||||
| chr10:28621379
|
T | A | 1 | a0001c0001t0134 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1773T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1773 | chr10 | 28621379 | |||||
| chr10:28621443
|
G | T | 31 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(28): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1837G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1837 | chr10 | 28621443 | |||||
| chr10:28621568
|
GT | G | 4 | a0001c0002t0013a0001c0002t0035a0001c0002t0072others(1): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1965delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1965 | INFO_REALIGN_3_PRIME | chr10 | 28621568 | ||||
| chr10:28621570
|
T | C | 4 | a0001c0002t0013a0001c0002t0035a0001c0002t0072others(1): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1964T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1964 | chr10 | 28621570 | |||||
| chr10:28621575
|
C | A | 4 | a0001c0002t0013a0001c0002t0035a0001c0002t0072others(1): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1969C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1969 | chr10 | 28621575 | |||||
| chr10:28621594
|
A | G | 1 | a0001c0001t0155 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1988A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 1988 | chr10 | 28621594 | |||||
| chr10:28621786
|
C | T | 98 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(95): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*2180C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2180 | chr10 | 28621786 | |||||
| chr10:28621789
|
T | A | 1 | a0001c0001t0066 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2183T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2183 | chr10 | 28621789 | |||||
| chr10:28621995
|
G | A | 139 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(136): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*2389G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2389 | chr10 | 28621995 | |||||
| chr10:28622050
|
T | C | 98 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(95): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*2444T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2444 | chr10 | 28622050 | |||||
| chr10:28622208
|
A | G | 1 | a0001c0001t0059 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2602A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2602 | chr10 | 28622208 | |||||
| chr10:28622374
|
T | C | 55 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(52): Show | 122 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*2768T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2768 | chr10 | 28622374 | |||||
| chr10:28622425
|
G | GC | 18 | a0001c0001t0010a0001c0001t0017a0001c0001t0027others(15): Show | 32 | HG00140.hp1 HG00621.hp2 HG01069.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2838dupC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | ||||
| chr10:28622425
|
G | GCC | 19 | a0001c0001t0001a0001c0001t0004a0001c0001t0016others(16): Show | 48 | HG00140.hp2 HG00558.hp1 HG00673.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2837_*2838dupCC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | ||||
| chr10:28622425
|
G | GCCC | 17 | a0001c0001t0005a0001c0001t0007a0001c0001t0019others(14): Show | 35 | HG00621.hp1 HG00673.hp1 HG00741.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2836_*2838dupCCC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | ||||
| chr10:28622425
|
G | GCCCC | 15 | a0001c0001t0030a0001c0001t0043a0001c0001t0047others(12): Show | 18 | HG00099.hp2 HG00609.hp1 HG01106.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2835_*2838dupCCCC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | ||||
| chr10:28622425
|
G | GCCCCC | 10 | a0001c0001t0014a0001c0001t0018a0001c0001t0024others(7): Show | 20 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2834_*2838dupCCCC others(1): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | ||||
| chr10:28622425
|
G | GCCCCCCC others(5): Show |
1 | a0001c0001t0135 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2827_*2838dupCCCC others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | ||||
| chr10:28622425
|
G | GGCCCCCC others(3): Show |
1 | a0001c0001t0139 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2819_*2820insGCCC others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2820 | chr10 | 28622425 | |||||
| chr10:28622425
|
GC | G | 18 | a0001c0001t0002a0001c0001t0011a0001c0001t0029others(15): Show | 43 | HG00438.hp2 HG00558.hp2 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2838delC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2838 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | ||||
| chr10:28622425
|
GCC | G | 14 | a0001c0001t0006a0001c0001t0022a0001c0001t0025others(11): Show | 30 | HG00609.hp2 HG00639.hp2 HG00642.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2837_*2838delCC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2837 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | ||||
| chr10:28622425
|
GCCC | G | 13 | a0001c0001t0031a0001c0001t0056a0001c0001t0066others(10): Show | 15 | HG00735.hp2 HG01123.hp2 HG01891.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2836_*2838delCCC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2836 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | ||||
| chr10:28622425
|
GCCCCCCC others(4): Show |
G | 3 | a0001c0004t0069a0001c0004t0078a0001c0004t0079 | 3 | HG01069.hp1 HG02055.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2828_*2838delCCCC others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2828 | INFO_REALIGN_3_PRIME | chr10 | 28622425 | ||||
| chr10:28622437
|
C | T | 1 | a0001c0001t0154 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2831C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2831 | chr10 | 28622437 | |||||
| chr10:28622442
|
C | G | 1 | a0001c0001t0104 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2836C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2836 | chr10 | 28622442 | |||||
| chr10:28622444
|
C | G | 2 | a0001c0001t0066a0001c0004t0079 | 2 | HG06807.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2838C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2838 | chr10 | 28622444 | |||||
| chr10:28622445
|
G | T | 1 | a0001c0001t0066 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2839G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2839 | chr10 | 28622445 | |||||
| chr10:28622462
|
GTC | G | 3 | a0001c0001t0074a0001c0001t0076a0001c0001t0077 | 3 | HG02717.hp2 HG03130.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2860_*2861delCT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2860 | INFO_REALIGN_3_PRIME | chr10 | 28622462 | ||||
| chr10:28622539
|
G | T | 1 | a0001c0001t0075 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2933G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2933 | chr10 | 28622539 | |||||
| chr10:28622564
|
T | A | 1 | a0001c0001t0066 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2958T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2958 | chr10 | 28622564 | |||||
| chr10:28622566
|
T | C | 1 | a0001c0001t0150 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2960T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 2960 | chr10 | 28622566 | |||||
| chr10:28622693
|
T | C | 1 | a0001c0001t0136 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3087T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 3087 | chr10 | 28622693 | |||||
| chr10:28622793
|
A | G | 1 | a0001c0001t0123 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3187A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 3187 | chr10 | 28622793 | |||||
| chr10:28622909
|
A | G | 1 | a0001c0001t0073 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3303A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 3303 | chr10 | 28622909 | |||||
| chr10:28622968
|
A | G | 2 | a0001c0001t0137a0001c0001t0138 | 2 | NA18978.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3362A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 14/14 | 3362 | chr10 | 28622968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:28533630
|
C | T | 1 | a0001c0001t0100g0320 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.41+10C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | chr10 | 28533630 | ||||||
| chr10:28533659
|
G | GGGCGGC | 8 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(5): Show | 8 | HG00735.hp2 HG02055.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.41+45_41+50dupCGGC others(2): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 28533659 | |||||
| chr10:28533777
|
G | T | 1 | a0001c0001t0009g0319 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.41+157G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | chr10 | 28533777 | ||||||
| chr10:28533812
|
C | T | 1 | a0001c0001t0011g0318 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.42-186C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | chr10 | 28533812 | ||||||
| chr10:28533840
|
C | T | 1 | a0001c0001t0143g0317 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.42-158C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | chr10 | 28533840 | ||||||
| chr10:28533924
|
G | A | 1 | a0001c0001t0011g0318 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.42-74G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | chr10 | 28533924 | ||||||
| chr10:28533978
|
C | T | 4 | a0001c0001t0004g0314a0001c0001t0007g0313a0001c0001t0046g0315others(1): Show | 4 | NA18967.hp1 NA18998.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-20C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 1/13 | chr10 | 28533978 | ||||||
| chr10:28534053
|
G | T | 3 | a0001c0001t0029g0311a0001c0001t0029g0312a0001c0001t0058g0310 | 3 | HG00639.hp1 HG01175.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.78+19G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534053 | ||||||
| chr10:28534057
|
A | G | 2 | a0001c0001t0033g0309a0001c0001t0119g0308 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.78+23A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534057 | ||||||
| chr10:28534197
|
G | A | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.78+163G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534197 | ||||||
| chr10:28534340
|
A | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.78+306A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534340 | ||||||
| chr10:28534343
|
A | T | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.78+309A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534343 | ||||||
| chr10:28534409
|
G | T | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.78+375G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534409 | ||||||
| chr10:28534452
|
T | G | 1 | a0001c0001t0052g0066 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.78+418T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534452 | ||||||
| chr10:28534520
|
C | T | 7 | a0001c0001t0028g0285a0001c0001t0028g0290a0001c0001t0043g0289others(4): Show | 7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+486C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534520 | ||||||
| chr10:28534641
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.78+607A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534641 | ||||||
| chr10:28534787
|
T | A | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.78+753T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534787 | ||||||
| chr10:28534835
|
A | T | 1 | a0001c0001t0006g0284 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.79-727A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534835 | ||||||
| chr10:28534920
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.79-642A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534920 | ||||||
| chr10:28534955
|
G | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.79-607G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28534955 | ||||||
| chr10:28535046
|
A | T | 1 | a0001c0001t0018g0283 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.79-516A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535046 | ||||||
| chr10:28535118
|
GT | G | 188 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(185): Show | 188 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.79-427delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 28535118 | |||||
| chr10:28535154
|
T | C | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.79-408T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535154 | ||||||
| chr10:28535161
|
GCTTA | G | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.79-400_79-397delCT others(2): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535161 | ||||||
| chr10:28535332
|
TG | T | 5 | a0001c0001t0006g0069a0001c0001t0023g0070a0001c0001t0023g0254others(2): Show | 5 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-227delG | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 28535332 | |||||
| chr10:28535334
|
G | GT | 3 | a0001c0001t0002g0219a0001c0001t0005g0282a0001c0001t0030g0218 | 3 | HG01123.hp1 HG02559.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.79-228_79-227insT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535334 | ||||||
| chr10:28535335
|
G | T | 219 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.79-227G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535335 | ||||||
| chr10:28535353
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.79-209G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535353 | ||||||
| chr10:28535461
|
T | C | 1 | a0001c0001t0131g0013 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.79-101T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535461 | ||||||
| chr10:28535484
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.79-78A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 2/13 | chr10 | 28535484 | ||||||
| chr10:28535887
|
A | AT | 26 | a0001c0001t0004g0054a0001c0001t0004g0058a0001c0001t0004g0314others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.274+140dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28535887 | |||||
| chr10:28536013
|
G | A | 7 | a0001c0001t0028g0285a0001c0001t0028g0290a0001c0001t0043g0289others(4): Show | 7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+256G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536013 | ||||||
| chr10:28536086
|
C | G | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.274+329C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536086 | ||||||
| chr10:28536243
|
A | G | 1 | a0001c0001t0105g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274+486A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536243 | ||||||
| chr10:28536245
|
TA | T | 282 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(279): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.274+503delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28536245 | |||||
| chr10:28536279
|
T | A | 1 | a0001c0001t0014g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.274+522T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536279 | ||||||
| chr10:28536313
|
A | G | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+556A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536313 | ||||||
| chr10:28536382
|
TTTCAGTT others(18): Show |
T | 1 | a0001c0001t0105g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274+635_274+659del others(25): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28536382 | |||||
| chr10:28536760
|
C | T | 122 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(119): Show | 122 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.274+1003C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536760 | ||||||
| chr10:28536956
|
G | A | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.274+1199G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28536956 | ||||||
| chr10:28537340
|
C | T | 1 | a0001c0001t0059g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.274+1583C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537340 | ||||||
| chr10:28537462
|
C | G | 6 | a0001c0001t0012g0277a0001c0001t0018g0278a0001c0001t0018g0283others(3): Show | 6 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+1705C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537462 | ||||||
| chr10:28537499
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+1742A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537499 | ||||||
| chr10:28537630
|
C | T | 1 | a0001c0001t0032g0216 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.274+1873C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537630 | ||||||
| chr10:28537654
|
A | T | 2 | a0001c0001t0014g0215a0001c0001t0017g0214 | 2 | HG00735.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.274+1897A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537654 | ||||||
| chr10:28537901
|
G | C | 1 | a0001c0001t0053g0107 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.274+2144G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537901 | ||||||
| chr10:28537901
|
G | T | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.274+2144G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537901 | ||||||
| chr10:28537919
|
G | A | 1 | a0001c0001t0018g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.274+2162G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537919 | ||||||
| chr10:28537958
|
C | T | 1 | a0001c0001t0005g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.274+2201C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28537958 | ||||||
| chr10:28538022
|
C | G | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+2265C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538022 | ||||||
| chr10:28538063
|
T | G | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.274+2306T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538063 | ||||||
| chr10:28538076
|
C | T | 1 | a0001c0001t0009g0211 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.274+2319C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538076 | ||||||
| chr10:28538167
|
A | T | 1 | a0001c0001t0006g0069 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.274+2410A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538167 | ||||||
| chr10:28538323
|
C | T | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+2566C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538323 | ||||||
| chr10:28538324
|
G | A | 1 | a0001c0001t0102g0280 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.274+2567G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538324 | ||||||
| chr10:28538407
|
C | G | 7 | a0001c0001t0028g0285a0001c0001t0028g0290a0001c0001t0043g0289others(4): Show | 7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+2650C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538407 | ||||||
| chr10:28538538
|
T | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+2781T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538538 | ||||||
| chr10:28538581
|
C | CA | 57 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(54): Show | 57 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.274+2844dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28538581 | |||||
| chr10:28538581
|
CA | C | 210 | a0001c0001t0001g0067a0001c0001t0001g0126a0001c0001t0001g0130others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.274+2844delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28538581 | |||||
| chr10:28538663
|
G | A | 1 | a0001c0001t0007g0313 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.274+2906G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538663 | ||||||
| chr10:28538695
|
G | T | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+2938G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538695 | ||||||
| chr10:28538810
|
G | A | 2 | a0001c0001t0008g0048a0001c0001t0146g0047 | 2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.274+3053G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538810 | ||||||
| chr10:28538866
|
T | TA | 18 | a0001c0001t0004g0014a0001c0001t0021g0002a0001c0001t0021g0292others(15): Show | 18 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.274+3127dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28538866 | |||||
| chr10:28538866
|
TA | T | 199 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.274+3127delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28538866 | |||||
| chr10:28538866
|
TAA | T | 7 | a0001c0001t0002g0210a0001c0001t0005g0208a0001c0001t0033g0309others(4): Show | 7 | HG01167.hp1 HG01943.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+3126_274+3127d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28538866 | |||||
| chr10:28538914
|
C | T | 64 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.274+3157C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538914 | ||||||
| chr10:28538958
|
C | T | 1 | a0001c0001t0005g0282 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.274+3201C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28538958 | ||||||
| chr10:28539014
|
A | G | 1 | a0001c0001t0007g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274+3257A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539014 | ||||||
| chr10:28539055
|
G | T | 59 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.274+3298G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539055 | ||||||
| chr10:28539145
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+3388C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539145 | ||||||
| chr10:28539173
|
A | G | 1 | a0001c0001t0105g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274+3416A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539173 | ||||||
| chr10:28539216
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+3459C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539216 | ||||||
| chr10:28539308
|
C | T | 1 | a0001c0001t0054g0207 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.274+3551C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539308 | ||||||
| chr10:28539352
|
G | C | 1 | a0001c0001t0003g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.274+3595G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539352 | ||||||
| chr10:28539398
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.274+3641G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539398 | ||||||
| chr10:28539425
|
A | G | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+3668A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539425 | ||||||
| chr10:28539553
|
C | T | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+3796C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539553 | ||||||
| chr10:28539554
|
G | A | 1 | a0001c0001t0005g0118 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.274+3797G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539554 | ||||||
| chr10:28539571
|
G | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+3814G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539571 | ||||||
| chr10:28539572
|
GT | G | 286 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.274+3826delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28539572 | |||||
| chr10:28539597
|
T | C | 297 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.274+3840T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539597 | ||||||
| chr10:28539838
|
C | T | 63 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.274+4081C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28539838 | ||||||
| chr10:28540003
|
T | A | 1 | a0001c0001t0047g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.274+4246T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28540003 | ||||||
| chr10:28540178
|
T | G | 1 | a0001c0001t0006g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.274+4421T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28540178 | ||||||
| chr10:28540330
|
A | T | 2 | a0001c0001t0070g0275a0001c0001t0088g0279 | 2 | HG01168.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.274+4573A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28540330 | ||||||
| chr10:28540602
|
A | C | 1 | a0001c0001t0012g0274 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.274+4845A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28540602 | ||||||
| chr10:28540608
|
G | A | 1 | a0001c0001t0017g0120 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.274+4851G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28540608 | ||||||
| chr10:28540669
|
G | A | 1 | a0001c0001t0018g0283 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.274+4912G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28540669 | ||||||
| chr10:28540870
|
CTTCA | C | 4 | a0001c0001t0021g0002a0001c0001t0021g0304a0001c0001t0022g0002others(1): Show | 4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+5116_274+5119d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28540870 | |||||
| chr10:28541106
|
A | C | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+5349A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541106 | ||||||
| chr10:28541179
|
T | C | 68 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.274+5422T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541179 | ||||||
| chr10:28541368
|
A | G | 2 | a0001c0001t0070g0275a0001c0001t0088g0279 | 2 | HG01168.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.274+5611A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541368 | ||||||
| chr10:28541404
|
T | G | 121 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(118): Show | 121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.274+5647T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541404 | ||||||
| chr10:28541415
|
G | GT | 6 | a0001c0001t0008g0017a0001c0001t0022g0302a0001c0001t0022g0303others(3): Show | 6 | HG00609.hp2 HG01069.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+5662dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | |||||
| chr10:28541415
|
G | GTT | 26 | a0001c0001t0004g0026a0001c0001t0004g0045a0001c0001t0004g0054others(23): Show | 26 | HG00323.hp2 HG00673.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.274+5661_274+5662d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | |||||
| chr10:28541415
|
G | GTTT | 15 | a0001c0001t0004g0014a0001c0001t0004g0029a0001c0001t0004g0031others(12): Show | 15 | HG01167.hp2 HG01358.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.274+5660_274+5662d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | |||||
| chr10:28541415
|
G | GTTTT | 5 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0007g0062others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.274+5659_274+5662d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | |||||
| chr10:28541415
|
G | GTTTTT | 7 | a0001c0001t0008g0011a0001c0001t0008g0037a0001c0001t0048g0063others(4): Show | 7 | HG01109.hp2 HG01175.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.274+5662_274+5663i others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | |||||
| chr10:28541415
|
GTTT | G | 4 | a0001c0001t0010g0080a0001c0001t0012g0221a0001c0001t0012g0222others(1): Show | 4 | HG01891.hp2 NA18971.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+5660_274+5662d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | |||||
| chr10:28541415
|
GTTTTGTT others(2): Show |
G | 7 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0006g0122others(4): Show | 7 | HG02055.hp1 NA18969.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+5663_274+5671d others(11): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | |||||
| chr10:28541415
|
GTTTTGTT others(10): Show |
G | 1 | a0001c0001t0145g0050 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.274+5663_274+5679d others(19): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541415 | |||||
| chr10:28541416
|
T | TG | 12 | a0001c0001t0002g0202a0001c0001t0002g0204a0001c0001t0006g0119others(9): Show | 12 | HG00642.hp1 HG01934.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.274+5659_274+5660i others(3): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541416 | ||||||
| chr10:28541417
|
T | G | 166 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0130others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.274+5660T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541417 | ||||||
| chr10:28541417
|
TTTG | T | 6 | a0001c0001t0056g0255a0001c0002t0013g0003a0001c0002t0013g0005others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+5663_274+5665d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541417 | |||||
| chr10:28541418
|
T | G | 5 | a0001c0001t0009g0121a0001c0001t0012g0274a0001c0001t0018g0257others(2): Show | 5 | HG00738.hp1 HG01934.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+5661T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541418 | ||||||
| chr10:28541418
|
TTG | T | 29 | a0001c0001t0001g0130a0001c0001t0002g0132a0001c0001t0003g0076others(26): Show | 29 | HG00140.hp1 HG00673.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.274+5663_274+5664d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541418 | |||||
| chr10:28541419
|
T | G | 3 | a0001c0001t0062g0078a0001c0001t0063g0105a0001c0001t0064g0077 | 3 | HG01496.hp1 HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.274+5662T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541419 | ||||||
| chr10:28541419
|
TG | T | 103 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0140others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.274+5663delG | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541419 | ||||||
| chr10:28541420
|
G | GT | 8 | a0001c0001t0011g0249a0001c0001t0025g0224a0001c0001t0026g0231others(5): Show | 8 | HG00438.hp2 HG00621.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.274+5689dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28541420 | |||||
| chr10:28541420
|
G | T | 130 | a0001c0001t0001g0186a0001c0001t0001g0193a0001c0001t0001g0197others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.274+5663G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541420 | ||||||
| chr10:28541426
|
T | G | 7 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0006g0122others(4): Show | 7 | HG02055.hp1 NA18969.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+5669T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541426 | ||||||
| chr10:28541432
|
T | G | 1 | a0001c0001t0105g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274+5675T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541432 | ||||||
| chr10:28541436
|
T | G | 1 | a0001c0001t0105g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274+5679T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541436 | ||||||
| chr10:28541461
|
C | G | 1 | a0001c0001t0120g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.274+5704C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541461 | ||||||
| chr10:28541501
|
A | G | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.274+5744A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541501 | ||||||
| chr10:28541609
|
T | C | 1 | a0001c0001t0002g0138 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.274+5852T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541609 | ||||||
| chr10:28541615
|
A | G | 1 | a0001c0001t0012g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.274+5858A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541615 | ||||||
| chr10:28541861
|
G | T | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+6104G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541861 | ||||||
| chr10:28541928
|
C | G | 2 | a0001c0001t0003g0085a0001c0001t0010g0096 | 2 | NA18959.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.274+6171C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541928 | ||||||
| chr10:28541969
|
C | T | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+6212C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28541969 | ||||||
| chr10:28542071
|
T | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+6314T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542071 | ||||||
| chr10:28542112
|
T | A | 3 | a0001c0001t0003g0097a0001c0001t0010g0098a0001c0001t0010g0272 | 3 | HG00597.hp2 HG02056.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.274+6355T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542112 | ||||||
| chr10:28542137
|
A | G | 1 | a0001c0001t0091g0179 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.274+6380A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542137 | ||||||
| chr10:28542173
|
C | T | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.274+6416C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542173 | ||||||
| chr10:28542251
|
A | T | 1 | a0001c0001t0100g0320 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.274+6494A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542251 | ||||||
| chr10:28542317
|
T | G | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.274+6560T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542317 | ||||||
| chr10:28542536
|
C | T | 1 | a0001c0001t0093g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.274+6779C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542536 | ||||||
| chr10:28542635
|
T | C | 3 | a0001c0001t0034g0260a0001c0001t0067g0269a0001c0001t0127g0261 | 3 | HG01256.hp2 HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.274+6878T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542635 | ||||||
| chr10:28542640
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+6883C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28542640 | ||||||
| chr10:28543161
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+7404C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543161 | ||||||
| chr10:28543182
|
G | C | 4 | a0001c0001t0002g0180a0001c0001t0002g0202a0001c0001t0006g0116others(1): Show | 4 | HG01358.hp2 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+7425G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543182 | ||||||
| chr10:28543264
|
A | G | 1 | a0001c0001t0084g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.274+7507A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543264 | ||||||
| chr10:28543322
|
AT | A | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.274+7569delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28543322 | |||||
| chr10:28543404
|
T | G | 1 | a0001c0001t0015g0181 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.274+7647T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543404 | ||||||
| chr10:28543437
|
A | G | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+7680A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543437 | ||||||
| chr10:28543632
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+7875A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543632 | ||||||
| chr10:28543648
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+7891A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543648 | ||||||
| chr10:28543709
|
C | T | 4 | a0001c0001t0001g0175a0001c0001t0002g0174a0001c0001t0002g0210others(1): Show | 4 | HG02155.hp2 NA18967.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+7952C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543709 | ||||||
| chr10:28543783
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+8026A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543783 | ||||||
| chr10:28543813
|
C | T | 8 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0219others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+8056C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543813 | ||||||
| chr10:28543872
|
G | GT | 32 | a0001c0001t0012g0265a0001c0001t0012g0274a0001c0001t0012g0277others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.274+8121dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28543872 | |||||
| chr10:28543891
|
G | C | 67 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.274+8134G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543891 | ||||||
| chr10:28543965
|
C | T | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+8208C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543965 | ||||||
| chr10:28543969
|
A | G | 1 | a0001c0001t0005g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.274+8212A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28543969 | ||||||
| chr10:28544013
|
G | T | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+8256G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544013 | ||||||
| chr10:28544089
|
G | T | 4 | a0002c0003t0026g0068a0002c0003t0026g0229a0002c0003t0041g0223others(1): Show | 4 | HG01123.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.274+8332G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544089 | ||||||
| chr10:28544187
|
C | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+8430C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544187 | ||||||
| chr10:28544229
|
T | C | 34 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(31): Show | 34 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.274+8472T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544229 | ||||||
| chr10:28544248
|
C | T | 7 | a0001c0001t0028g0285a0001c0001t0028g0290a0001c0001t0043g0289others(4): Show | 7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+8491C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544248 | ||||||
| chr10:28544254
|
G | T | 8 | a0001c0001t0002g0168a0001c0001t0002g0204a0001c0001t0006g0119others(5): Show | 8 | HG00642.hp1 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+8497G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544254 | ||||||
| chr10:28544471
|
C | T | 1 | a0001c0001t0105g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274+8714C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544471 | ||||||
| chr10:28544965
|
C | T | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+9208C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28544965 | ||||||
| chr10:28545040
|
CA | C | 94 | a0001c0001t0002g0138a0001c0001t0004g0014a0001c0001t0004g0026others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.274+9303delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28545040 | |||||
| chr10:28545040
|
CAA | C | 32 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(29): Show | 32 | HG00735.hp2 HG01099.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.274+9302_274+9303d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28545040 | |||||
| chr10:28545040
|
CAAA | C | 118 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(115): Show | 118 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.274+9301_274+9303d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28545040 | |||||
| chr10:28545049
|
A | C | 1 | a0001c0001t0092g0199 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.274+9292A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545049 | ||||||
| chr10:28545266
|
C | T | 2 | a0001c0001t0037g0247a0001c0001t0125g0246 | 2 | NA18612.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.274+9509C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545266 | ||||||
| chr10:28545324
|
C | T | 1 | a0001c0001t0135g0034 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.274+9567C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545324 | ||||||
| chr10:28545580
|
C | T | 1 | a0001c0001t0145g0050 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.274+9823C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545580 | ||||||
| chr10:28545611
|
T | A | 1 | a0001c0001t0008g0011 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.274+9854T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545611 | ||||||
| chr10:28545759
|
A | G | 4 | a0001c0001t0001g0175a0001c0001t0002g0174a0001c0001t0002g0210others(1): Show | 4 | HG02155.hp2 NA18967.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+10002A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545759 | ||||||
| chr10:28545874
|
C | T | 1 | a0001c0001t0006g0116 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.274+10117C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545874 | ||||||
| chr10:28545999
|
C | G | 4 | a0001c0001t0021g0002a0001c0001t0021g0304a0001c0001t0022g0002others(1): Show | 4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+10242C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28545999 | ||||||
| chr10:28546172
|
G | A | 1 | a0001c0001t0022g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.274+10415G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28546172 | ||||||
| chr10:28546344
|
G | A | 2 | a0001c0001t0033g0309a0001c0001t0119g0308 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.274+10587G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28546344 | ||||||
| chr10:28546534
|
G | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.274+10777G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28546534 | ||||||
| chr10:28546670
|
TTAAA | T | 3 | a0001c0001t0074g0164a0001c0001t0076g0166a0001c0001t0077g0165 | 3 | HG02717.hp2 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.274+10919_274+1092 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28546670 | |||||
| chr10:28546721
|
C | T | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+10964C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28546721 | ||||||
| chr10:28546867
|
CT | C | 82 | a0001c0001t0002g0174a0001c0001t0003g0076a0001c0001t0003g0083others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.274+11122delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28546867 | |||||
| chr10:28547158
|
G | T | 203 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.274+11401G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547158 | ||||||
| chr10:28547185
|
T | C | 1 | a0001c0001t0002g0204 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.274+11428T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547185 | ||||||
| chr10:28547245
|
G | A | 21 | a0001c0001t0012g0222a0001c0001t0021g0002a0001c0001t0021g0292others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.274+11488G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547245 | ||||||
| chr10:28547302
|
A | G | 83 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(80): Show | 83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.274+11545A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547302 | ||||||
| chr10:28547326
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+11569G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547326 | ||||||
| chr10:28547364
|
G | A | 6 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0140others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+11607G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547364 | ||||||
| chr10:28547436
|
G | A | 1 | a0001c0001t0008g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.274+11679G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547436 | ||||||
| chr10:28547541
|
A | T | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+11784A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547541 | ||||||
| chr10:28547770
|
C | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+12013C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547770 | ||||||
| chr10:28547780
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+12023A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547780 | ||||||
| chr10:28547833
|
T | C | 1 | a0001c0001t0007g0030 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.274+12076T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547833 | ||||||
| chr10:28547847
|
C | CT | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+12096dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28547847 | |||||
| chr10:28547854
|
C | G | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+12097C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547854 | ||||||
| chr10:28547869
|
G | A | 1 | a0001c0001t0006g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.274+12112G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547869 | ||||||
| chr10:28547915
|
C | CT | 182 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.274+12173dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28547915 | |||||
| chr10:28547915
|
CT | C | 11 | a0001c0001t0154g0307a0001c0002t0013g0003a0001c0002t0013g0005others(8): Show | 11 | HG00735.hp2 HG02055.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.274+12173delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28547915 | |||||
| chr10:28547918
|
T | TC | 7 | a0001c0001t0016g0141a0001c0001t0016g0142a0001c0001t0016g0143others(4): Show | 7 | HG02083.hp1 HG02129.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+12161_274+1216 others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547918 | ||||||
| chr10:28547950
|
C | T | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+12193C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547950 | ||||||
| chr10:28547951
|
G | A | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.274+12194G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547951 | ||||||
| chr10:28547962
|
T | C | 9 | a0001c0001t0002g0168a0001c0001t0002g0204a0001c0001t0006g0119others(6): Show | 9 | HG00642.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.274+12205T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28547962 | ||||||
| chr10:28548014
|
G | A | 1 | a0001c0001t0014g0203 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.274+12257G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548014 | ||||||
| chr10:28548216
|
G | A | 1 | a0001c0001t0047g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.274+12459G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548216 | ||||||
| chr10:28548248
|
T | C | 1 | a0001c0001t0092g0199 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.274+12491T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548248 | ||||||
| chr10:28548294
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+12537G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548294 | ||||||
| chr10:28548457
|
C | G | 1 | a0001c0001t0014g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.274+12700C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548457 | ||||||
| chr10:28548567
|
C | T | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+12810C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548567 | ||||||
| chr10:28548682
|
G | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.274+12925G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548682 | ||||||
| chr10:28548797
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.274+13040A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28548797 | ||||||
| chr10:28549038
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+13281G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549038 | ||||||
| chr10:28549058
|
C | G | 193 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.274+13301C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549058 | ||||||
| chr10:28549158
|
CAA | C | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.274+13403_274+1340 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28549158 | |||||
| chr10:28549201
|
G | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+13444G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549201 | ||||||
| chr10:28549273
|
A | G | 1 | a0001c0001t0015g0198 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.274+13516A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549273 | ||||||
| chr10:28549389
|
A | G | 1 | a0001c0001t0107g0232 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.274+13632A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549389 | ||||||
| chr10:28549404
|
T | C | 1 | a0001c0001t0032g0145 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.274+13647T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549404 | ||||||
| chr10:28549506
|
C | G | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+13749C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549506 | ||||||
| chr10:28549520
|
T | C | 4 | a0001c0001t0024g0079a0001c0001t0062g0078a0001c0001t0063g0105others(1): Show | 4 | HG01496.hp1 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+13763T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549520 | ||||||
| chr10:28549643
|
T | C | 297 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.274+13886T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549643 | ||||||
| chr10:28549763
|
T | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+14006T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549763 | ||||||
| chr10:28549890
|
C | T | 1 | a0001c0001t0028g0290 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.274+14133C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549890 | ||||||
| chr10:28549891
|
G | A | 1 | a0001c0001t0037g0251 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.274+14134G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549891 | ||||||
| chr10:28549938
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+14181A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28549938 | ||||||
| chr10:28550110
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+14353G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550110 | ||||||
| chr10:28550123
|
C | G | 7 | a0001c0001t0028g0285a0001c0001t0028g0290a0001c0001t0043g0289others(4): Show | 7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+14366C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550123 | ||||||
| chr10:28550166
|
C | CA | 225 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(222): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.274+14423dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28550166 | |||||
| chr10:28550291
|
C | CT | 20 | a0001c0001t0012g0221a0001c0001t0012g0265a0001c0001t0012g0274others(17): Show | 20 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.274+14546dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28550291 | |||||
| chr10:28550343
|
T | C | 1 | a0001c0001t0007g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274+14586T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550343 | ||||||
| chr10:28550550
|
G | A | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+14793G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550550 | ||||||
| chr10:28550597
|
T | C | 22 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0085others(19): Show | 22 | HG00597.hp1 HG00597.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.274+14840T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550597 | ||||||
| chr10:28550768
|
T | C | 7 | a0001c0001t0028g0285a0001c0001t0028g0290a0001c0001t0043g0289others(4): Show | 7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+15011T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550768 | ||||||
| chr10:28550901
|
G | A | 2 | a0001c0001t0025g0224a0001c0001t0025g0233 | 2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.274+15144G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28550901 | ||||||
| chr10:28551124
|
T | G | 203 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.274+15367T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551124 | ||||||
| chr10:28551185
|
A | C | 193 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.274+15428A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551185 | ||||||
| chr10:28551195
|
C | T | 18 | a0001c0001t0012g0265a0001c0001t0012g0274a0001c0001t0018g0257others(15): Show | 18 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.274+15438C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551195 | ||||||
| chr10:28551459
|
G | T | 3 | a0001c0001t0034g0260a0001c0001t0067g0269a0001c0001t0127g0261 | 3 | HG01256.hp2 HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.274+15702G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551459 | ||||||
| chr10:28551586
|
A | G | 1 | a0001c0001t0120g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.274+15829A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551586 | ||||||
| chr10:28551784
|
T | TTG | 8 | a0001c0001t0002g0168a0001c0001t0011g0249a0001c0001t0012g0222others(5): Show | 8 | HG00733.hp1 HG01361.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+16061_274+1606 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | |||||
| chr10:28551784
|
T | TTGTG | 33 | a0001c0001t0001g0160a0001c0001t0001g0175a0001c0001t0002g0161others(30): Show | 33 | HG00140.hp1 HG00642.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.274+16059_274+1606 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | |||||
| chr10:28551784
|
T | TTGTGTG | 28 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0101others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.274+16057_274+1606 others(10): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | |||||
| chr10:28551784
|
T | TTGTGTGT others(1): Show |
39 | a0001c0001t0001g0126a0001c0001t0001g0158a0001c0001t0001g0170others(36): Show | 39 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.274+16055_274+1606 others(12): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | |||||
| chr10:28551784
|
T | TTGTGTGT others(3): Show |
49 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0130others(46): Show | 49 | HG00140.hp2 HG00558.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.274+16053_274+1606 others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | |||||
| chr10:28551784
|
T | TTGTGTGT others(5): Show |
19 | a0001c0001t0001g0186a0001c0001t0005g0169a0001c0001t0005g0282others(16): Show | 19 | HG00438.hp1 HG01099.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.274+16051_274+1606 others(16): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | |||||
| chr10:28551784
|
T | TTGTGTGT others(7): Show |
12 | a0001c0001t0014g0072a0001c0001t0028g0285a0001c0001t0029g0311others(9): Show | 12 | HG00609.hp1 HG00639.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.274+16049_274+1606 others(18): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | |||||
| chr10:28551784
|
T | TTGTGTGT others(9): Show |
2 | a0001c0001t0001g0146a0001c0001t0092g0199 | 2 | NA18940.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.274+16047_274+1606 others(20): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | |||||
| chr10:28551784
|
TTGTGTG | T | 54 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(51): Show | 54 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.274+16057_274+1606 others(10): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | |||||
| chr10:28551784
|
TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0007g0030a0001c0001t0050g0018a0001c0001t0061g0268 | 3 | HG00609.hp2 HG03098.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.274+16055_274+1606 others(12): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | |||||
| chr10:28551784
|
TTGTGTGT others(9): Show |
T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+16047_274+1606 others(20): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551784 | |||||
| chr10:28551813
|
TGTGTG | T | 4 | a0001c0001t0007g0040a0001c0001t0007g0062a0001c0001t0007g0313others(1): Show | 4 | HG00621.hp1 HG04115.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.274+16057_274+1606 others(9): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551813 | ||||||
| chr10:28551816
|
G | T | 14 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(11): Show | 14 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.274+16059G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551816 | ||||||
| chr10:28551818
|
G | C | 14 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(11): Show | 14 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.274+16061G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551818 | ||||||
| chr10:28551818
|
G | T | 5 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+16061G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551818 | ||||||
| chr10:28551819
|
T | TC | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+16062_274+1606 others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551819 | ||||||
| chr10:28551819
|
T | TGTGTGTG others(4): Show |
3 | a0001c0001t0002g0132a0001c0001t0033g0258a0001c0001t0149g0291 | 3 | HG03704.hp1 HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.274+16062_274+1606 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551819 | ||||||
| chr10:28551819
|
T | TGTGTGTG others(6): Show |
2 | a0001c0001t0024g0086a0001c0001t0104g0306 | 2 | HG03041.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.274+16062_274+1606 others(17): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551819 | ||||||
| chr10:28551820
|
T | C | 1 | a0001c0001t0110g0295 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.274+16063T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551820 | ||||||
| chr10:28551820
|
TTC | T | 14 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(11): Show | 14 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.274+16065_274+1606 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28551820 | |||||
| chr10:28551821
|
T | C | 5 | a0001c0001t0007g0040a0001c0001t0007g0062a0001c0001t0007g0313others(2): Show | 5 | HG00621.hp1 HG02965.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+16064T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551821 | ||||||
| chr10:28551822
|
C | T | 16 | a0001c0001t0001g0197a0001c0001t0002g0132a0001c0001t0007g0040others(13): Show | 16 | HG00621.hp1 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+16065C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551822 | ||||||
| chr10:28551823
|
T | C | 6 | a0001c0001t0001g0197a0001c0001t0002g0132a0001c0001t0071g0108others(3): Show | 6 | HG03041.hp1 HG03704.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+16066T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551823 | ||||||
| chr10:28551974
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+16217G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28551974 | ||||||
| chr10:28552285
|
G | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.274+16528G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552285 | ||||||
| chr10:28552364
|
G | C | 1 | a0001c0001t0074g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.274+16607G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552364 | ||||||
| chr10:28552550
|
T | C | 1 | a0001c0001t0018g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.274+16793T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552550 | ||||||
| chr10:28552560
|
A | G | 1 | a0001c0001t0018g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.274+16803A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552560 | ||||||
| chr10:28552629
|
T | C | 1 | a0001c0001t0044g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.274+16872T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552629 | ||||||
| chr10:28552730
|
C | T | 1 | a0001c0001t0038g0245 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.274+16973C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552730 | ||||||
| chr10:28552822
|
CAGTG | C | 114 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(111): Show | 114 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.274+17068_274+1707 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28552822 | |||||
| chr10:28552823
|
A | G | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+17066A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552823 | ||||||
| chr10:28552840
|
G | A | 24 | a0001c0001t0012g0265a0001c0001t0012g0274a0001c0001t0012g0277others(21): Show | 24 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.274+17083G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552840 | ||||||
| chr10:28552845
|
C | CT | 27 | a0001c0001t0003g0084a0001c0001t0011g0243a0001c0001t0011g0249others(24): Show | 27 | HG00609.hp1 HG00621.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.274+17111dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28552845 | |||||
| chr10:28552845
|
CT | C | 42 | a0001c0001t0001g0158a0001c0001t0001g0197a0001c0001t0002g0138others(39): Show | 42 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.274+17111delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28552845 | |||||
| chr10:28552845
|
CTT | C | 152 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.274+17110_274+1711 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28552845 | |||||
| chr10:28552845
|
CTTT | C | 11 | a0001c0001t0002g0204a0001c0001t0006g0119a0001c0001t0008g0022others(8): Show | 11 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.274+17109_274+1711 others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28552845 | |||||
| chr10:28552845
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0013g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.274+17101_274+1711 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28552845 | |||||
| chr10:28552872
|
T | G | 1 | a0001c0001t0009g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.274+17115T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552872 | ||||||
| chr10:28552969
|
A | G | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+17212A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28552969 | ||||||
| chr10:28553103
|
A | G | 124 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(121): Show | 124 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.274+17346A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553103 | ||||||
| chr10:28553263
|
A | ATAAT | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.274+17507_274+1750 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28553263 | |||||
| chr10:28553338
|
T | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+17581T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553338 | ||||||
| chr10:28553348
|
C | G | 204 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.274+17591C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553348 | ||||||
| chr10:28553545
|
C | T | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.274+17788C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553545 | ||||||
| chr10:28553706
|
A | G | 1 | a0001c0002t0035g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.274+17949A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553706 | ||||||
| chr10:28553762
|
A | G | 1 | a0001c0001t0037g0251 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.274+18005A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553762 | ||||||
| chr10:28553765
|
G | A | 1 | a0001c0001t0012g0191 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.274+18008G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553765 | ||||||
| chr10:28553789
|
T | C | 1 | a0001c0001t0033g0258 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.274+18032T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553789 | ||||||
| chr10:28553824
|
G | A | 1 | a0001c0001t0155g0159 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.274+18067G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553824 | ||||||
| chr10:28553853
|
A | G | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.274+18096A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553853 | ||||||
| chr10:28553914
|
G | A | 3 | a0001c0001t0001g0175a0001c0001t0002g0210a0001c0001t0009g0176 | 3 | HG02155.hp2 NA18967.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.274+18157G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28553914 | ||||||
| chr10:28554093
|
C | T | 123 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(120): Show | 123 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.274+18336C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554093 | ||||||
| chr10:28554113
|
C | T | 2 | a0001c0001t0015g0198a0001c0001t0091g0179 | 2 | NA18994.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.274+18356C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554113 | ||||||
| chr10:28554194
|
A | G | 1 | a0001c0001t0020g0242 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.274+18437A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554194 | ||||||
| chr10:28554430
|
C | T | 4 | a0001c0001t0044g0093a0001c0001t0044g0095a0001c0001t0121g0262others(1): Show | 4 | HG02040.hp1 NA18965.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+18673C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554430 | ||||||
| chr10:28554483
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+18726A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554483 | ||||||
| chr10:28554532
|
A | G | 1 | a0001c0001t0150g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.274+18775A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554532 | ||||||
| chr10:28554549
|
G | A | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.274+18792G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554549 | ||||||
| chr10:28554577
|
G | GCCATGAT others(312): Show |
1 | a0001c0001t0039g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.274+18835_274+1883 others(323): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28554577 | |||||
| chr10:28554594
|
C | T | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+18837C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554594 | ||||||
| chr10:28554611
|
C | T | 2 | a0001c0001t0012g0221a0001c0005t0090g0220 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+18854C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554611 | ||||||
| chr10:28554717
|
A | G | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.274+18960A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554717 | ||||||
| chr10:28554857
|
G | T | 35 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(32): Show | 35 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.274+19100G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554857 | ||||||
| chr10:28554923
|
A | T | 1 | a0001c0001t0007g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274+19166A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554923 | ||||||
| chr10:28554925
|
T | C | 69 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.274+19168T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28554925 | ||||||
| chr10:28555004
|
G | C | 83 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(80): Show | 83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.274+19247G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555004 | ||||||
| chr10:28555014
|
G | A | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.274+19257G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555014 | ||||||
| chr10:28555160
|
T | A | 2 | a0001c0001t0040g0227a0001c0001t0040g0228 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.274+19403T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555160 | ||||||
| chr10:28555213
|
A | G | 1 | a0001c0001t0120g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.274+19456A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555213 | ||||||
| chr10:28555334
|
A | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+19577A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555334 | ||||||
| chr10:28555437
|
AT | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.274+19690delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28555437 | |||||
| chr10:28555465
|
G | A | 2 | a0001c0001t0005g0133a0001c0001t0005g0208 | 2 | HG00741.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.274+19708G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555465 | ||||||
| chr10:28555498
|
TGGTG | T | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+19744_274+1974 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28555498 | |||||
| chr10:28555506
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+19749G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555506 | ||||||
| chr10:28555513
|
G | A | 2 | a0001c0001t0040g0227a0001c0001t0040g0228 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.274+19756G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555513 | ||||||
| chr10:28555692
|
C | T | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+19935C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555692 | ||||||
| chr10:28555762
|
G | A | 6 | a0001c0001t0002g0168a0001c0001t0002g0204a0001c0001t0006g0119others(3): Show | 6 | HG00642.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+20005G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555762 | ||||||
| chr10:28555903
|
A | G | 4 | a0001c0001t0002g0180a0001c0001t0002g0202a0001c0001t0006g0116others(1): Show | 4 | HG01358.hp2 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+20146A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28555903 | ||||||
| chr10:28556229
|
CTT | C | 6 | a0001c0001t0012g0277a0001c0001t0018g0278a0001c0001t0018g0283others(3): Show | 6 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+20473_274+2047 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28556229 | ||||||
| chr10:28556312
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+20555A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28556312 | ||||||
| chr10:28556388
|
A | AT | 17 | a0001c0001t0001g0160a0001c0001t0002g0161a0001c0001t0005g0110others(14): Show | 17 | HG00140.hp1 HG01167.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.274+20658dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
A | ATT | 56 | a0001c0001t0001g0109a0001c0001t0001g0130a0001c0001t0001g0146others(53): Show | 56 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.274+20657_274+2065 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
A | ATTT | 43 | a0001c0001t0001g0126a0001c0001t0001g0140a0001c0001t0001g0153others(40): Show | 43 | HG00558.hp1 HG00735.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.274+20656_274+2065 others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
A | ATTTT | 9 | a0001c0001t0001g0067a0001c0001t0002g0138a0001c0001t0002g0210others(6): Show | 9 | HG00673.hp2 HG01257.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.274+20655_274+2065 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
A | ATTTTT | 17 | a0001c0001t0002g0213a0001c0001t0018g0283a0001c0001t0028g0285others(14): Show | 17 | HG00099.hp2 HG00735.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.274+20654_274+2065 others(9): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
A | ATTTTTT | 10 | a0001c0001t0004g0058a0001c0001t0006g0201a0001c0001t0007g0030others(7): Show | 10 | HG00280.hp2 HG00741.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.274+20653_274+2065 others(10): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
A | ATTTTTTT | 24 | a0001c0001t0007g0023a0001c0001t0007g0059a0001c0001t0008g0011others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.274+20652_274+2065 others(11): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
A | ATTTTTTT others(1): Show |
27 | a0001c0001t0004g0014a0001c0001t0004g0035a0001c0001t0004g0036others(24): Show | 27 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.274+20651_274+2065 others(12): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
A | ATTTTTTT others(2): Show |
14 | a0001c0001t0004g0026a0001c0001t0004g0029a0001c0001t0004g0045others(11): Show | 14 | HG00738.hp2 HG01175.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.274+20650_274+2065 others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
A | ATTTTTTT others(3): Show |
9 | a0001c0001t0008g0017a0001c0001t0008g0022a0001c0001t0045g0028others(6): Show | 9 | HG00673.hp1 HG00733.hp2 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.274+20649_274+2065 others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0050g0018 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.274+20648_274+2065 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
AT | A | 24 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0085others(21): Show | 24 | HG00597.hp1 HG00597.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.274+20658delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
ATT | A | 21 | a0001c0001t0003g0084a0001c0001t0003g0092a0001c0001t0003g0101others(18): Show | 21 | HG01496.hp1 HG01891.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.274+20657_274+2065 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0004g0031a0001c0001t0057g0139 | 2 | HG02080.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.274+20648_274+2065 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556388
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+20643_274+2065 others(20): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28556388 | |||||
| chr10:28556564
|
A | T | 1 | a0001c0001t0007g0025 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.274+20807A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28556564 | ||||||
| chr10:28556663
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+20906A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28556663 | ||||||
| chr10:28556866
|
G | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.274+21109G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28556866 | ||||||
| chr10:28557065
|
G | GT | 30 | a0001c0001t0004g0031a0001c0001t0008g0019a0001c0001t0012g0191others(27): Show | 30 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.274+21319dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28557065 | |||||
| chr10:28557065
|
G | GTT | 6 | a0001c0001t0012g0277a0001c0001t0018g0278a0001c0001t0018g0283others(3): Show | 6 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+21318_274+2131 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28557065 | |||||
| chr10:28557223
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+21466C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557223 | ||||||
| chr10:28557326
|
A | G | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+21569A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557326 | ||||||
| chr10:28557583
|
G | A | 224 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(221): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.274+21826G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557583 | ||||||
| chr10:28557617
|
C | G | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+21860C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557617 | ||||||
| chr10:28557652
|
C | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+21895C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557652 | ||||||
| chr10:28557740
|
G | T | 1 | a0001c0001t0043g0289 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.274+21983G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557740 | ||||||
| chr10:28557888
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+22131C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557888 | ||||||
| chr10:28557990
|
C | T | 1 | a0001c0001t0136g0060 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.274+22233C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557990 | ||||||
| chr10:28557993
|
G | A | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+22236G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28557993 | ||||||
| chr10:28558148
|
A | G | 123 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(120): Show | 123 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.274+22391A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558148 | ||||||
| chr10:28558239
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+22482A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558239 | ||||||
| chr10:28558342
|
A | G | 1 | a0001c0002t0013g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.274+22585A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558342 | ||||||
| chr10:28558371
|
C | A | 69 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(66): Show | 69 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.274+22614C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558371 | ||||||
| chr10:28558427
|
TG | T | 9 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(6): Show | 9 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.274+22673delG | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28558427 | |||||
| chr10:28558727
|
A | G | 1 | a0001c0001t0139g0046 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.274+22970A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558727 | ||||||
| chr10:28558753
|
C | G | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274+22996C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558753 | ||||||
| chr10:28558768
|
T | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+23011T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558768 | ||||||
| chr10:28558788
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.274+23031G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558788 | ||||||
| chr10:28558931
|
C | T | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.274+23174C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28558931 | ||||||
| chr10:28559050
|
G | A | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+23293G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559050 | ||||||
| chr10:28559100
|
A | G | 1 | a0001c0001t0145g0050 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.274+23343A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559100 | ||||||
| chr10:28559135
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0017g0134 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.274+23378_274+2337 others(18): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559135 | ||||||
| chr10:28559135
|
G | GGTGTGTG others(9): Show |
1 | a0001c0001t0006g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.274+23378_274+2337 others(20): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559135 | ||||||
| chr10:28559135
|
G | GGTGTGTG others(11): Show |
3 | a0001c0001t0001g0160a0001c0001t0002g0161a0001c0001t0009g0121 | 3 | HG02451.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.274+23378_274+2337 others(22): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559135 | ||||||
| chr10:28559135
|
G | GGTGTGTG others(15): Show |
1 | a0001c0001t0031g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.274+23378_274+2337 others(26): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559135 | ||||||
| chr10:28559135
|
GAT | G | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.274+23379_274+2338 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559135 | ||||||
| chr10:28559136
|
A | ATG | 26 | a0001c0001t0003g0076a0001c0001t0003g0085a0001c0001t0003g0091others(23): Show | 26 | HG00558.hp2 HG00621.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.274+23407_274+2340 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
A | ATGTG | 26 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0087others(23): Show | 26 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.274+23405_274+2340 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
A | ATGTGTG | 27 | a0001c0001t0012g0191a0001c0001t0012g0265a0001c0001t0012g0274others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.274+23403_274+2340 others(10): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
A | ATGTGTGT others(1): Show |
11 | a0001c0001t0022g0302a0001c0001t0028g0285a0001c0001t0028g0290others(8): Show | 11 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.274+23401_274+2340 others(12): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
A | ATGTGTGT others(3): Show |
8 | a0001c0001t0001g0153a0001c0001t0005g0133a0001c0001t0005g0208others(5): Show | 8 | HG00558.hp1 HG00741.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.274+23399_274+2340 others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
A | ATGTGTGT others(5): Show |
26 | a0001c0001t0001g0186a0001c0001t0002g0132a0001c0001t0002g0151others(23): Show | 26 | HG01243.hp1 HG01243.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.274+23397_274+2340 others(16): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
A | ATGTGTGT others(7): Show |
34 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0002g0168others(31): Show | 34 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.274+23395_274+2340 others(18): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
A | ATGTGTGT others(9): Show |
40 | a0001c0001t0001g0158a0001c0001t0001g0170a0001c0001t0001g0171others(37): Show | 40 | HG00639.hp2 HG00735.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.274+23393_274+2340 others(20): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
A | ATGTGTGT others(11): Show |
13 | a0001c0001t0001g0126a0001c0001t0001g0140a0001c0001t0001g0197others(10): Show | 13 | HG01255.hp1 HG01884.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.274+23391_274+2340 others(22): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
A | ATGTGTGT others(13): Show |
6 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0217others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+23389_274+2340 others(24): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
A | ATGTGTGT others(15): Show |
2 | a0001c0001t0005g0212a0001c0001t0103g0194 | 2 | HG01934.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.274+23387_274+2340 others(26): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
A | ATTGTGTG others(6): Show |
1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.274+23380_274+2338 others(17): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
A | G | 6 | a0001c0001t0001g0160a0001c0001t0002g0161a0001c0001t0006g0115others(3): Show | 6 | HG01081.hp1 HG02451.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+23379A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559136 | ||||||
| chr10:28559136
|
ATG | A | 3 | a0001c0001t0034g0260a0001c0001t0067g0269a0001c0001t0127g0261 | 3 | HG01256.hp2 HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.274+23407_274+2340 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559136
|
ATGTGTGT others(5): Show |
A | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.274+23397_274+2340 others(16): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28559136 | |||||
| chr10:28559166
|
A | G | 4 | a0001c0001t0021g0002a0001c0001t0021g0304a0001c0001t0022g0002others(1): Show | 4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+23409A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559166 | ||||||
| chr10:28559167
|
A | T | 4 | a0001c0001t0021g0002a0001c0001t0021g0304a0001c0001t0022g0002others(1): Show | 4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+23410A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559167 | ||||||
| chr10:28559170
|
C | G | 4 | a0001c0001t0021g0002a0001c0001t0021g0304a0001c0001t0022g0002others(1): Show | 4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+23413C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559170 | ||||||
| chr10:28559172
|
G | GTGTGTAA others(2): Show |
3 | a0001c0001t0021g0002a0001c0001t0021g0304a0001c0001t0022g0002 | 3 | HG01106.hp2 HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.274+23415_274+2341 others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559172 | ||||||
| chr10:28559172
|
G | GTGTGTGT others(4): Show |
1 | a0001c0001t0042g0305 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.274+23415_274+2341 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559172 | ||||||
| chr10:28559173
|
A | C | 4 | a0001c0001t0021g0002a0001c0001t0021g0304a0001c0001t0022g0002others(1): Show | 4 | HG01106.hp2 HG01884.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+23416A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559173 | ||||||
| chr10:28559399
|
T | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.274+23642T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559399 | ||||||
| chr10:28559718
|
T | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-23681T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559718 | ||||||
| chr10:28559774
|
A | T | 1 | a0001c0001t0105g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.275-23625A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559774 | ||||||
| chr10:28559855
|
G | C | 1 | a0001c0001t0085g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.275-23544G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559855 | ||||||
| chr10:28559860
|
A | G | 50 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0130others(47): Show | 50 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.275-23539A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559860 | ||||||
| chr10:28559874
|
G | A | 1 | a0001c0001t0028g0290 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.275-23525G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28559874 | ||||||
| chr10:28560073
|
G | A | 2 | a0001c0001t0008g0011a0001c0001t0045g0012 | 2 | HG00280.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.275-23326G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560073 | ||||||
| chr10:28560094
|
C | T | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-23305C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560094 | ||||||
| chr10:28560111
|
A | G | 288 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.275-23288A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560111 | ||||||
| chr10:28560273
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.275-23126A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560273 | ||||||
| chr10:28560397
|
C | T | 1 | a0001c0001t0024g0099 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.275-23002C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560397 | ||||||
| chr10:28560398
|
G | A | 1 | a0001c0001t0120g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.275-23001G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560398 | ||||||
| chr10:28560496
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-22903C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560496 | ||||||
| chr10:28560534
|
A | T | 1 | a0001c0001t0055g0184 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.275-22865A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560534 | ||||||
| chr10:28560621
|
A | G | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.275-22778A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28560621 | ||||||
| chr10:28561003
|
G | A | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.275-22396G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561003 | ||||||
| chr10:28561319
|
A | G | 1 | a0001c0001t0014g0215 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.275-22080A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561319 | ||||||
| chr10:28561328
|
C | G | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.275-22071C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561328 | ||||||
| chr10:28561371
|
T | C | 1 | a0001c0001t0065g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.275-22028T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561371 | ||||||
| chr10:28561497
|
G | GT | 59 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.275-21892dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28561497 | |||||
| chr10:28561539
|
C | T | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-21860C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561539 | ||||||
| chr10:28561577
|
G | C | 1 | a0001c0001t0039g0252 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.275-21822G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561577 | ||||||
| chr10:28561649
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-21750G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561649 | ||||||
| chr10:28561652
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-21747G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561652 | ||||||
| chr10:28561654
|
C | T | 1 | a0001c0001t0033g0258 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.275-21745C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561654 | ||||||
| chr10:28561682
|
C | G | 1 | a0001c0001t0102g0280 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.275-21717C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561682 | ||||||
| chr10:28561823
|
T | C | 1 | a0001c0001t0098g0157 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.275-21576T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28561823 | ||||||
| chr10:28562025
|
T | C | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.275-21374T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562025 | ||||||
| chr10:28562026
|
G | C | 1 | a0001c0001t0133g0051 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.275-21373G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562026 | ||||||
| chr10:28562267
|
G | A | 155 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.275-21132G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562267 | ||||||
| chr10:28562313
|
C | T | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-21086C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562313 | ||||||
| chr10:28562423
|
T | G | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-20976T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562423 | ||||||
| chr10:28562633
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-20766G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562633 | ||||||
| chr10:28562794
|
G | A | 1 | a0001c0001t0149g0291 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.275-20605G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562794 | ||||||
| chr10:28562908
|
G | A | 1 | a0001c0001t0113g0127 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.275-20491G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28562908 | ||||||
| chr10:28563175
|
GA | G | 6 | a0001c0001t0007g0023a0001c0001t0007g0030a0001c0001t0007g0042others(3): Show | 6 | NA18948.hp1 NA18955.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-20223delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28563175 | ||||||
| chr10:28563497
|
T | C | 1 | a0001c0001t0015g0181 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.275-19902T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28563497 | ||||||
| chr10:28563625
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.275-19774G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28563625 | ||||||
| chr10:28563744
|
C | CT | 58 | a0001c0001t0001g0126a0001c0001t0001g0158a0001c0001t0001g0197others(55): Show | 58 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.275-19626dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
C | CTT | 43 | a0001c0001t0001g0130a0001c0001t0002g0132a0001c0001t0003g0084others(40): Show | 43 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.275-19627_275-1962 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
C | CTTT | 28 | a0001c0001t0001g0067a0001c0001t0001g0153a0001c0001t0001g0186others(25): Show | 28 | HG00558.hp1 HG00735.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.275-19628_275-1962 others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
C | CTTTT | 11 | a0001c0001t0001g0109a0001c0001t0001g0140a0001c0001t0002g0138others(8): Show | 11 | HG01255.hp1 HG01934.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.275-19629_275-1962 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
C | CTTTTTTT | 19 | a0001c0001t0004g0029a0001c0001t0004g0036a0001c0001t0004g0045others(16): Show | 19 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.275-19632_275-1962 others(11): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
C | CTTTTTTT others(1): Show |
17 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0058others(14): Show | 17 | HG00673.hp1 HG00733.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.275-19633_275-1962 others(12): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
C | CTTTTTTT others(2): Show |
14 | a0001c0001t0004g0031a0001c0001t0004g0035a0001c0001t0007g0062others(11): Show | 14 | HG00609.hp2 HG00621.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.275-19634_275-1962 others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0066g0044a0001c0001t0135g0034a0001c0001t0147g0033 | 3 | HG02132.hp2 NA19085.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.275-19635_275-1962 others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0007g0023a0001c0001t0136g0060a0001c0001t0145g0050 | 3 | HG01515.hp2 HG02293.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.275-19636_275-1962 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0007g0042 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.275-19637_275-1962 others(16): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0045g0028 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.275-19639_275-1962 others(18): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
CT | C | 9 | a0001c0001t0011g0318a0001c0001t0021g0292a0001c0001t0027g0297others(6): Show | 9 | HG00609.hp1 HG01168.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.275-19626delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
CTTTTTTT others(2): Show |
C | 12 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0002t0013g0003others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.275-19634_275-1962 others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0123g0088 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.275-19636_275-1962 others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563744
|
CTTTTTTT others(6): Show |
C | 28 | a0001c0001t0006g0115a0001c0001t0012g0191a0001c0001t0012g0265others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.275-19638_275-1962 others(17): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28563744 | |||||
| chr10:28563774
|
G | T | 2 | a0001c0001t0008g0011a0001c0001t0045g0012 | 2 | HG00280.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.275-19625G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28563774 | ||||||
| chr10:28563842
|
C | T | 1 | a0001c0001t0112g0163 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.275-19557C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28563842 | ||||||
| chr10:28563874
|
A | C | 220 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(217): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.275-19525A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28563874 | ||||||
| chr10:28564382
|
G | A | 2 | a0001c0001t0040g0227a0001c0001t0040g0228 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.275-19017G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564382 | ||||||
| chr10:28564620
|
T | C | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.275-18779T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564620 | ||||||
| chr10:28564841
|
T | A | 1 | a0001c0002t0013g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.275-18558T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564841 | ||||||
| chr10:28564864
|
T | G | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.275-18535T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564864 | ||||||
| chr10:28564894
|
T | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-18505T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564894 | ||||||
| chr10:28564907
|
G | T | 3 | a0002c0003t0026g0068a0002c0003t0026g0229a0002c0003t0041g0230 | 3 | HG02723.hp2 HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.275-18492G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564907 | ||||||
| chr10:28564927
|
C | T | 1 | a0001c0001t0030g0149 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.275-18472C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564927 | ||||||
| chr10:28564933
|
G | A | 288 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.275-18466G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28564933 | ||||||
| chr10:28565010
|
C | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-18389C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28565010 | ||||||
| chr10:28565106
|
CT | C | 297 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.275-18286delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28565106 | |||||
| chr10:28565153
|
T | C | 3 | a0001c0004t0069g0182a0001c0004t0078g0128a0001c0004t0079g0195 | 3 | HG01069.hp1 HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.275-18246T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28565153 | ||||||
| chr10:28565185
|
C | A | 283 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.275-18214C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28565185 | ||||||
| chr10:28565186
|
C | T | 1 | a0001c0001t0033g0258 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.275-18213C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28565186 | ||||||
| chr10:28565605
|
A | G | 1 | a0001c0001t0107g0232 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.275-17794A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28565605 | ||||||
| chr10:28565711
|
A | G | 203 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.275-17688A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28565711 | ||||||
| chr10:28566063
|
C | T | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.275-17336C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28566063 | ||||||
| chr10:28566166
|
A | G | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.275-17233A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28566166 | ||||||
| chr10:28566167
|
C | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-17232C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28566167 | ||||||
| chr10:28566386
|
A | T | 3 | a0001c0001t0034g0260a0001c0001t0067g0269a0001c0001t0127g0261 | 3 | HG01256.hp2 HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.275-17013A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28566386 | ||||||
| chr10:28566507
|
C | T | 1 | a0001c0001t0003g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.275-16892C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28566507 | ||||||
| chr10:28566872
|
A | C | 2 | a0001c0001t0040g0227a0001c0001t0040g0228 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.275-16527A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28566872 | ||||||
| chr10:28566952
|
G | GT | 62 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.275-16434dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28566952 | |||||
| chr10:28567090
|
A | G | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.275-16309A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567090 | ||||||
| chr10:28567214
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0002g0161 | 2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.275-16185C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567214 | ||||||
| chr10:28567399
|
C | T | 1 | a0001c0001t0066g0044 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.275-16000C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567399 | ||||||
| chr10:28567523
|
A | T | 1 | a0001c0001t0002g0151 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.275-15876A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567523 | ||||||
| chr10:28567610
|
A | G | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.275-15789A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567610 | ||||||
| chr10:28567808
|
G | A | 1 | a0001c0001t0007g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.275-15591G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567808 | ||||||
| chr10:28567890
|
G | A | 121 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(118): Show | 121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.275-15509G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567890 | ||||||
| chr10:28567914
|
C | T | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-15485C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28567914 | ||||||
| chr10:28568001
|
G | A | 2 | a0001c0001t0005g0133a0001c0001t0005g0208 | 2 | HG00741.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.275-15398G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568001 | ||||||
| chr10:28568082
|
G | A | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-15317G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568082 | ||||||
| chr10:28568204
|
T | C | 36 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(33): Show | 36 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.275-15195T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568204 | ||||||
| chr10:28568249
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-15150C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568249 | ||||||
| chr10:28568385
|
G | T | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.275-15014G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568385 | ||||||
| chr10:28568444
|
G | A | 3 | a0001c0001t0033g0309a0001c0001t0059g0106a0001c0001t0119g0308 | 3 | HG02895.hp1 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.275-14955G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568444 | ||||||
| chr10:28568445
|
G | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.275-14954G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568445 | ||||||
| chr10:28568521
|
C | T | 3 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0010g0080 | 3 | NA18971.hp1 NA18972.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.275-14878C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568521 | ||||||
| chr10:28568531
|
C | T | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.275-14868C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568531 | ||||||
| chr10:28568814
|
C | T | 15 | a0001c0001t0004g0029a0001c0001t0004g0036a0001c0001t0007g0025others(12): Show | 15 | HG00735.hp2 HG01069.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.275-14585C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568814 | ||||||
| chr10:28568825
|
G | A | 1 | a0001c0001t0021g0292 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.275-14574G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568825 | ||||||
| chr10:28568878
|
C | G | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-14521C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568878 | ||||||
| chr10:28568886
|
A | G | 18 | a0001c0001t0012g0265a0001c0001t0012g0274a0001c0001t0018g0257others(15): Show | 18 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.275-14513A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568886 | ||||||
| chr10:28568931
|
A | G | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.275-14468A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568931 | ||||||
| chr10:28568958
|
A | G | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-14441A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568958 | ||||||
| chr10:28568991
|
A | G | 3 | a0001c0001t0061g0268a0001c0001t0093g0178a0001c0001t0094g0167 | 3 | HG02922.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.275-14408A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28568991 | ||||||
| chr10:28569534
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0030g0218a0001c0001t0080g0131 | 3 | HG01346.hp1 HG03831.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.275-13865G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569534 | ||||||
| chr10:28569628
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-13771G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569628 | ||||||
| chr10:28569649
|
C | T | 204 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.275-13750C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569649 | ||||||
| chr10:28569813
|
T | A | 1 | a0001c0001t0039g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.275-13586T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569813 | ||||||
| chr10:28569904
|
AT | A | 3 | a0001c0001t0016g0141a0001c0001t0016g0183a0001c0001t0053g0107 | 3 | NA18964.hp2 NA18972.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.275-13492delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28569904 | |||||
| chr10:28569915
|
C | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-13484C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569915 | ||||||
| chr10:28569960
|
C | T | 59 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.275-13439C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569960 | ||||||
| chr10:28569971
|
C | T | 9 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(6): Show | 9 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.275-13428C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28569971 | ||||||
| chr10:28570050
|
A | T | 288 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.275-13349A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570050 | ||||||
| chr10:28570063
|
G | A | 204 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.275-13336G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570063 | ||||||
| chr10:28570150
|
C | T | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.275-13249C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570150 | ||||||
| chr10:28570380
|
G | T | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.275-13019G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570380 | ||||||
| chr10:28570383
|
A | G | 1 | a0001c0001t0126g0226 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.275-13016A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570383 | ||||||
| chr10:28570389
|
C | A | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-13010C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570389 | ||||||
| chr10:28570431
|
C | G | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.275-12968C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570431 | ||||||
| chr10:28570435
|
C | G | 2 | a0001c0001t0137g0038a0001c0001t0138g0032 | 2 | NA18978.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.275-12964C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570435 | ||||||
| chr10:28570626
|
T | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-12773T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570626 | ||||||
| chr10:28570633
|
A | G | 5 | a0001c0001t0026g0231a0002c0003t0026g0068a0002c0003t0026g0229others(2): Show | 5 | HG01123.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-12766A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570633 | ||||||
| chr10:28570643
|
T | C | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-12756T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570643 | ||||||
| chr10:28570889
|
A | G | 1 | a0001c0001t0073g0137 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.275-12510A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570889 | ||||||
| chr10:28570926
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.275-12473G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28570926 | ||||||
| chr10:28570946
|
CT | C | 12 | a0001c0001t0004g0029a0001c0001t0004g0054a0001c0001t0004g0314others(9): Show | 12 | HG01358.hp1 HG01978.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.275-12425delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | |||||
| chr10:28570946
|
CTT | C | 45 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0031others(42): Show | 45 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.275-12426_275-1242 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | |||||
| chr10:28570946
|
CTTT | C | 35 | a0001c0001t0001g0171a0001c0001t0002g0210a0001c0001t0003g0092others(32): Show | 35 | HG00673.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.275-12427_275-1242 others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | |||||
| chr10:28570946
|
CTTTT | C | 166 | a0001c0001t0001g0109a0001c0001t0001g0126a0001c0001t0001g0130others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.275-12428_275-1242 others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | |||||
| chr10:28570946
|
CTTTTT | C | 8 | a0001c0001t0001g0067a0001c0001t0005g0169a0001c0001t0006g0069others(5): Show | 8 | HG00639.hp2 HG01257.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-12429_275-1242 others(9): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | |||||
| chr10:28570946
|
CTTTTTTT others(2): Show |
C | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.275-12433_275-1242 others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | |||||
| chr10:28570946
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0012g0277a0001c0001t0023g0070a0001c0001t0023g0254others(2): Show | 5 | HG00280.hp2 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-12434_275-1242 others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28570946 | |||||
| chr10:28571076
|
C | T | 1 | a0001c0001t0066g0044 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.275-12323C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571076 | ||||||
| chr10:28571147
|
C | T | 1 | a0001c0002t0013g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.275-12252C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571147 | ||||||
| chr10:28571161
|
C | T | 1 | a0001c0001t0129g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.275-12238C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571161 | ||||||
| chr10:28571171
|
C | T | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-12228C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571171 | ||||||
| chr10:28571195
|
G | A | 3 | a0001c0001t0007g0059a0001c0001t0008g0048a0001c0001t0146g0047 | 3 | HG00099.hp1 HG00323.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.275-12204G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571195 | ||||||
| chr10:28571254
|
T | G | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-12145T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571254 | ||||||
| chr10:28571289
|
C | T | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.275-12110C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571289 | ||||||
| chr10:28571525
|
C | T | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.275-11874C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571525 | ||||||
| chr10:28571635
|
C | G | 1 | a0001c0001t0003g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.275-11764C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571635 | ||||||
| chr10:28571635
|
C | T | 1 | a0001c0001t0012g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.275-11764C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571635 | ||||||
| chr10:28571830
|
A | G | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-11569A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571830 | ||||||
| chr10:28571901
|
T | C | 1 | a0001c0001t0005g0118 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.275-11498T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28571901 | ||||||
| chr10:28572013
|
G | T | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-11386G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572013 | ||||||
| chr10:28572036
|
C | T | 1 | a0001c0001t0103g0194 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.275-11363C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572036 | ||||||
| chr10:28572173
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-11226C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572173 | ||||||
| chr10:28572174
|
TA | T | 203 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.275-11221delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28572174 | |||||
| chr10:28572291
|
C | T | 1 | a0001c0001t0026g0231 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.275-11108C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572291 | ||||||
| chr10:28572337
|
C | CA | 96 | a0001c0001t0002g0219a0001c0001t0003g0076a0001c0001t0003g0084others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.275-11045dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28572337 | |||||
| chr10:28572337
|
C | CAA | 10 | a0001c0001t0003g0083a0001c0001t0003g0101a0001c0001t0019g0271others(7): Show | 10 | HG01192.hp2 HG01928.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.275-11046_275-1104 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28572337 | |||||
| chr10:28572337
|
CA | C | 13 | a0001c0001t0002g0213a0001c0001t0017g0190a0001c0001t0026g0231others(10): Show | 13 | HG01123.hp2 HG02004.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.275-11045delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28572337 | |||||
| chr10:28572365
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.275-11034A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572365 | ||||||
| chr10:28572464
|
G | C | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.275-10935G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572464 | ||||||
| chr10:28572548
|
A | T | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.275-10851A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572548 | ||||||
| chr10:28572799
|
G | A | 4 | a0002c0003t0026g0068a0002c0003t0026g0229a0002c0003t0041g0223others(1): Show | 4 | HG01123.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-10600G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572799 | ||||||
| chr10:28572833
|
A | T | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-10566A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28572833 | ||||||
| chr10:28573118
|
A | AT | 136 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0130others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.275-10272dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28573118 | |||||
| chr10:28573118
|
A | ATT | 151 | a0001c0001t0001g0126a0001c0001t0001g0158a0001c0001t0001g0160others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.275-10273_275-1027 others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28573118 | |||||
| chr10:28573172
|
C | G | 1 | a0001c0001t0085g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.275-10227C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573172 | ||||||
| chr10:28573212
|
T | G | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.275-10187T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573212 | ||||||
| chr10:28573223
|
C | T | 67 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.275-10176C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573223 | ||||||
| chr10:28573259
|
C | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-10140C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573259 | ||||||
| chr10:28573332
|
C | G | 1 | a0001c0001t0012g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.275-10067C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573332 | ||||||
| chr10:28573339
|
C | T | 8 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(5): Show | 8 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-10060C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573339 | ||||||
| chr10:28573360
|
T | A | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-10039T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573360 | ||||||
| chr10:28573583
|
C | T | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-9816C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573583 | ||||||
| chr10:28573746
|
A | G | 1 | a0001c0001t0120g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.275-9653A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573746 | ||||||
| chr10:28573866
|
C | G | 3 | a0001c0001t0037g0247a0001c0001t0065g0225a0001c0001t0125g0246 | 3 | HG00438.hp2 NA18612.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.275-9533C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573866 | ||||||
| chr10:28573926
|
A | G | 1 | a0002c0003t0041g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.275-9473A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573926 | ||||||
| chr10:28573977
|
C | G | 1 | a0001c0001t0091g0179 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.275-9422C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28573977 | ||||||
| chr10:28574026
|
T | A | 1 | a0001c0001t0103g0194 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.275-9373T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574026 | ||||||
| chr10:28574112
|
GTTTTTA | G | 120 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(117): Show | 120 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.275-9281_275-9276d others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28574112 | |||||
| chr10:28574117
|
T | C | 1 | a0001c0001t0004g0014 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.275-9282T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574117 | ||||||
| chr10:28574216
|
C | T | 3 | a0001c0001t0008g0017a0001c0001t0045g0028a0001c0001t0050g0018 | 3 | HG00609.hp2 NA18962.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.275-9183C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574216 | ||||||
| chr10:28574230
|
C | T | 1 | a0001c0002t0035g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.275-9169C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574230 | ||||||
| chr10:28574381
|
C | T | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-9018C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574381 | ||||||
| chr10:28574383
|
G | A | 22 | a0001c0001t0004g0054a0001c0001t0004g0058a0001c0001t0004g0314others(19): Show | 22 | HG00280.hp1 HG00621.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.275-9016G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574383 | ||||||
| chr10:28574443
|
C | A | 1 | a0001c0001t0028g0290 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.275-8956C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574443 | ||||||
| chr10:28574444
|
G | A | 35 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(32): Show | 35 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.275-8955G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574444 | ||||||
| chr10:28574605
|
G | C | 1 | a0001c0001t0091g0179 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.275-8794G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574605 | ||||||
| chr10:28574642
|
C | G | 4 | a0002c0003t0026g0068a0002c0003t0026g0229a0002c0003t0041g0223others(1): Show | 4 | HG01123.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-8757C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574642 | ||||||
| chr10:28574736
|
G | A | 1 | a0001c0001t0142g0016 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.275-8663G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574736 | ||||||
| chr10:28574758
|
A | G | 3 | a0001c0001t0004g0014a0001c0001t0049g0039a0001c0001t0128g0015 | 3 | HG03831.hp1 HG04204.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.275-8641A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574758 | ||||||
| chr10:28574867
|
T | C | 7 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0006g0122others(4): Show | 7 | NA18969.hp1 NA18984.hp1 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.275-8532T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574867 | ||||||
| chr10:28574879
|
C | G | 121 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(118): Show | 121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.275-8520C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574879 | ||||||
| chr10:28574923
|
G | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-8476G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574923 | ||||||
| chr10:28574954
|
G | C | 1 | a0001c0001t0038g0248 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.275-8445G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574954 | ||||||
| chr10:28574958
|
C | G | 1 | a0001c0001t0105g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.275-8441C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574958 | ||||||
| chr10:28574960
|
A | G | 1 | a0001c0001t0003g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.275-8439A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28574960 | ||||||
| chr10:28574986
|
TG | T | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.275-8411delG | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28574986 | |||||
| chr10:28575026
|
G | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.275-8373G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575026 | ||||||
| chr10:28575058
|
T | G | 36 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(33): Show | 36 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.275-8341T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575058 | ||||||
| chr10:28575244
|
C | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-8155C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575244 | ||||||
| chr10:28575777
|
G | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.275-7622G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575777 | ||||||
| chr10:28575782
|
G | T | 59 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.275-7617G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575782 | ||||||
| chr10:28575818
|
C | T | 6 | a0001c0001t0015g0198a0001c0001t0017g0120a0001c0001t0032g0216others(3): Show | 6 | HG00673.hp2 HG01975.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-7581C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575818 | ||||||
| chr10:28575826
|
C | T | 1 | a0001c0001t0008g0024 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.275-7573C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28575826 | ||||||
| chr10:28576118
|
C | T | 1 | a0001c0001t0006g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.275-7281C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28576118 | ||||||
| chr10:28576443
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-6956C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28576443 | ||||||
| chr10:28576600
|
G | T | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-6799G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28576600 | ||||||
| chr10:28576813
|
T | C | 2 | a0001c0001t0001g0171a0001c0001t0005g0172 | 2 | HG01192.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.275-6586T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28576813 | ||||||
| chr10:28576911
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-6488A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28576911 | ||||||
| chr10:28577325
|
G | GT | 6 | a0001c0001t0004g0058a0001c0001t0010g0272a0001c0001t0011g0243others(3): Show | 6 | HG01167.hp2 HG02056.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-6066dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28577325 | |||||
| chr10:28577407
|
A | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-5992A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28577407 | ||||||
| chr10:28577449
|
A | G | 1 | a0001c0001t0043g0289 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.275-5950A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28577449 | ||||||
| chr10:28577683
|
A | G | 1 | a0001c0001t0065g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.275-5716A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28577683 | ||||||
| chr10:28577764
|
C | T | 1 | a0001c0001t0120g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.275-5635C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28577764 | ||||||
| chr10:28577779
|
A | G | 6 | a0001c0001t0012g0277a0001c0001t0018g0278a0001c0001t0018g0283others(3): Show | 6 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-5620A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28577779 | ||||||
| chr10:28577949
|
G | A | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-5450G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28577949 | ||||||
| chr10:28578031
|
T | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-5368T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578031 | ||||||
| chr10:28578155
|
TCAAAA | T | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-5228_275-5224d others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28578155 | |||||
| chr10:28578284
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-5115A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578284 | ||||||
| chr10:28578291
|
C | G | 121 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(118): Show | 121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.275-5108C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578291 | ||||||
| chr10:28578293
|
T | G | 1 | a0001c0001t0015g0154 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.275-5106T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578293 | ||||||
| chr10:28578406
|
A | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-4993A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578406 | ||||||
| chr10:28578468
|
C | T | 59 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.275-4931C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578468 | ||||||
| chr10:28578711
|
C | A | 2 | a0001c0001t0008g0048a0001c0001t0146g0047 | 2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.275-4688C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578711 | ||||||
| chr10:28578818
|
T | C | 1 | a0001c0001t0008g0017 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.275-4581T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28578818 | ||||||
| chr10:28579014
|
C | G | 15 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0087others(12): Show | 15 | HG00597.hp1 HG02056.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.275-4385C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579014 | ||||||
| chr10:28579026
|
A | G | 155 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.275-4373A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579026 | ||||||
| chr10:28579074
|
C | G | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-4325C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579074 | ||||||
| chr10:28579174
|
A | AT | 45 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(42): Show | 45 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.275-4210dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28579174 | |||||
| chr10:28579174
|
AT | A | 25 | a0001c0001t0001g0160a0001c0001t0012g0191a0001c0001t0021g0002others(22): Show | 25 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.275-4210delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28579174 | |||||
| chr10:28579248
|
G | A | 1 | a0001c0001t0070g0275 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.275-4151G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579248 | ||||||
| chr10:28579474
|
G | C | 1 | a0001c0001t0001g0130 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.275-3925G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579474 | ||||||
| chr10:28579630
|
G | A | 1 | a0001c0001t0008g0017 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.275-3769G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579630 | ||||||
| chr10:28579685
|
ACAAT | A | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-3711_275-3708d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28579685 | |||||
| chr10:28579699
|
C | G | 1 | a0001c0001t0049g0061 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.275-3700C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579699 | ||||||
| chr10:28579734
|
T | C | 8 | a0001c0001t0001g0175a0001c0001t0002g0174a0001c0001t0002g0180others(5): Show | 8 | HG01358.hp2 HG01928.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.275-3665T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579734 | ||||||
| chr10:28579892
|
T | C | 204 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.275-3507T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28579892 | ||||||
| chr10:28579973
|
TGTTA | T | 62 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0130others(59): Show | 62 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.275-3422_275-3419d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28579973 | |||||
| chr10:28580056
|
A | C | 1 | a0001c0001t0023g0070 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.275-3343A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580056 | ||||||
| chr10:28580254
|
CT | C | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.275-3144delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580254 | ||||||
| chr10:28580255
|
T | C | 284 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.275-3144T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580255 | ||||||
| chr10:28580352
|
A | G | 1 | a0001c0001t0014g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.275-3047A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580352 | ||||||
| chr10:28580357
|
G | A | 1 | a0001c0001t0030g0218 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.275-3042G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580357 | ||||||
| chr10:28580611
|
T | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-2788T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580611 | ||||||
| chr10:28580749
|
T | C | 1 | a0001c0001t0105g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.275-2650T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580749 | ||||||
| chr10:28580800
|
T | C | 26 | a0001c0001t0012g0191a0001c0001t0012g0265a0001c0001t0012g0274others(23): Show | 26 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.275-2599T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580800 | ||||||
| chr10:28580922
|
A | T | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.275-2477A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28580922 | ||||||
| chr10:28581238
|
C | CT | 6 | a0001c0001t0011g0241a0001c0001t0011g0243a0001c0001t0025g0224others(3): Show | 6 | HG00558.hp2 HG00621.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-2129dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | |||||
| chr10:28581238
|
CT | C | 10 | a0001c0001t0011g0249a0001c0001t0025g0233a0001c0001t0037g0247others(7): Show | 10 | HG00438.hp2 HG00733.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.275-2129delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | |||||
| chr10:28581238
|
CTTTTTT | C | 18 | a0001c0001t0001g0140a0001c0001t0001g0158a0001c0001t0003g0083others(15): Show | 18 | HG00741.hp1 HG01167.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.275-2134_275-2129d others(8): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | |||||
| chr10:28581238
|
CTTTTTTT | C | 219 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0130others(216): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.275-2135_275-2129d others(9): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | |||||
| chr10:28581238
|
CTTTTTTT others(1): Show |
C | 37 | a0001c0001t0001g0126a0001c0001t0003g0087a0001c0001t0006g0069others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.275-2136_275-2129d others(10): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | |||||
| chr10:28581238
|
CTTTTTTT others(2): Show |
C | 8 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(5): Show | 8 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-2137_275-2129d others(11): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | |||||
| chr10:28581238
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0013g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.275-2138_275-2129d others(12): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | |||||
| chr10:28581238
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0008g0055 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.275-2140_275-2129d others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | |||||
| chr10:28581238
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0018g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.275-2144_275-2129d others(18): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | |||||
| chr10:28581238
|
CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0009g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.275-2148_275-2129d others(22): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28581238 | |||||
| chr10:28581254
|
T | C | 1 | a0001c0001t0115g0152 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.275-2145T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581254 | ||||||
| chr10:28581369
|
C | T | 3 | a0001c0001t0048g0063a0001c0001t0145g0050a0001c0001t0150g0065 | 3 | HG01109.hp2 HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.275-2030C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581369 | ||||||
| chr10:28581561
|
T | G | 123 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(120): Show | 123 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.275-1838T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581561 | ||||||
| chr10:28581573
|
G | C | 2 | a0001c0002t0035g0009a0001c0002t0096g0004 | 2 | HG00735.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.275-1826G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581573 | ||||||
| chr10:28581636
|
A | C | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.275-1763A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581636 | ||||||
| chr10:28581636
|
A | G | 1 | a0001c0001t0120g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.275-1763A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581636 | ||||||
| chr10:28581823
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275-1576A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28581823 | ||||||
| chr10:28582013
|
T | C | 1 | a0001c0002t0013g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.275-1386T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28582013 | ||||||
| chr10:28582316
|
A | T | 18 | a0001c0001t0012g0265a0001c0001t0012g0274a0001c0001t0018g0257others(15): Show | 18 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.275-1083A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28582316 | ||||||
| chr10:28582356
|
T | TA | 3 | a0001c0001t0015g0198a0001c0001t0017g0120a0001c0001t0091g0179 | 3 | HG01975.hp1 NA18994.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.275-1042dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 28582356 | |||||
| chr10:28582378
|
A | C | 1 | a0001c0001t0150g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.275-1021A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28582378 | ||||||
| chr10:28582387
|
A | G | 1 | a0001c0001t0059g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.275-1012A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28582387 | ||||||
| chr10:28582963
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.275-436G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 3/13 | chr10 | 28582963 | ||||||
| chr10:28583552
|
C | A | 1 | a0001c0001t0032g0216 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.381+47C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583552 | ||||||
| chr10:28583552
|
C | CA | 215 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(212): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.381+63dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 28583552 | |||||
| chr10:28583552
|
C | CAA | 11 | a0001c0001t0002g0138a0001c0001t0002g0144a0001c0001t0002g0202others(8): Show | 11 | HG00438.hp1 HG01256.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.381+62_381+63dupAA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 28583552 | |||||
| chr10:28583611
|
T | A | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+106T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583611 | ||||||
| chr10:28583612
|
T | A | 6 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(3): Show | 6 | HG02109.hp1 HG02129.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+107T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583612 | ||||||
| chr10:28583627
|
C | T | 6 | a0001c0002t0013g0003a0001c0002t0013g0007a0001c0002t0013g0008others(3): Show | 6 | HG00735.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+122C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583627 | ||||||
| chr10:28583666
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+161A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583666 | ||||||
| chr10:28583707
|
G | C | 2 | a0001c0001t0005g0133a0001c0001t0005g0208 | 2 | HG00741.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.381+202G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583707 | ||||||
| chr10:28583829
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+324G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28583829 | ||||||
| chr10:28583875
|
CATTT | C | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+374_381+377del others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 28583875 | |||||
| chr10:28584273
|
C | T | 121 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(118): Show | 121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.381+768C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584273 | ||||||
| chr10:28584276
|
G | A | 204 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.381+771G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584276 | ||||||
| chr10:28584301
|
A | G | 1 | a0001c0001t0008g0022 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.381+796A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584301 | ||||||
| chr10:28584548
|
T | A | 1 | a0001c0001t0108g0301 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.381+1043T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584548 | ||||||
| chr10:28584584
|
T | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+1079T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584584 | ||||||
| chr10:28584624
|
A | G | 1 | a0001c0001t0002g0124 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.381+1119A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584624 | ||||||
| chr10:28584634
|
C | T | 1 | a0001c0001t0142g0016 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.381+1129C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584634 | ||||||
| chr10:28584670
|
C | T | 5 | a0001c0001t0002g0124a0001c0001t0012g0221a0001c0001t0012g0222others(2): Show | 5 | HG01891.hp2 NA18969.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+1165C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28584670 | ||||||
| chr10:28585172
|
C | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+1667C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585172 | ||||||
| chr10:28585262
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+1757A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585262 | ||||||
| chr10:28585297
|
A | G | 203 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.381+1792A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585297 | ||||||
| chr10:28585331
|
G | T | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.381+1826G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585331 | ||||||
| chr10:28585348
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+1843C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585348 | ||||||
| chr10:28585602
|
G | A | 288 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.381+2097G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585602 | ||||||
| chr10:28585688
|
G | A | 21 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.381+2183G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585688 | ||||||
| chr10:28585704
|
G | C | 21 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.381+2199G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585704 | ||||||
| chr10:28585908
|
C | T | 1 | a0001c0001t0034g0263 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.381+2403C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585908 | ||||||
| chr10:28585986
|
T | G | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.381+2481T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28585986 | ||||||
| chr10:28586039
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.381+2534A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28586039 | ||||||
| chr10:28586314
|
G | A | 2 | a0001c0001t0040g0227a0001c0001t0040g0228 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.381+2809G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28586314 | ||||||
| chr10:28586466
|
T | C | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.381+2961T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28586466 | ||||||
| chr10:28586714
|
A | T | 1 | a0001c0001t0014g0203 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.382-3022A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28586714 | ||||||
| chr10:28586763
|
T | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.382-2973T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28586763 | ||||||
| chr10:28586797
|
AAAAT | A | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-2938_382-2935d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28586797 | ||||||
| chr10:28587021
|
G | A | 6 | a0001c0001t0012g0277a0001c0001t0018g0278a0001c0001t0018g0283others(3): Show | 6 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-2715G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28587021 | ||||||
| chr10:28587168
|
AATT | A | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.382-2564_382-2562d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 28587168 | |||||
| chr10:28587194
|
A | G | 1 | a0001c0001t0105g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.382-2542A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28587194 | ||||||
| chr10:28587391
|
G | A | 1 | a0001c0001t0082g0147 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.382-2345G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28587391 | ||||||
| chr10:28587758
|
C | G | 1 | a0001c0001t0115g0152 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.382-1978C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28587758 | ||||||
| chr10:28587876
|
G | C | 1 | a0001c0001t0039g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.382-1860G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28587876 | ||||||
| chr10:28587924
|
C | CT | 204 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.382-1802dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 28587924 | |||||
| chr10:28587972
|
T | G | 1 | a0001c0001t0025g0244 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382-1764T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28587972 | ||||||
| chr10:28588007
|
G | C | 2 | a0001c0001t0046g0057a0001c0001t0140g0056 | 2 | NA18994.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.382-1729G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588007 | ||||||
| chr10:28588170
|
G | A | 1 | a0001c0001t0107g0232 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.382-1566G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588170 | ||||||
| chr10:28588236
|
G | A | 1 | a0001c0001t0111g0041 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.382-1500G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588236 | ||||||
| chr10:28588332
|
C | T | 1 | a0001c0001t0003g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382-1404C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588332 | ||||||
| chr10:28588359
|
T | G | 1 | a0001c0001t0101g0075 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.382-1377T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588359 | ||||||
| chr10:28588416
|
A | G | 34 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(31): Show | 34 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.382-1320A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588416 | ||||||
| chr10:28588647
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.382-1089C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588647 | ||||||
| chr10:28588767
|
T | C | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.382-969T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588767 | ||||||
| chr10:28588787
|
C | T | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.382-949C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588787 | ||||||
| chr10:28588830
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.382-906G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588830 | ||||||
| chr10:28588933
|
T | C | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-803T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28588933 | ||||||
| chr10:28589070
|
A | G | 1 | a0001c0001t0120g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.382-666A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28589070 | ||||||
| chr10:28589133
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.382-603A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28589133 | ||||||
| chr10:28589381
|
A | G | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.382-355A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28589381 | ||||||
| chr10:28589450
|
T | C | 1 | a0001c0001t0004g0058 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.382-286T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28589450 | ||||||
| chr10:28589546
|
A | C | 1 | a0001c0001t0129g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.382-190A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 4/13 | chr10 | 28589546 | ||||||
| chr10:28589865
|
A | T | 1 | a0001c0001t0123g0088 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.497+14A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28589865 | ||||||
| chr10:28589920
|
A | G | 2 | a0001c0001t0004g0045a0001c0001t0139g0046 | 2 | HG00733.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.497+69A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28589920 | ||||||
| chr10:28589977
|
G | A | 1 | a0001c0001t0043g0276 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.497+126G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28589977 | ||||||
| chr10:28590028
|
A | G | 4 | a0001c0001t0024g0079a0001c0001t0062g0078a0001c0001t0063g0105others(1): Show | 4 | HG01496.hp1 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+177A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28590028 | ||||||
| chr10:28590088
|
A | G | 1 | a0001c0001t0028g0266 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.497+237A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28590088 | ||||||
| chr10:28590182
|
A | G | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+331A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28590182 | ||||||
| chr10:28590311
|
CA | C | 69 | a0001c0001t0004g0014a0001c0001t0004g0029a0001c0001t0004g0031others(66): Show | 69 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.498-385delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 28590311 | |||||
| chr10:28590311
|
CAA | C | 19 | a0001c0001t0001g0193a0001c0001t0004g0026a0001c0001t0004g0035others(16): Show | 19 | HG01069.hp1 HG01891.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.498-386_498-385del others(2): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 28590311 | |||||
| chr10:28590311
|
CAAA | C | 189 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.498-387_498-385del others(3): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 28590311 | |||||
| chr10:28590311
|
CAAAA | C | 6 | a0001c0001t0001g0171a0001c0001t0001g0217a0001c0001t0005g0172others(3): Show | 6 | HG01192.hp1 HG01261.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-388_498-385del others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 28590311 | |||||
| chr10:28590381
|
A | C | 1 | a0001c0001t0005g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.498-339A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28590381 | ||||||
| chr10:28590549
|
G | A | 2 | a0001c0001t0040g0227a0001c0001t0040g0228 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.498-171G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 5/13 | chr10 | 28590549 | ||||||
| chr10:28590909
|
A | G | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.610+77A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28590909 | ||||||
| chr10:28590944
|
C | T | 1 | a0001c0001t0145g0050 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.610+112C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28590944 | ||||||
| chr10:28591186
|
A | G | 1 | a0001c0001t0018g0278 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.610+354A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591186 | ||||||
| chr10:28591231
|
A | G | 69 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.610+399A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591231 | ||||||
| chr10:28591317
|
TC | T | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.610+486delC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591317 | ||||||
| chr10:28591372
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.610+540A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591372 | ||||||
| chr10:28591375
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.610+543A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591375 | ||||||
| chr10:28591465
|
C | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.610+633C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591465 | ||||||
| chr10:28591833
|
CA | C | 59 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.610+1028delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | |||||
| chr10:28591833
|
CAA | C | 17 | a0001c0001t0003g0083a0001c0001t0028g0285a0001c0001t0062g0078others(14): Show | 17 | HG00735.hp2 HG01069.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.610+1027_610+1028d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | |||||
| chr10:28591833
|
CAAA | C | 43 | a0001c0001t0003g0076a0001c0001t0003g0084a0001c0001t0003g0085others(40): Show | 43 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.610+1026_610+1028d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | |||||
| chr10:28591833
|
CAAAA | C | 26 | a0001c0001t0010g0073a0001c0001t0012g0191a0001c0001t0012g0221others(23): Show | 26 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.610+1025_610+1028d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | |||||
| chr10:28591833
|
CAAAAAAA others(1): Show |
C | 17 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(14): Show | 17 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.610+1021_610+1028d others(10): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | |||||
| chr10:28591833
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0082g0147 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.610+1018_610+1028d others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | |||||
| chr10:28591833
|
CAAAAAAA others(5): Show |
C | 119 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(116): Show | 119 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.610+1017_610+1028d others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | |||||
| chr10:28591833
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0175a0001c0001t0006g0122 | 2 | NA19057.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.610+1016_610+1028d others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28591833 | |||||
| chr10:28591860
|
A | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.610+1028A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28591860 | ||||||
| chr10:28592063
|
T | C | 69 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.610+1231T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592063 | ||||||
| chr10:28592247
|
G | A | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.610+1415G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592247 | ||||||
| chr10:28592328
|
A | G | 8 | a0001c0001t0021g0292a0001c0001t0021g0300a0001c0001t0027g0294others(5): Show | 8 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.610+1496A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592328 | ||||||
| chr10:28592354
|
T | G | 1 | a0001c0001t0039g0252 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.610+1522T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592354 | ||||||
| chr10:28592451
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.610+1619G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592451 | ||||||
| chr10:28592458
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.610+1626C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592458 | ||||||
| chr10:28592475
|
T | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.610+1643T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592475 | ||||||
| chr10:28592535
|
C | T | 1 | a0001c0001t0006g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.610+1703C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592535 | ||||||
| chr10:28592942
|
G | A | 1 | a0001c0001t0142g0016 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.610+2110G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28592942 | ||||||
| chr10:28593082
|
A | G | 1 | a0001c0001t0007g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.610+2250A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593082 | ||||||
| chr10:28593110
|
T | G | 2 | a0001c0001t0043g0289a0001c0001t0117g0288 | 2 | HG00609.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.610+2278T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593110 | ||||||
| chr10:28593152
|
G | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.610+2320G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593152 | ||||||
| chr10:28593596
|
C | T | 1 | a0001c0002t0035g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.611-2137C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593596 | ||||||
| chr10:28593637
|
G | A | 3 | a0002c0003t0026g0068a0002c0003t0026g0229a0002c0003t0041g0230 | 3 | HG02723.hp2 HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.611-2096G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593637 | ||||||
| chr10:28593655
|
C | A | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.611-2078C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593655 | ||||||
| chr10:28593695
|
G | A | 1 | a0001c0001t0062g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.611-2038G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593695 | ||||||
| chr10:28593730
|
C | CA | 14 | a0001c0001t0007g0062a0001c0001t0023g0070a0001c0001t0023g0254others(11): Show | 14 | HG00621.hp1 HG01123.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.611-1990dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28593730 | |||||
| chr10:28593730
|
CA | C | 205 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.611-1990delA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28593730 | |||||
| chr10:28593869
|
A | G | 1 | a0001c0001t0037g0247 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.611-1864A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28593869 | ||||||
| chr10:28594139
|
G | A | 205 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.611-1594G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28594139 | ||||||
| chr10:28594168
|
TTTTG | T | 59 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.611-1561_611-1558d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28594168 | |||||
| chr10:28594298
|
T | C | 3 | a0001c0001t0027g0294a0001c0001t0027g0296a0001c0001t0027g0297 | 3 | HG02965.hp2 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.611-1435T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28594298 | ||||||
| chr10:28594355
|
T | A | 1 | a0001c0001t0107g0232 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.611-1378T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28594355 | ||||||
| chr10:28594408
|
A | G | 1 | a0001c0001t0002g0174 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.611-1325A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28594408 | ||||||
| chr10:28594486
|
T | C | 1 | a0001c0001t0050g0018 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.611-1247T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28594486 | ||||||
| chr10:28595214
|
A | T | 1 | a0001c0001t0123g0088 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.611-519A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595214 | ||||||
| chr10:28595385
|
T | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.611-348T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595385 | ||||||
| chr10:28595396
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.611-337A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595396 | ||||||
| chr10:28595420
|
AT | A | 11 | a0001c0001t0001g0126a0001c0001t0001g0153a0001c0001t0001g0171others(8): Show | 11 | HG00558.hp1 HG01192.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.611-301delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28595420 | |||||
| chr10:28595420
|
ATT | A | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.611-302_611-301del others(2): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 28595420 | |||||
| chr10:28595431
|
T | G | 5 | a0001c0001t0011g0241a0001c0001t0065g0225a0001c0001t0105g0253others(2): Show | 5 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(2): Show |
intron_variant | MODIFIER | c.611-302T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595431 | ||||||
| chr10:28595433
|
G | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.611-300G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595433 | ||||||
| chr10:28595566
|
T | A | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.611-167T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595566 | ||||||
| chr10:28595700
|
C | G | 2 | a0001c0001t0001g0197a0001c0001t0071g0108 | 2 | NA19000.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.611-33C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 6/13 | chr10 | 28595700 | ||||||
| chr10:28596142
|
A | G | 2 | a0001c0001t0011g0249a0001c0001t0025g0244 | 2 | HG01361.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.919+101A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596142 | ||||||
| chr10:28596313
|
G | A | 1 | a0001c0001t0012g0274 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.919+272G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596313 | ||||||
| chr10:28596392
|
TCTTAATA | T | 3 | a0001c0001t0032g0216a0001c0001t0097g0135a0001c0001t0098g0157 | 3 | HG00673.hp2 NA18952.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.919+359_919+365del others(7): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28596392 | |||||
| chr10:28596484
|
G | A | 1 | a0001c0001t0008g0055 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.919+443G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596484 | ||||||
| chr10:28596583
|
T | G | 1 | a0001c0001t0020g0242 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.919+542T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596583 | ||||||
| chr10:28596604
|
T | A | 1 | a0001c0001t0008g0019 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.919+563T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596604 | ||||||
| chr10:28596670
|
A | C | 1 | a0001c0001t0143g0317 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.919+629A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596670 | ||||||
| chr10:28596693
|
A | G | 5 | a0001c0001t0002g0204a0001c0001t0006g0119a0001c0001t0151g0205others(2): Show | 5 | HG00642.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+652A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596693 | ||||||
| chr10:28596745
|
G | A | 1 | a0001c0001t0047g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.919+704G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596745 | ||||||
| chr10:28596746
|
T | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+705T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596746 | ||||||
| chr10:28596859
|
C | G | 3 | a0001c0001t0001g0170a0001c0001t0002g0219a0001c0001t0009g0173 | 3 | HG01243.hp1 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.919+818C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28596859 | ||||||
| chr10:28597056
|
CAT | C | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+1016_919+1017d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597056 | ||||||
| chr10:28597066
|
G | A | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+1025G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597066 | ||||||
| chr10:28597067
|
CATGTAAT others(8): Show |
C | 1 | a0001c0001t0147g0033 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.919+1032_919+1046d others(17): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28597067 | |||||
| chr10:28597118
|
T | G | 3 | a0001c0001t0024g0086a0001c0001t0099g0090a0001c0001t0101g0075 | 3 | HG02523.hp1 NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.919+1077T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597118 | ||||||
| chr10:28597225
|
A | C | 9 | a0001c0001t0002g0168a0001c0001t0002g0204a0001c0001t0006g0119others(6): Show | 9 | HG00642.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+1184A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597225 | ||||||
| chr10:28597409
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+1368A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597409 | ||||||
| chr10:28597518
|
A | G | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.919+1477A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597518 | ||||||
| chr10:28597608
|
A | G | 67 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.919+1567A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597608 | ||||||
| chr10:28597697
|
G | A | 70 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(67): Show | 70 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.919+1656G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597697 | ||||||
| chr10:28597757
|
G | A | 1 | a0001c0002t0013g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.919+1716G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597757 | ||||||
| chr10:28597882
|
G | C | 4 | a0001c0001t0022g0302a0001c0001t0022g0303a0001c0001t0109g0299others(1): Show | 4 | HG01099.hp2 HG02129.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+1841G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28597882 | ||||||
| chr10:28598128
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+2087C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598128 | ||||||
| chr10:28598153
|
T | A | 1 | a0001c0001t0001g0186 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.919+2112T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598153 | ||||||
| chr10:28598158
|
C | T | 2 | a0001c0001t0033g0309a0001c0001t0119g0308 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.919+2117C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598158 | ||||||
| chr10:28598263
|
C | T | 122 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(119): Show | 122 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.919+2222C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598263 | ||||||
| chr10:28598339
|
T | G | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+2298T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598339 | ||||||
| chr10:28598348
|
CTT | C | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+2309_919+2310d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28598348 | |||||
| chr10:28598431
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+2390A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598431 | ||||||
| chr10:28598746
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.919+2705C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598746 | ||||||
| chr10:28598788
|
G | A | 2 | a0001c0001t0014g0215a0001c0001t0017g0214 | 2 | HG00735.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.919+2747G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598788 | ||||||
| chr10:28598991
|
A | T | 1 | a0001c0001t0039g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.919+2950A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28598991 | ||||||
| chr10:28599087
|
AT | A | 60 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(57): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.919+3054delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28599087 | |||||
| chr10:28599133
|
C | T | 1 | a0001c0001t0107g0232 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.919+3092C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599133 | ||||||
| chr10:28599221
|
A | G | 2 | a0001c0001t0012g0265a0001c0001t0028g0266 | 2 | HG00323.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.919+3180A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599221 | ||||||
| chr10:28599510
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.919+3469A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599510 | ||||||
| chr10:28599616
|
G | C | 9 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(6): Show | 9 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+3575G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599616 | ||||||
| chr10:28599672
|
G | A | 3 | a0001c0001t0029g0311a0001c0001t0029g0312a0001c0001t0058g0310 | 3 | HG00639.hp1 HG01175.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.919+3631G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599672 | ||||||
| chr10:28599762
|
T | C | 2 | a0001c0001t0018g0270a0001c0001t0026g0231 | 2 | HG01099.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.919+3721T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599762 | ||||||
| chr10:28599911
|
G | C | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.919+3870G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599911 | ||||||
| chr10:28599960
|
A | C | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.919+3919A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28599960 | ||||||
| chr10:28600227
|
TACTC | T | 121 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(118): Show | 121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.919+4189_919+4192d others(6): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28600227 | |||||
| chr10:28600268
|
AGTC | A | 16 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(13): Show | 16 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+4230_919+4232d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28600268 | |||||
| chr10:28600309
|
A | G | 2 | a0001c0001t0012g0221a0001c0005t0090g0220 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.919+4268A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28600309 | ||||||
| chr10:28600759
|
A | G | 1 | a0001c0001t0120g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.919+4718A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28600759 | ||||||
| chr10:28600945
|
G | A | 4 | a0001c0001t0005g0110a0001c0001t0009g0281a0001c0001t0014g0111others(1): Show | 4 | HG02145.hp1 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+4904G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28600945 | ||||||
| chr10:28600967
|
T | C | 1 | a0001c0001t0143g0317 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.919+4926T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28600967 | ||||||
| chr10:28601119
|
A | G | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.919+5078A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601119 | ||||||
| chr10:28601139
|
T | A | 320 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(317): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.919+5098T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601139 | ||||||
| chr10:28601231
|
C | T | 121 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(118): Show | 121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.919+5190C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601231 | ||||||
| chr10:28601390
|
A | G | 1 | a0001c0001t0043g0276 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.919+5349A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601390 | ||||||
| chr10:28601648
|
C | G | 1 | a0001c0001t0008g0024 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.919+5607C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601648 | ||||||
| chr10:28601680
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+5639C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601680 | ||||||
| chr10:28601755
|
G | T | 3 | a0001c0004t0069g0182a0001c0004t0078g0128a0001c0004t0079g0195 | 3 | HG01069.hp1 HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.919+5714G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601755 | ||||||
| chr10:28601942
|
A | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+5901A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28601942 | ||||||
| chr10:28602046
|
C | T | 1 | a0001c0001t0120g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.919+6005C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28602046 | ||||||
| chr10:28602245
|
A | G | 68 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.920-5941A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28602245 | ||||||
| chr10:28602507
|
A | G | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.920-5679A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28602507 | ||||||
| chr10:28602743
|
G | A | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.920-5443G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28602743 | ||||||
| chr10:28602798
|
G | A | 1 | a0001c0001t0039g0252 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.920-5388G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28602798 | ||||||
| chr10:28603207
|
G | A | 3 | a0001c0001t0061g0268a0001c0001t0093g0178a0001c0001t0094g0167 | 3 | HG02922.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.920-4979G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603207 | ||||||
| chr10:28603255
|
T | C | 1 | a0001c0001t0095g0123 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.920-4931T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603255 | ||||||
| chr10:28603426
|
G | T | 1 | a0001c0001t0003g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.920-4760G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603426 | ||||||
| chr10:28603704
|
A | G | 1 | a0001c0002t0013g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.920-4482A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603704 | ||||||
| chr10:28603826
|
C | T | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.920-4360C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603826 | ||||||
| chr10:28603846
|
A | G | 1 | a0001c0001t0105g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920-4340A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603846 | ||||||
| chr10:28603938
|
AAAAAATA others(39): Show |
A | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.920-4246_920-4201d others(48): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603938 | |||||
| chr10:28603940
|
A | T | 1 | a0001c0001t0025g0244 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.920-4246A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603940 | ||||||
| chr10:28603942
|
A | T | 1 | a0001c0001t0025g0244 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.920-4244A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603942 | ||||||
| chr10:28603942
|
AATATATA others(13): Show |
A | 2 | a0001c0001t0002g0219a0001c0001t0007g0040 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.920-4233_920-4214d others(22): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603942 | |||||
| chr10:28603942
|
AATATATA others(15): Show |
A | 9 | a0001c0001t0001g0146a0001c0001t0002g0151a0001c0001t0005g0282others(6): Show | 9 | HG01069.hp1 HG01123.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-4233_920-4212d others(24): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603942 | |||||
| chr10:28603942
|
AATATATA others(17): Show |
A | 40 | a0001c0001t0001g0126a0001c0001t0001g0130a0001c0001t0001g0158others(37): Show | 40 | HG00639.hp2 HG00673.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.920-4233_920-4210d others(26): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603942 | |||||
| chr10:28603942
|
AATATATA others(19): Show |
A | 1 | a0001c0001t0142g0016 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.920-4233_920-4208d others(28): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603942 | |||||
| chr10:28603942
|
AATATATA others(23): Show |
A | 3 | a0001c0001t0022g0302a0001c0001t0023g0256a0001c0001t0056g0255 | 3 | HG02145.hp2 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.920-4233_920-4204d others(32): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603942 | |||||
| chr10:28603942
|
AATATATA others(25): Show |
A | 12 | a0001c0001t0021g0002a0001c0001t0021g0300a0001c0001t0021g0304others(9): Show | 12 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-4233_920-4202d others(34): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603942 | |||||
| chr10:28603943
|
ATATATAT others(8): Show |
A | 4 | a0001c0001t0024g0079a0001c0001t0024g0086a0001c0001t0101g0075others(1): Show | 4 | HG01934.hp2 HG03927.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-4242_920-4228d others(17): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | ||||||
| chr10:28603943
|
ATATATAT others(10): Show |
A | 2 | a0001c0001t0070g0275a0001c0001t0088g0279 | 2 | HG01168.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.920-4242_920-4226d others(19): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | ||||||
| chr10:28603943
|
ATATATAT others(11): Show |
A | 4 | a0001c0001t0006g0122a0001c0001t0009g0173a0001c0001t0014g0203others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-4233_920-4216d others(20): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603943 | |||||
| chr10:28603943
|
ATATATAT others(12): Show |
A | 17 | a0001c0001t0001g0170a0001c0001t0002g0168a0001c0001t0002g0204others(14): Show | 17 | HG00280.hp2 HG00597.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.920-4242_920-4224d others(21): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | ||||||
| chr10:28603943
|
ATATATAT others(14): Show |
A | 32 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0140others(29): Show | 32 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.920-4242_920-4222d others(23): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | ||||||
| chr10:28603943
|
ATATATAT others(16): Show |
A | 56 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0002g0132others(53): Show | 56 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.920-4242_920-4220d others(25): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | ||||||
| chr10:28603943
|
ATATATAT others(18): Show |
A | 63 | a0001c0001t0001g0153a0001c0001t0004g0026a0001c0001t0004g0029others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.920-4242_920-4218d others(27): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | ||||||
| chr10:28603943
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.920-4242_920-4216d others(29): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | ||||||
| chr10:28603943
|
ATATATAT others(24): Show |
A | 5 | a0001c0001t0021g0292a0001c0001t0023g0070a0001c0001t0023g0254others(2): Show | 5 | HG00099.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-4242_920-4212d others(33): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | ||||||
| chr10:28603943
|
ATATATAT others(26): Show |
A | 1 | a0001c0001t0027g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.920-4242_920-4210d others(35): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | ||||||
| chr10:28603943
|
ATATATAT others(30): Show |
A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-4242_920-4206d others(39): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603943 | ||||||
| chr10:28603944
|
T | A | 31 | a0001c0001t0001g0193a0001c0001t0003g0084a0001c0001t0005g0196others(28): Show | 31 | HG00735.hp1 HG00735.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.920-4242T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603944 | ||||||
| chr10:28603945
|
ATATATAT others(6): Show |
A | 2 | a0001c0001t0010g0081a0001c0001t0100g0320 | 2 | NA18954.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.920-4240_920-4228d others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603945 | ||||||
| chr10:28603945
|
ATATATAT others(9): Show |
A | 5 | a0001c0001t0001g0193a0001c0001t0005g0196a0001c0001t0030g0149others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-4233_920-4218d others(18): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603945 | |||||
| chr10:28603945
|
ATATATAT others(10): Show |
A | 10 | a0001c0001t0003g0084a0001c0001t0006g0284a0001c0001t0010g0080others(7): Show | 10 | HG00735.hp1 HG01975.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.920-4240_920-4224d others(19): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603945 | ||||||
| chr10:28603946
|
T | A | 13 | a0001c0001t0012g0191a0001c0001t0061g0268a0001c0001t0062g0078others(10): Show | 13 | HG00735.hp2 HG01496.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.920-4240T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603946 | ||||||
| chr10:28603947
|
ATATATGT others(4): Show |
A | 2 | a0001c0001t0062g0078a0001c0001t0153g0117 | 2 | HG01496.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.920-4238_920-4228d others(13): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603947 | ||||||
| chr10:28603947
|
ATATATGT others(8): Show |
A | 8 | a0001c0001t0012g0191a0001c0001t0063g0105a0001c0001t0064g0077others(5): Show | 8 | HG00735.hp2 HG01928.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.920-4238_920-4224d others(17): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603947 | ||||||
| chr10:28603948
|
T | A | 3 | a0001c0001t0061g0268a0001c0001t0115g0152a0001c0002t0013g0074 | 3 | HG03098.hp1 NA18906.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.920-4238T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603948 | ||||||
| chr10:28603949
|
ATATGTAT others(6): Show |
A | 1 | a0001c0001t0115g0152 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.920-4236_920-4224d others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603949 | ||||||
| chr10:28603957
|
G | A | 1 | a0001c0001t0024g0099 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.920-4229G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603957 | ||||||
| chr10:28603958
|
T | A | 1 | a0001c0002t0013g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.920-4228T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603958 | ||||||
| chr10:28603960
|
T | A | 7 | a0001c0001t0010g0081a0001c0001t0024g0079a0001c0001t0024g0086others(4): Show | 7 | HG01934.hp2 HG03098.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-4226T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603960 | ||||||
| chr10:28603961
|
G | A | 14 | a0001c0001t0010g0081a0001c0001t0024g0079a0001c0001t0024g0086others(11): Show | 14 | HG01168.hp2 HG01496.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.920-4225G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603961 | ||||||
| chr10:28603961
|
GTA | G | 16 | a0001c0001t0011g0001a0001c0001t0011g0235a0001c0001t0011g0237others(13): Show | 16 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.920-4199_920-4198d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603961 | |||||
| chr10:28603962
|
T | A | 10 | a0001c0001t0001g0193a0001c0001t0005g0196a0001c0001t0006g0122others(7): Show | 10 | HG01243.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.920-4224T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603962 | ||||||
| chr10:28603963
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0025g0233 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.920-4200_920-4199i others(28): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603963 | |||||
| chr10:28603963
|
A | G | 1 | a0002c0003t0041g0223 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.920-4223A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603963 | ||||||
| chr10:28603964
|
T | A | 40 | a0001c0001t0001g0170a0001c0001t0002g0168a0001c0001t0002g0204others(37): Show | 40 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.920-4222T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603964 | ||||||
| chr10:28603965
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0025g0224 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.920-4200_920-4199i others(26): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603965 | |||||
| chr10:28603966
|
T | A | 73 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0140others(70): Show | 73 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.920-4220T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603966 | ||||||
| chr10:28603968
|
T | A | 153 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(150): Show | 153 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.920-4218T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603968 | ||||||
| chr10:28603970
|
T | A | 192 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(189): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.920-4216T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603970 | ||||||
| chr10:28603972
|
T | A | 161 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(158): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.920-4214T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603972 | ||||||
| chr10:28603974
|
T | A | 123 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0170others(120): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.920-4212T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603974 | ||||||
| chr10:28603975
|
ATATATAT others(7): Show |
A | 2 | a0001c0001t0039g0234a0001c0001t0039g0252 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.920-4197_920-4184d others(16): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28603975 | |||||
| chr10:28603976
|
T | A | 88 | a0001c0001t0001g0153a0001c0001t0001g0197a0001c0001t0002g0180others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.920-4210T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603976 | ||||||
| chr10:28603977
|
A | G | 1 | a0002c0003t0041g0223 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.920-4209A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603977 | ||||||
| chr10:28603978
|
T | A | 62 | a0001c0001t0004g0014a0001c0001t0004g0029a0001c0001t0004g0036others(59): Show | 62 | HG00280.hp1 HG00323.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.920-4208T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603978 | ||||||
| chr10:28603978
|
T | C | 2 | a0001c0001t0014g0215a0001c0001t0017g0214 | 2 | HG00735.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.920-4208T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603978 | ||||||
| chr10:28603980
|
T | A | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.920-4206T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603980 | ||||||
| chr10:28603982
|
T | A | 21 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.920-4204T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603982 | ||||||
| chr10:28603984
|
T | A | 17 | a0001c0001t0021g0002a0001c0001t0021g0300a0001c0001t0021g0304others(14): Show | 17 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.920-4202T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603984 | ||||||
| chr10:28603986
|
T | A | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-4200T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603986 | ||||||
| chr10:28603988
|
T | A | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-4198T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603988 | ||||||
| chr10:28603989
|
G | A | 293 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.920-4197G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603989 | ||||||
| chr10:28603991
|
A | G | 2 | a0001c0001t0025g0224a0001c0001t0025g0233 | 2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.920-4195A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28603991 | ||||||
| chr10:28604125
|
T | C | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.920-4061T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604125 | ||||||
| chr10:28604177
|
C | T | 63 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.920-4009C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604177 | ||||||
| chr10:28604182
|
T | G | 7 | a0001c0001t0028g0285a0001c0001t0028g0290a0001c0001t0043g0289others(4): Show | 7 | HG00609.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.920-4004T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604182 | ||||||
| chr10:28604196
|
G | C | 5 | a0001c0001t0007g0023a0001c0001t0007g0030a0001c0001t0007g0042others(2): Show | 5 | NA18948.hp1 NA18964.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-3990G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604196 | ||||||
| chr10:28604198
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.920-3988C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604198 | ||||||
| chr10:28604238
|
G | GT | 14 | a0001c0001t0001g0146a0001c0001t0001g0186a0001c0001t0002g0210others(11): Show | 14 | HG00438.hp1 HG00621.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.920-3934dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28604238 | |||||
| chr10:28604266
|
A | G | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.920-3920A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604266 | ||||||
| chr10:28604368
|
C | T | 1 | a0001c0001t0039g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920-3818C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604368 | ||||||
| chr10:28604442
|
TACA | T | 34 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(31): Show | 34 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.920-3739_920-3737d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28604442 | |||||
| chr10:28604507
|
A | G | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.920-3679A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604507 | ||||||
| chr10:28604562
|
T | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-3624T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604562 | ||||||
| chr10:28604625
|
G | A | 68 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.920-3561G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604625 | ||||||
| chr10:28604685
|
G | A | 224 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(221): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.920-3501G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604685 | ||||||
| chr10:28604790
|
A | C | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.920-3396A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604790 | ||||||
| chr10:28604796
|
T | C | 2 | a0001c0001t0114g0286a0001c0001t0118g0287 | 2 | NA19003.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.920-3390T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604796 | ||||||
| chr10:28604999
|
G | A | 1 | a0001c0002t0013g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.920-3187G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28604999 | ||||||
| chr10:28605139
|
C | T | 1 | a0001c0001t0023g0256 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.920-3047C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605139 | ||||||
| chr10:28605181
|
A | G | 26 | a0001c0001t0012g0191a0001c0001t0012g0265a0001c0001t0012g0274others(23): Show | 26 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.920-3005A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605181 | ||||||
| chr10:28605306
|
A | G | 1 | a0001c0001t0105g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920-2880A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605306 | ||||||
| chr10:28605318
|
C | T | 69 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.920-2868C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605318 | ||||||
| chr10:28605366
|
G | A | 121 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(118): Show | 121 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.920-2820G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605366 | ||||||
| chr10:28605650
|
G | A | 2 | a0001c0001t0021g0300a0001c0001t0042g0298 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.920-2536G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605650 | ||||||
| chr10:28605725
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-2461C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605725 | ||||||
| chr10:28605893
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-2293A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605893 | ||||||
| chr10:28605937
|
G | A | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.920-2249G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28605937 | ||||||
| chr10:28606055
|
GT | G | 283 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.920-2117delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 28606055 | |||||
| chr10:28606058
|
T | G | 2 | a0001c0001t0001g0170a0001c0001t0002g0219 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.920-2128T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606058 | ||||||
| chr10:28606120
|
C | T | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-2066C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606120 | ||||||
| chr10:28606240
|
C | T | 1 | a0001c0001t0075g0148 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.920-1946C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606240 | ||||||
| chr10:28606288
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.920-1898A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606288 | ||||||
| chr10:28606315
|
C | T | 9 | a0001c0001t0004g0058a0001c0001t0008g0011a0001c0001t0008g0055others(6): Show | 9 | HG00280.hp1 HG01109.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-1871C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606315 | ||||||
| chr10:28606316
|
G | A | 1 | a0001c0001t0031g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.920-1870G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606316 | ||||||
| chr10:28606320
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-1866G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606320 | ||||||
| chr10:28606433
|
A | G | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.920-1753A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606433 | ||||||
| chr10:28606437
|
T | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-1749T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606437 | ||||||
| chr10:28606457
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.920-1729C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28606457 | ||||||
| chr10:28607015
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-1171C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28607015 | ||||||
| chr10:28607017
|
G | A | 123 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(120): Show | 123 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.920-1169G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28607017 | ||||||
| chr10:28607121
|
C | T | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.920-1065C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28607121 | ||||||
| chr10:28607488
|
G | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.920-698G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28607488 | ||||||
| chr10:28607699
|
G | T | 1 | a0001c0001t0007g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.920-487G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28607699 | ||||||
| chr10:28608108
|
A | G | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.920-78A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28608108 | ||||||
| chr10:28608121
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.920-65C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28608121 | ||||||
| chr10:28608158
|
T | G | 8 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0219others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.920-28T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 7/13 | chr10 | 28608158 | ||||||
| chr10:28608719
|
G | A | 1 | a0001c0001t0011g0241 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1165+288G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28608719 | ||||||
| chr10:28608756
|
G | A | 203 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1165+325G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28608756 | ||||||
| chr10:28608990
|
G | A | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1165+559G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28608990 | ||||||
| chr10:28609128
|
G | A | 4 | a0001c0001t0023g0070a0001c0001t0023g0254a0001c0001t0023g0256others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165+697G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609128 | ||||||
| chr10:28609133
|
G | A | 1 | a0001c0002t0035g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1165+702G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609133 | ||||||
| chr10:28609168
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1165+737C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609168 | ||||||
| chr10:28609298
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1165+867G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609298 | ||||||
| chr10:28609327
|
C | T | 1 | a0001c0001t0039g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1165+896C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609327 | ||||||
| chr10:28609448
|
T | C | 3 | a0001c0001t0016g0141a0001c0001t0016g0183a0001c0001t0052g0066 | 3 | NA18964.hp2 NA18972.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1165+1017T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609448 | ||||||
| chr10:28609495
|
T | TA | 33 | a0001c0001t0012g0191a0001c0001t0012g0265a0001c0001t0012g0274others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.1165+1065dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 28609495 | |||||
| chr10:28609608
|
G | C | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1166-1091G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609608 | ||||||
| chr10:28609746
|
C | T | 203 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1166-953C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28609746 | ||||||
| chr10:28609926
|
C | CT | 97 | a0001c0001t0002g0144a0001c0001t0003g0076a0001c0001t0003g0083others(94): Show | 97 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1166-752dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 28609926 | |||||
| chr10:28609926
|
C | CTT | 15 | a0001c0001t0003g0101a0001c0001t0007g0040a0001c0001t0012g0221others(12): Show | 15 | HG00609.hp2 HG01243.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1166-753_1166-752d others(4): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 28609926 | |||||
| chr10:28609926
|
C | CTTT | 8 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(5): Show | 8 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1166-754_1166-752d others(5): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 28609926 | |||||
| chr10:28609926
|
CT | C | 21 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0005g0208others(18): Show | 21 | HG00639.hp2 HG01167.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.1166-752delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 28609926 | |||||
| chr10:28610170
|
C | T | 193 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1166-529C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28610170 | ||||||
| chr10:28610277
|
T | C | 2 | a0001c0001t0025g0224a0001c0001t0025g0233 | 2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1166-422T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28610277 | ||||||
| chr10:28610283
|
T | A | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1166-416T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28610283 | ||||||
| chr10:28610306
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1166-393G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28610306 | ||||||
| chr10:28610394
|
T | C | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1166-305T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28610394 | ||||||
| chr10:28610541
|
G | T | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1166-158G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 8/13 | chr10 | 28610541 | ||||||
| chr10:28610855
|
G | T | 1 | a0001c0001t0002g0174 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1288+34G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28610855 | ||||||
| chr10:28610856
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1288+35C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28610856 | ||||||
| chr10:28610889
|
T | C | 2 | a0001c0001t0007g0062a0001c0001t0049g0061 | 2 | HG00621.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1288+68T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28610889 | ||||||
| chr10:28610912
|
A | AT | 193 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1288+102dupT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 28610912 | |||||
| chr10:28610918
|
T | C | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1288+97T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28610918 | ||||||
| chr10:28610984
|
A | G | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1288+163A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28610984 | ||||||
| chr10:28611072
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1288+251G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28611072 | ||||||
| chr10:28611397
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1289-377G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28611397 | ||||||
| chr10:28611727
|
G | T | 1 | a0001c0001t0050g0027 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1289-47G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 9/13 | chr10 | 28611727 | ||||||
| chr10:28612083
|
A | C | 36 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(33): Show | 36 | HG00597.hp1 HG00597.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.1437+161A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28612083 | ||||||
| chr10:28612180
|
A | C | 1 | a0001c0001t0005g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1437+258A>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28612180 | ||||||
| chr10:28612221
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1437+299A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28612221 | ||||||
| chr10:28612379
|
A | G | 1 | a0001c0001t0008g0055 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1437+457A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28612379 | ||||||
| chr10:28612692
|
TC | T | 59 | a0001c0001t0004g0014a0001c0001t0004g0026a0001c0001t0004g0029others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1437+773delC | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 28612692 | |||||
| chr10:28612700
|
G | C | 2 | a0001c0001t0008g0011a0001c0001t0045g0012 | 2 | HG00280.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1437+778G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28612700 | ||||||
| chr10:28613052
|
C | T | 1 | a0001c0001t0011g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1437+1130C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613052 | ||||||
| chr10:28613056
|
A | G | 1 | a0001c0001t0003g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1437+1134A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613056 | ||||||
| chr10:28613142
|
C | T | 1 | a0001c0001t0134g0052 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1437+1220C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613142 | ||||||
| chr10:28613170
|
C | T | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1437+1248C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613170 | ||||||
| chr10:28613194
|
C | T | 1 | a0001c0001t0007g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1437+1272C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613194 | ||||||
| chr10:28613222
|
C | T | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1437+1300C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613222 | ||||||
| chr10:28613253
|
G | T | 1 | a0001c0001t0104g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1438-1314G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613253 | ||||||
| chr10:28613294
|
A | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1438-1273A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613294 | ||||||
| chr10:28613299
|
G | A | 1 | a0001c0001t0005g0282 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1438-1268G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613299 | ||||||
| chr10:28613332
|
C | T | 206 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(203): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1438-1235C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613332 | ||||||
| chr10:28613339
|
C | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1438-1228C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613339 | ||||||
| chr10:28613543
|
T | C | 1 | a0001c0001t0060g0136 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1438-1024T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613543 | ||||||
| chr10:28613689
|
T | G | 123 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(120): Show | 123 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.1438-878T>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613689 | ||||||
| chr10:28613711
|
C | G | 3 | a0001c0001t0001g0170a0001c0001t0002g0219a0001c0001t0009g0173 | 3 | HG01243.hp1 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1438-856C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613711 | ||||||
| chr10:28613924
|
A | G | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1438-643A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28613924 | ||||||
| chr10:28614191
|
C | T | 1 | a0001c0001t0103g0194 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1438-376C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28614191 | ||||||
| chr10:28614233
|
G | A | 1 | a0001c0001t0005g0169 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1438-334G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28614233 | ||||||
| chr10:28614246
|
C | T | 6 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0006g0122others(3): Show | 6 | NA18969.hp1 NA18984.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.1438-321C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28614246 | ||||||
| chr10:28614271
|
A | G | 1 | a0001c0001t0022g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1438-296A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28614271 | ||||||
| chr10:28614307
|
G | GTGTTAGC others(5): Show |
2 | a0001c0001t0006g0156a0001c0001t0102g0280 | 2 | HG00642.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1438-258_1438-257i others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 28614307 | |||||
| chr10:28614345
|
G | A | 4 | a0001c0001t0005g0110a0001c0001t0009g0281a0001c0001t0014g0111others(1): Show | 4 | HG02145.hp1 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1438-222G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28614345 | ||||||
| chr10:28614395
|
A | AGTTTCTT others(6): Show |
1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1438-168_1438-167i others(15): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 28614395 | |||||
| chr10:28614471
|
G | GTCTTCTT others(7): Show |
287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1438-96_1438-95ins others(14): Show |
WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 10/13 | chr10 | 28614471 | ||||||
| chr10:28614735
|
A | G | 1 | a0001c0001t0039g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1556+50A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28614735 | ||||||
| chr10:28614839
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1556+154C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28614839 | ||||||
| chr10:28614842
|
G | A | 206 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(203): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1556+157G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28614842 | ||||||
| chr10:28615000
|
C | G | 6 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0140others(3): Show | 6 | HG01255.hp1 HG01257.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1556+315C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28615000 | ||||||
| chr10:28615158
|
C | T | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1556+473C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28615158 | ||||||
| chr10:28615761
|
C | G | 5 | a0001c0001t0001g0160a0001c0001t0002g0161a0001c0001t0006g0115others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1557-412C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28615761 | ||||||
| chr10:28616150
|
A | G | 69 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.1557-23A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 11/13 | chr10 | 28616150 | ||||||
| chr10:28616520
|
T | C | 5 | a0001c0001t0026g0231a0002c0003t0026g0068a0002c0003t0026g0229others(2): Show | 5 | HG01123.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1746+158T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28616520 | ||||||
| chr10:28616751
|
A | G | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1746+389A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28616751 | ||||||
| chr10:28616824
|
T | A | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1746+462T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28616824 | ||||||
| chr10:28617082
|
C | G | 2 | a0001c0001t0008g0048a0001c0001t0146g0047 | 2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.1747-575C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28617082 | ||||||
| chr10:28617090
|
C | CA | 9 | a0001c0001t0002g0144a0001c0001t0004g0031a0001c0001t0007g0042others(6): Show | 9 | HG00735.hp2 HG01361.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1747-558dupA | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 28617090 | |||||
| chr10:28617105
|
C | G | 1 | a0001c0001t0008g0019 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1747-552C>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28617105 | ||||||
| chr10:28617217
|
T | C | 1 | a0001c0001t0081g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1747-440T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28617217 | ||||||
| chr10:28617252
|
GT | G | 4 | a0001c0001t0024g0079a0001c0001t0062g0078a0001c0001t0063g0105others(1): Show | 4 | HG01496.hp1 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747-402delT | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 28617252 | |||||
| chr10:28617442
|
T | C | 3 | a0001c0001t0012g0221a0001c0001t0012g0222a0001c0005t0090g0220 | 3 | HG01891.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1747-215T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28617442 | ||||||
| chr10:28617518
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1747-139G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 12/13 | chr10 | 28617518 | ||||||
| chr10:28617897
|
A | T | 1 | a0001c0001t0008g0017 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1874+113A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28617897 | ||||||
| chr10:28617960
|
C | T | 1 | a0001c0001t0107g0232 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1874+176C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28617960 | ||||||
| chr10:28618020
|
G | A | 1 | a0001c0001t0014g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1874+236G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28618020 | ||||||
| chr10:28618221
|
T | C | 288 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1874+437T>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28618221 | ||||||
| chr10:28618267
|
A | G | 20 | a0001c0001t0021g0002a0001c0001t0021g0292a0001c0001t0021g0300others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1874+483A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28618267 | ||||||
| chr10:28618366
|
A | AG | 206 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(203): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1874+584dupG | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 28618366 | |||||
| chr10:28618491
|
C | T | 4 | a0001c0001t0024g0079a0001c0001t0062g0078a0001c0001t0063g0105others(1): Show | 4 | HG01496.hp1 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1874+707C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28618491 | ||||||
| chr10:28619066
|
G | A | 1 | a0001c0001t0154g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1875-471G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619066 | ||||||
| chr10:28619069
|
A | G | 3 | a0001c0001t0034g0260a0001c0001t0067g0269a0001c0001t0127g0261 | 3 | HG01256.hp2 HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1875-468A>G | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619069 | ||||||
| chr10:28619104
|
C | T | 2 | a0001c0001t0015g0154a0001c0001t0115g0152 | 2 | HG02135.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1875-433C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619104 | ||||||
| chr10:28619183
|
G | C | 1 | a0001c0001t0017g0120 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1875-354G>C | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619183 | ||||||
| chr10:28619184
|
C | T | 1 | a0001c0001t0017g0120 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1875-353C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619184 | ||||||
| chr10:28619212
|
G | A | 37 | a0001c0001t0001g0126a0001c0001t0001g0158a0001c0001t0001g0175others(34): Show | 37 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1875-325G>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619212 | ||||||
| chr10:28619214
|
A | T | 10 | a0001c0002t0013g0003a0001c0002t0013g0005a0001c0002t0013g0006others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1875-323A>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619214 | ||||||
| chr10:28619245
|
C | A | 287 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1875-292C>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619245 | ||||||
| chr10:28619261
|
C | T | 3 | a0001c0001t0023g0254a0001c0001t0023g0256a0001c0001t0056g0255 | 3 | HG02109.hp1 HG02145.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1875-276C>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619261 | ||||||
| chr10:28619413
|
T | A | 196 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0126others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1875-124T>A | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619413 | ||||||
| chr10:28619510
|
G | T | 6 | a0001c0001t0004g0029a0001c0001t0004g0036a0001c0001t0007g0025others(3): Show | 6 | HG01069.hp2 HG01358.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1875-27G>T | WAC | ENSG00000095787.26 | transcript | ENST00000354911.9 | protein_coding | 13/13 | chr10 | 28619510 |