Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8454 |
|---|---|
| ensemblid | ENSG00000055130.18 |
| hgncid | 2551 |
| symbol | CUL1 |
| name | cullin 1 |
| refseq_nuc | NM_003592.3 |
| refseq_prot | NP_003583.2 |
| ensembl_nuc | ENST00000325222.9 |
| ensembl_prot | ENSP00000326804.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 148698903 |
| end | 148801110 |
| strand | + |
| ver | v1.2 |
| region | chr7:148698903-148801110 |
| region5000 | chr7:148693903-148806110 |
| regionname0 | CUL1_chr7_148698903_148801110 |
| regionname5000 | CUL1_chr7_148693903_148806110 |
| 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 | 776 | 338 | 92 | 70 | 132 | 10 | 32 | 100 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| 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 | 2331 | 318 | 87 | 70 | 117 | 10 | 32 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| c0002 | 0/0 | 2331 | 13 | 0 | 0 | 13 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| c0003 | 0/0 | 2331 | 5 | 5 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| c0004 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| c0005 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 817 | 327 | 83 | 68 | 132 | 10 | 32 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| t0002 | 0/0 | 817 | 9 | 8 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| t0003 | 0/0 | 817 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| t0004 | 0/0 | 817 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| 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 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| 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 | 2331 | 318 | 87 | 70 | 117 | 10 | 32 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| a0001c0002 | 0/0 | 2331 | 13 | 0 | 0 | 13 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| a0001c0003 | 0/0 | 2331 | 5 | 5 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| a0001c0004 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| a0001c0005 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3147 | 307 | 78 | 68 | 117 | 10 | 32 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| a0001c0001t0002 | 0/0 | 3147 | 9 | 8 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| a0001c0001t0003 | 0/0 | 3147 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| a0001c0001t0004 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| a0001c0002t0001 | 0/0 | 3147 | 13 | 0 | 0 | 13 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| a0001c0003t0001 | 0/0 | 3147 | 5 | 5 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| a0001c0004t0001 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| a0001c0005t0001 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | copy fasta | chr7 | 148693903 | 148806110 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0005t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | GBR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0323 | EUR | FIN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00408 | hp1 | a0001 | c0005 | t0001 | g0256 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0123 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | CDX | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02165 | hp1 | a0001 | c0004 | t0001 | g0211 | EAS | CDX | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0264 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0116 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0103 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0102 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | STU | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | STU | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CHB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ASW | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ASW | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | USA | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | USA | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0040 | REF | REF | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0177 | REF | REF | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:148730239
|
G | A | 1 | a0001c0004 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.117G>A | p.Lys39Lys | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/22 | 405/3147 | 117/2331 | 39/776 | chr7 | 148730239 | ||
| chr7:148787021
|
C | T | 1 | a0001c0005 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.1380C>T | p.Asp460Asp | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/22 | 1668/3147 | 1380/2331 | 460/776 | chr7 | 148787021 | ||
| chr7:148792728
|
G | A | 2 | a0001c0002a0001c0005 | 14 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(11): Show |
splice_region_variant&synonymous_variant | LOW | c.1809G>A | p.Ala603Ala | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/22 | 2097/3147 | 1809/2331 | 603/776 | chr7 | 148792728 | ||
| chr7:148799283
|
C | T | 1 | a0001c0003 | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
synonymous_variant | LOW | c.2145C>T | p.Ile715Ile | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/22 | 2433/3147 | 2145/2331 | 715/776 | chr7 | 148799283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:148698983
|
C | T | 1 | a0001c0001t0002 | 9 | HG00735.hp1 HG01884.hp2 HG02723.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-208C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/22 | 31140 | chr7 | 148698983 | |||||
| chr7:148800595
|
G | T | 1 | a0001c0001t0004 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 13 | chr7 | 148800595 | |||||
| chr7:148800671
|
T | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 89 | chr7 | 148800671 | |||||
| chr7:148800683
|
A | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 101 | chr7 | 148800683 | |||||
| chr7:148800684
|
C | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 102 | chr7 | 148800684 | |||||
| chr7:148800685
|
C | A | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 103 | chr7 | 148800685 | |||||
| chr7:148800694
|
A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 112 | chr7 | 148800694 | |||||
| chr7:148800696
|
A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 114 | chr7 | 148800696 | |||||
| chr7:148800697
|
A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 115 | chr7 | 148800697 | |||||
| chr7:148800698
|
A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 116 | chr7 | 148800698 | |||||
| chr7:148800699
|
C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 117 | chr7 | 148800699 | |||||
| chr7:148800701
|
G | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 119 | chr7 | 148800701 | |||||
| chr7:148800702
|
A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*120A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 120 | chr7 | 148800702 | |||||
| chr7:148800705
|
C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*123C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 123 | chr7 | 148800705 | |||||
| chr7:148800706
|
C | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*124C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 124 | chr7 | 148800706 | |||||
| chr7:148800710
|
A | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*128A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 128 | chr7 | 148800710 | |||||
| chr7:148800711
|
C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 129 | chr7 | 148800711 | |||||
| chr7:148800713
|
C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*131C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 131 | chr7 | 148800713 | |||||
| chr7:148800714
|
C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*132C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 132 | chr7 | 148800714 | |||||
| chr7:148800715
|
C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*133C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 133 | chr7 | 148800715 | |||||
| chr7:148800716
|
A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 134 | chr7 | 148800716 | |||||
| chr7:148800718
|
C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*136C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 136 | chr7 | 148800718 | |||||
| chr7:148800719
|
A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 137 | chr7 | 148800719 | |||||
| chr7:148800721
|
C | A | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*139C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 139 | chr7 | 148800721 | |||||
| chr7:148800723
|
G | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*141G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 141 | chr7 | 148800723 | |||||
| chr7:148800726
|
C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*144C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 144 | chr7 | 148800726 | |||||
| chr7:148800731
|
A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 149 | chr7 | 148800731 | |||||
| chr7:148800734
|
T | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 152 | chr7 | 148800734 | |||||
| chr7:148800742
|
A | C | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*160A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 160 | chr7 | 148800742 | |||||
| chr7:148800743
|
A | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*161A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 161 | chr7 | 148800743 | |||||
| chr7:148800749
|
C | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 167 | chr7 | 148800749 | |||||
| chr7:148800750
|
A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 168 | chr7 | 148800750 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:148699061
|
A | T | 81 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-162+32A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699061 | ||||||
| chr7:148699206
|
C | T | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162+177C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699206 | ||||||
| chr7:148699308
|
A | G | 1 | a0001c0001t0001g0335 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-162+279A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699308 | ||||||
| chr7:148699457
|
G | A | 75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-162+428G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699457 | ||||||
| chr7:148699485
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | NA19072.hp1 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-162+456C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699485 | ||||||
| chr7:148699543
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | NA18993.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-162+514C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699543 | ||||||
| chr7:148699563
|
G | A | 88 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-162+534G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699563 | ||||||
| chr7:148699684
|
G | T | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG02257.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-162+655G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699684 | ||||||
| chr7:148699737
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-162+708C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699737 | ||||||
| chr7:148699753
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-162+724C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699753 | ||||||
| chr7:148699807
|
C | G | 1 | a0001c0001t0001g0073 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-162+778C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699807 | ||||||
| chr7:148699957
|
T | C | 5 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(2): Show | 5 | HG02523.hp2 NA18943.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162+928T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699957 | ||||||
| chr7:148699980
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-162+951T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699980 | ||||||
| chr7:148699996
|
G | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG02056.hp1 NA18953.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+967G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699996 | ||||||
| chr7:148700141
|
A | C | 4 | a0001c0001t0001g0333a0001c0002t0001g0331a0001c0002t0001g0332others(1): Show | 4 | NA18957.hp1 NA18960.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162+1112A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148700141 | ||||||
| chr7:148700262
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-162+1233C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148700262 | ||||||
| chr7:148700305
|
C | G | 1 | a0001c0001t0001g0330 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-162+1276C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148700305 | ||||||
| chr7:148700399
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-162+1370A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148700399 | ||||||
| chr7:148700745
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG01978.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-162+1716A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148700745 | ||||||
| chr7:148700799
|
C | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247 | 3 | NA18943.hp1 NA18992.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-162+1770C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148700799 | ||||||
| chr7:148701044
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-162+2015A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701044 | ||||||
| chr7:148701179
|
TAACTTA | T | 75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-162+2158_-162+216 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148701179 | |||||
| chr7:148701208
|
G | C | 227 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 227 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.-162+2179G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701208 | ||||||
| chr7:148701216
|
T | G | 2 | a0001c0002t0001g0255a0001c0005t0001g0256 | 2 | HG00408.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-162+2187T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701216 | ||||||
| chr7:148701242
|
G | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | NA18993.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-162+2213G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701242 | ||||||
| chr7:148701448
|
G | T | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-162+2419G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701448 | ||||||
| chr7:148701541
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162+2512G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701541 | ||||||
| chr7:148701542
|
T | C | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(80): Show | 83 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.-162+2513T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701542 | ||||||
| chr7:148701616
|
G | C | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+2587G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701616 | ||||||
| chr7:148701617
|
A | G | 3 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0329 | 3 | HG02615.hp1 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-162+2588A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701617 | ||||||
| chr7:148701677
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-162+2648C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701677 | ||||||
| chr7:148701866
|
G | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG02257.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-162+2837G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701866 | ||||||
| chr7:148701872
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0134 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-162+2843C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701872 | ||||||
| chr7:148702463
|
C | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+3434C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148702463 | ||||||
| chr7:148703079
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-162+4050C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703079 | ||||||
| chr7:148703226
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-162+4197C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703226 | ||||||
| chr7:148703296
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-162+4267G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703296 | ||||||
| chr7:148703374
|
A | C | 16 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0313others(13): Show | 16 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.-162+4345A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703374 | ||||||
| chr7:148703521
|
T | G | 1 | a0001c0001t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-162+4492T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703521 | ||||||
| chr7:148703521
|
TTTTTTTG | T | 5 | a0001c0001t0001g0091a0001c0001t0001g0239a0001c0001t0001g0242others(2): Show | 5 | HG00738.hp2 HG00741.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162+4513_-162+451 others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148703521 | |||||
| chr7:148703542
|
G | GT | 65 | a0001c0001t0001g0013a0001c0001t0001g0126a0001c0001t0001g0127others(62): Show | 65 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.-162+4521dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148703542 | |||||
| chr7:148703618
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-162+4589C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703618 | ||||||
| chr7:148703669
|
A | G | 6 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 6 | HG00558.hp1 HG02523.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162+4640A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703669 | ||||||
| chr7:148703718
|
G | T | 1 | a0001c0001t0001g0312 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-162+4689G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703718 | ||||||
| chr7:148703914
|
A | T | 1 | a0001c0001t0001g0236 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-162+4885A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703914 | ||||||
| chr7:148703990
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+4961G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703990 | ||||||
| chr7:148704125
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-162+5096A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704125 | ||||||
| chr7:148704156
|
G | GC | 87 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(84): Show | 87 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.-162+5136dupC | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148704156 | |||||
| chr7:148704156
|
G | GCC | 21 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(18): Show | 21 | HG00558.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-162+5135_-162+513 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148704156 | |||||
| chr7:148704158
|
C | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-162+5129C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704158 | ||||||
| chr7:148704159
|
C | G | 3 | a0001c0001t0001g0125a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | HG01952.hp1 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-162+5130C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704159 | ||||||
| chr7:148704316
|
G | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.-162+5287G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704316 | ||||||
| chr7:148704344
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-162+5315A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704344 | ||||||
| chr7:148704563
|
G | A | 6 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162+5534G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704563 | ||||||
| chr7:148704577
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-162+5548G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704577 | ||||||
| chr7:148704811
|
GTTA | G | 31 | a0001c0001t0001g0092a0001c0001t0001g0104a0001c0001t0001g0105others(28): Show | 31 | HG01952.hp1 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.-162+5788_-162+579 others(7): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148704811 | |||||
| chr7:148704841
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-162+5812A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704841 | ||||||
| chr7:148705156
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG03017.hp1 HG03490.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+6127C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148705156 | ||||||
| chr7:148705618
|
T | A | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 92 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.-162+6589T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148705618 | ||||||
| chr7:148705686
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162+6657A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148705686 | ||||||
| chr7:148705736
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-162+6707A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148705736 | ||||||
| chr7:148705892
|
C | G | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 139 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.-162+6863C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148705892 | ||||||
| chr7:148706053
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0258 | 2 | NA18955.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-162+7024G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706053 | ||||||
| chr7:148706077
|
T | C | 16 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(13): Show | 16 | HG01952.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-162+7048T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706077 | ||||||
| chr7:148706102
|
G | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 139 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.-162+7073G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706102 | ||||||
| chr7:148706151
|
A | T | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-162+7122A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706151 | ||||||
| chr7:148706220
|
A | G | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-162+7191A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706220 | ||||||
| chr7:148706346
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162+7317C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706346 | ||||||
| chr7:148706367
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+7338A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706367 | ||||||
| chr7:148706372
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162+7343G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706372 | ||||||
| chr7:148706416
|
A | G | 2 | a0001c0001t0002g0232a0001c0001t0002g0233 | 2 | HG00735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-162+7387A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706416 | ||||||
| chr7:148706600
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-162+7571T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706600 | ||||||
| chr7:148706633
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-162+7604A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706633 | ||||||
| chr7:148706673
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-162+7644G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706673 | ||||||
| chr7:148706825
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(131): Show | 135 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.-162+7796T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706825 | ||||||
| chr7:148707146
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0134 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-162+8117C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707146 | ||||||
| chr7:148707258
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-162+8229G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707258 | ||||||
| chr7:148707287
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 84 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.-162+8258G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707287 | ||||||
| chr7:148707452
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-162+8423A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707452 | ||||||
| chr7:148707585
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-162+8556C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707585 | ||||||
| chr7:148707646
|
A | G | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(2): Show | 5 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162+8617A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707646 | ||||||
| chr7:148707666
|
G | GT | 4 | a0001c0001t0001g0051a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01891.hp1 HG02257.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162+8638dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148707666 | |||||
| chr7:148707790
|
C | T | 6 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162+8761C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707790 | ||||||
| chr7:148707801
|
T | C | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+8772T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707801 | ||||||
| chr7:148707804
|
T | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+8775T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707804 | ||||||
| chr7:148707849
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162+8820C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707849 | ||||||
| chr7:148707850
|
T | G | 54 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0085others(51): Show | 54 | HG00738.hp2 HG00741.hp2 HG01123.hp2 others(51): Show |
intron_variant | MODIFIER | c.-162+8821T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707850 | ||||||
| chr7:148708036
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-162+9007G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148708036 | ||||||
| chr7:148708214
|
C | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG01433.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-162+9185C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148708214 | ||||||
| chr7:148708486
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-162+9457T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148708486 | ||||||
| chr7:148708679
|
T | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162+9650T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148708679 | ||||||
| chr7:148708748
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-162+9719G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148708748 | ||||||
| chr7:148709095
|
T | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG02109.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-162+10066T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709095 | ||||||
| chr7:148709372
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-162+10343G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709372 | ||||||
| chr7:148709377
|
C | G | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162+10348C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709377 | ||||||
| chr7:148709445
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+10416G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709445 | ||||||
| chr7:148709455
|
C | T | 2 | a0001c0003t0001g0102a0001c0003t0001g0103 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-162+10426C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709455 | ||||||
| chr7:148709582
|
A | C | 15 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 15 | HG01952.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-162+10553A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709582 | ||||||
| chr7:148709615
|
A | G | 2 | a0001c0001t0001g0305a0001c0001t0001g0306 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-162+10586A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709615 | ||||||
| chr7:148709703
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-162+10674G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709703 | ||||||
| chr7:148709767
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-162+10738A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709767 | ||||||
| chr7:148709885
|
C | T | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+10856C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709885 | ||||||
| chr7:148710143
|
C | A | 15 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 15 | HG01952.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-162+11114C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710143 | ||||||
| chr7:148710305
|
T | TGGCTC | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 139 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.-162+11276_-162+11 others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710305 | ||||||
| chr7:148710307
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-162+11278C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710307 | ||||||
| chr7:148710357
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-162+11328G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710357 | ||||||
| chr7:148710368
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | NA19064.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-162+11339G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710368 | ||||||
| chr7:148710369
|
A | G | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG02109.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-162+11340A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710369 | ||||||
| chr7:148710390
|
A | G | 7 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 7 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-162+11361A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710390 | ||||||
| chr7:148710433
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+11404G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710433 | ||||||
| chr7:148710493
|
C | T | 9 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0298others(6): Show | 9 | HG00408.hp2 HG00642.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+11464C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710493 | ||||||
| chr7:148710721
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+11692C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710721 | ||||||
| chr7:148710807
|
G | C | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-162+11778G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710807 | ||||||
| chr7:148710824
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0228a0001c0001t0001g0229 | 4 | HG01099.hp2 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162+11795C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710824 | ||||||
| chr7:148710831
|
T | A | 14 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(11): Show | 14 | HG01952.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-162+11802T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710831 | ||||||
| chr7:148710921
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-162+11892G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710921 | ||||||
| chr7:148711056
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-162+12027C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711056 | ||||||
| chr7:148711186
|
A | G | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 95 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.-162+12157A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711186 | ||||||
| chr7:148711227
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-162+12198C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711227 | ||||||
| chr7:148711228
|
G | C | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-162+12199G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711228 | ||||||
| chr7:148711230
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-162+12201A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711230 | ||||||
| chr7:148711285
|
C | T | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+12256C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711285 | ||||||
| chr7:148711489
|
G | A | 5 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(2): Show | 5 | HG01070.hp1 HG01081.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+12460G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711489 | ||||||
| chr7:148711562
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | NA19072.hp1 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-162+12533G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711562 | ||||||
| chr7:148711594
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+12565G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711594 | ||||||
| chr7:148711653
|
CAG | C | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+12625_-162+12 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711653 | ||||||
| chr7:148711667
|
C | G | 2 | a0001c0001t0001g0297a0001c0001t0001g0310 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-162+12638C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711667 | ||||||
| chr7:148711685
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-162+12656A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711685 | ||||||
| chr7:148711927
|
C | T | 6 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(3): Show | 6 | HG01928.hp1 HG01934.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162+12898C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711927 | ||||||
| chr7:148711991
|
T | A | 1 | a0001c0001t0001g0308 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-162+12962T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711991 | ||||||
| chr7:148712075
|
C | A | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | NA18941.hp1 NA18948.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+13046C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712075 | ||||||
| chr7:148712304
|
A | G | 15 | a0001c0001t0001g0092a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-162+13275A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712304 | ||||||
| chr7:148712475
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162+13446A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712475 | ||||||
| chr7:148712716
|
A | C | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-162+13687A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712716 | ||||||
| chr7:148712776
|
C | T | 2 | a0001c0001t0001g0303a0001c0001t0001g0304 | 2 | HG00408.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-162+13747C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712776 | ||||||
| chr7:148712849
|
A | G | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 110 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.-162+13820A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712849 | ||||||
| chr7:148712854
|
T | A | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-162+13825T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712854 | ||||||
| chr7:148712990
|
G | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162+13961G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712990 | ||||||
| chr7:148713001
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-162+13972T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713001 | ||||||
| chr7:148713031
|
A | C | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 95 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.-162+14002A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713031 | ||||||
| chr7:148713300
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-162+14271T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713300 | ||||||
| chr7:148713302
|
G | A | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+14273G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713302 | ||||||
| chr7:148713318
|
T | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+14289T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713318 | ||||||
| chr7:148713378
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-162+14349G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713378 | ||||||
| chr7:148713619
|
G | A | 28 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0094others(25): Show | 28 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-162+14590G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713619 | ||||||
| chr7:148713735
|
A | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0268 | 2 | HG02257.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-162+14706A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713735 | ||||||
| chr7:148713736
|
T | TTTTTTGA others(6): Show |
1 | a0001c0002t0001g0334 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-162+14708_-162+14 others(19): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148713736 | |||||
| chr7:148713737
|
T | A | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-162+14708T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713737 | ||||||
| chr7:148713754
|
C | CA | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+14726dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148713754 | |||||
| chr7:148713907
|
A | G | 9 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(6): Show | 9 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-162+14878A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713907 | ||||||
| chr7:148713966
|
T | C | 138 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 138 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.-162+14937T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713966 | ||||||
| chr7:148713999
|
C | T | 6 | a0001c0001t0001g0091a0001c0001t0001g0237a0001c0001t0001g0239others(3): Show | 6 | HG00738.hp2 HG00741.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162+14970C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713999 | ||||||
| chr7:148714549
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-161-15413T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714549 | ||||||
| chr7:148714622
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-161-15340C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714622 | ||||||
| chr7:148714696
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-15266T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714696 | ||||||
| chr7:148714711
|
G | A | 12 | a0001c0001t0001g0091a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-161-15251G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714711 | ||||||
| chr7:148714717
|
A | AT | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 89 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-161-15241dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148714717 | |||||
| chr7:148714730
|
G | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 89 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-161-15232G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714730 | ||||||
| chr7:148714768
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-161-15194C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714768 | ||||||
| chr7:148714793
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-161-15169G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714793 | ||||||
| chr7:148714887
|
G | C | 6 | a0001c0001t0001g0091a0001c0001t0001g0237a0001c0001t0001g0239others(3): Show | 6 | HG00738.hp2 HG00741.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-15075G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714887 | ||||||
| chr7:148715011
|
A | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0122 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-161-14951A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715011 | ||||||
| chr7:148715279
|
A | G | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(92): Show | 95 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.-161-14683A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715279 | ||||||
| chr7:148715310
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-161-14652G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715310 | ||||||
| chr7:148715360
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-161-14602G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715360 | ||||||
| chr7:148715398
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-161-14564C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715398 | ||||||
| chr7:148715418
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-161-14544T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715418 | ||||||
| chr7:148715421
|
A | G | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 139 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.-161-14541A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715421 | ||||||
| chr7:148715429
|
C | T | 6 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-14533C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715429 | ||||||
| chr7:148715526
|
T | C | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 89 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-161-14436T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715526 | ||||||
| chr7:148715612
|
A | C | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-161-14350A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715612 | ||||||
| chr7:148715789
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-14173T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715789 | ||||||
| chr7:148716136
|
T | TTC | 6 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(3): Show | 6 | HG01928.hp1 HG01934.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-13824_-161-13 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148716136 | |||||
| chr7:148716191
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-13771A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716191 | ||||||
| chr7:148716340
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-161-13622C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716340 | ||||||
| chr7:148716508
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-161-13454C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716508 | ||||||
| chr7:148716709
|
G | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 139 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.-161-13253G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716709 | ||||||
| chr7:148716725
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-161-13237C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716725 | ||||||
| chr7:148716885
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-161-13077G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716885 | ||||||
| chr7:148716961
|
G | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-13001G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716961 | ||||||
| chr7:148716967
|
A | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0051 | 2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-161-12995A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716967 | ||||||
| chr7:148716977
|
A | G | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG00597.hp2 NA18966.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-161-12985A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716977 | ||||||
| chr7:148717043
|
T | TTTTTG | 15 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0027others(12): Show | 15 | HG01952.hp1 HG02615.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-161-12888_-161-12 others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148717043 | |||||
| chr7:148717043
|
T | TTTTTGTT others(3): Show |
65 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 65 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-161-12893_-161-12 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148717043 | |||||
| chr7:148717043
|
T | TTTTTGTT others(8): Show |
1 | a0001c0001t0001g0019 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-161-12898_-161-12 others(21): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148717043 | |||||
| chr7:148717043
|
TTTTTGTT others(3): Show |
T | 1 | a0001c0001t0001g0308 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-161-12893_-161-12 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148717043 | |||||
| chr7:148717088
|
C | A | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | NA18941.hp1 NA18948.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-12874C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717088 | ||||||
| chr7:148717365
|
G | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG02155.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-161-12597G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717365 | ||||||
| chr7:148717418
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-12544A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717418 | ||||||
| chr7:148717451
|
C | A | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-161-12511C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717451 | ||||||
| chr7:148717489
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-161-12473A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717489 | ||||||
| chr7:148717704
|
A | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-12258A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717704 | ||||||
| chr7:148717805
|
A | T | 4 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | NA18975.hp1 NA19007.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.-161-12157A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717805 | ||||||
| chr7:148717828
|
T | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | NA19072.hp1 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-161-12134T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717828 | ||||||
| chr7:148717863
|
G | A | 26 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(23): Show | 26 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.-161-12099G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717863 | ||||||
| chr7:148717957
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-161-12005C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717957 | ||||||
| chr7:148718321
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-161-11641A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148718321 | ||||||
| chr7:148718477
|
T | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-161-11485T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148718477 | ||||||
| chr7:148718554
|
A | AT | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.-161-11398dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148718554 | |||||
| chr7:148718648
|
T | C | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 115 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.-161-11314T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148718648 | ||||||
| chr7:148718718
|
AT | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.-161-11236delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148718718 | |||||
| chr7:148718819
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-161-11143A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148718819 | ||||||
| chr7:148719012
|
G | T | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 144 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.-161-10950G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719012 | ||||||
| chr7:148719316
|
A | AT | 15 | a0001c0001t0001g0092a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-161-10646_-161-10 others(7): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719316 | ||||||
| chr7:148719316
|
A | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0244 | 2 | HG00738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-161-10646A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719316 | ||||||
| chr7:148719642
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-161-10320A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719642 | ||||||
| chr7:148719745
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-161-10217C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719745 | ||||||
| chr7:148719746
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-161-10216G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719746 | ||||||
| chr7:148719764
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-161-10198T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719764 | ||||||
| chr7:148719840
|
C | G | 1 | a0001c0001t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-161-10122C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719840 | ||||||
| chr7:148719981
|
C | T | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 144 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.-161-9981C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719981 | ||||||
| chr7:148720059
|
A | G | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-161-9903A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720059 | ||||||
| chr7:148720071
|
A | G | 15 | a0001c0001t0001g0092a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-161-9891A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720071 | ||||||
| chr7:148720245
|
T | C | 9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-161-9717T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720245 | ||||||
| chr7:148720252
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-161-9710C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720252 | ||||||
| chr7:148720598
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-161-9364A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720598 | ||||||
| chr7:148720662
|
A | G | 1 | a0001c0001t0002g0213 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-161-9300A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720662 | ||||||
| chr7:148720820
|
A | T | 1 | a0001c0001t0001g0212 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-161-9142A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720820 | ||||||
| chr7:148721034
|
T | C | 15 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 15 | HG01952.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-161-8928T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721034 | ||||||
| chr7:148721048
|
G | A | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 144 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.-161-8914G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721048 | ||||||
| chr7:148721089
|
T | G | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 111 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.-161-8873T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721089 | ||||||
| chr7:148721365
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-161-8597C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721365 | ||||||
| chr7:148721438
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-161-8524T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721438 | ||||||
| chr7:148721463
|
T | C | 9 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(6): Show | 9 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-161-8499T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721463 | ||||||
| chr7:148721511
|
C | T | 1 | a0001c0004t0001g0211 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-161-8451C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721511 | ||||||
| chr7:148721518
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-8444A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721518 | ||||||
| chr7:148721705
|
G | C | 1 | a0001c0001t0001g0148 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-161-8257G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721705 | ||||||
| chr7:148721709
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-8253A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721709 | ||||||
| chr7:148721724
|
C | CT | 11 | a0001c0001t0001g0092a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-161-8229dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148721724 | |||||
| chr7:148721739
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-8223A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721739 | ||||||
| chr7:148721793
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 43 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-161-8169G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721793 | ||||||
| chr7:148721818
|
A | G | 6 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0073others(3): Show | 6 | NA18966.hp1 NA18998.hp1 NA19072.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-8144A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721818 | ||||||
| chr7:148721974
|
C | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 43 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-161-7988C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721974 | ||||||
| chr7:148722068
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121 | 3 | HG02055.hp1 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-161-7894T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722068 | ||||||
| chr7:148722283
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-161-7679C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722283 | ||||||
| chr7:148722379
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-161-7583G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722379 | ||||||
| chr7:148722392
|
A | C | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(54): Show | 57 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-161-7570A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722392 | ||||||
| chr7:148722487
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-7475C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722487 | ||||||
| chr7:148722502
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-161-7460G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722502 | ||||||
| chr7:148722687
|
T | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0101 | 3 | HG01123.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-161-7275T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722687 | ||||||
| chr7:148722688
|
T | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0101 | 3 | HG01123.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-161-7274T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722688 | ||||||
| chr7:148722690
|
C | T | 32 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0094others(29): Show | 32 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-161-7272C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722690 | ||||||
| chr7:148722955
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0134 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-161-7007A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722955 | ||||||
| chr7:148723017
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-6945G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723017 | ||||||
| chr7:148723082
|
GT | G | 9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-161-6878delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148723082 | |||||
| chr7:148723322
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-6640C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723322 | ||||||
| chr7:148723417
|
A | G | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.-161-6545A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723417 | ||||||
| chr7:148723653
|
A | G | 11 | a0001c0001t0001g0092a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-161-6309A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723653 | ||||||
| chr7:148723662
|
CA | C | 42 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(39): Show | 42 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.-161-6288delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148723662 | |||||
| chr7:148723662
|
CAA | C | 102 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 102 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.-161-6289_-161-628 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148723662 | |||||
| chr7:148723743
|
C | T | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-161-6219C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723743 | ||||||
| chr7:148723774
|
G | C | 1 | a0001c0001t0001g0298 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-161-6188G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723774 | ||||||
| chr7:148723789
|
C | CT | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 43 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-161-6160dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148723789 | |||||
| chr7:148723789
|
C | CTT | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 56 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-161-6161_-161-616 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148723789 | |||||
| chr7:148723801
|
T | C | 11 | a0001c0001t0001g0092a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-161-6161T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723801 | ||||||
| chr7:148723997
|
T | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0134 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-161-5965T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723997 | ||||||
| chr7:148724049
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | HG02970.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-161-5913A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724049 | ||||||
| chr7:148724100
|
C | T | 9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-161-5862C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724100 | ||||||
| chr7:148724436
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0066 | 3 | NA19067.hp2 NA19075.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-161-5526C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724436 | ||||||
| chr7:148724479
|
T | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.-161-5483T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724479 | ||||||
| chr7:148724481
|
C | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-5481C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724481 | ||||||
| chr7:148724521
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-5441C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724521 | ||||||
| chr7:148724527
|
G | A | 5 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0116others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-5435G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724527 | ||||||
| chr7:148724601
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0134 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-161-5361T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724601 | ||||||
| chr7:148724841
|
TTTTTTTG others(4): Show |
T | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-161-5104_-161-509 others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148724841 | |||||
| chr7:148724904
|
A | T | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-161-5058A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724904 | ||||||
| chr7:148725024
|
A | G | 12 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(9): Show | 12 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-161-4938A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725024 | ||||||
| chr7:148725182
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-161-4780C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725182 | ||||||
| chr7:148725198
|
T | TACACACA others(5): Show |
1 | a0001c0001t0001g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-161-4761_-161-475 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725198 | |||||
| chr7:148725198
|
TAC | T | 17 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0091others(14): Show | 17 | HG00423.hp2 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-161-4751_-161-475 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725198 | |||||
| chr7:148725202
|
C | CACGCAGC others(6): Show |
1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-161-4758_-161-475 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725202 | |||||
| chr7:148725202
|
C | CACGCGCG others(5): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0066 | 2 | NA19067.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-161-4758_-161-475 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725202 | |||||
| chr7:148725207
|
A | ACG | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | NA18943.hp2 NA18961.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-161-4754_-161-475 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725207 | |||||
| chr7:148725207
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0070 | 2 | HG03834.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-161-4755A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725207 | ||||||
| chr7:148725209
|
A | ACG | 6 | a0001c0001t0001g0205a0001c0001t0001g0291a0001c0001t0001g0316others(3): Show | 6 | HG01081.hp2 HG01109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-4752_-161-475 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725209 | |||||
| chr7:148725209
|
A | G | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 85 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.-161-4753A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725209 | ||||||
| chr7:148725211
|
A | G | 168 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(165): Show | 168 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.-161-4751A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725211 | ||||||
| chr7:148725211
|
ACGCGCG | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0251others(2): Show | 5 | HG02258.hp1 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4747_-161-474 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725211 | |||||
| chr7:148725211
|
ACGCGCGC others(3): Show |
A | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-161-4749_-161-474 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725211 | |||||
| chr7:148725213
|
G | A | 6 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0092others(3): Show | 6 | HG01978.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-4749G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725213 | ||||||
| chr7:148725214
|
C | CGT | 14 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(11): Show | 14 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-161-4747_-161-474 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725214 | |||||
| chr7:148725215
|
G | A | 6 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0092others(3): Show | 6 | HG01978.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-4747G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725215 | ||||||
| chr7:148725216
|
C | T | 18 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0104others(15): Show | 18 | HG01952.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-161-4746C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725216 | ||||||
| chr7:148725217
|
G | A | 7 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0092others(4): Show | 7 | HG01978.hp2 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-161-4745G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725217 | ||||||
| chr7:148725217
|
G | GCACACAC others(7): Show |
3 | a0001c0003t0001g0116a0001c0003t0001g0123a0001c0003t0001g0264 | 3 | HG02145.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-161-4744_-161-474 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725217 | |||||
| chr7:148725217
|
G | GCACGCGC others(17): Show |
1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-161-4744_-161-474 others(28): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725217 | |||||
| chr7:148725219
|
G | A | 18 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0072others(15): Show | 18 | HG01978.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-161-4743G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725219 | ||||||
| chr7:148725219
|
G | GCA | 5 | a0001c0001t0001g0273a0001c0002t0001g0203a0001c0002t0001g0331others(2): Show | 5 | NA18957.hp1 NA18960.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCACACAC others(1): Show |
3 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0053 | 3 | HG03490.hp2 HG03492.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCACACAC others(5): Show |
2 | a0001c0001t0001g0019a0001c0001t0001g0149 | 2 | HG03710.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCA | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0063others(2): Show | 5 | HG02155.hp1 HG02523.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCACA | 5 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0079others(2): Show | 5 | HG00558.hp2 HG02109.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCACAC others(1): Show |
6 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0060others(3): Show | 6 | HG03017.hp1 HG03491.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCACAC others(3): Show |
8 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG01081.hp1 HG01192.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCACAC others(5): Show |
15 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0026others(12): Show | 15 | HG00621.hp1 HG01884.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCACAC others(7): Show |
8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(5): Show | 8 | HG00438.hp2 HG00741.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCACAC others(9): Show |
1 | a0001c0001t0001g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCACAC others(15): Show |
1 | a0001c0001t0001g0025 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(26): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCACAC others(31): Show |
1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(42): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCACAC others(35): Show |
1 | a0001c0001t0001g0034 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(46): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCACGC others(17): Show |
1 | a0001c0001t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(28): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCACGC others(21): Show |
1 | a0001c0001t0001g0013 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(32): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCACGC others(25): Show |
1 | a0001c0001t0001g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(36): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCAC others(3): Show |
1 | a0001c0001t0001g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCAC others(5): Show |
6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(3): Show | 6 | HG01358.hp2 HG01891.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCAC others(7): Show |
2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCAC others(9): Show |
5 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG00639.hp2 HG00738.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCAC others(11): Show |
1 | a0001c0001t0001g0064 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(22): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCAC others(13): Show |
1 | a0001c0001t0001g0042 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(24): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCAC others(15): Show |
1 | a0001c0001t0001g0017 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(26): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCAC others(23): Show |
1 | a0001c0001t0001g0016 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(34): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCAC others(33): Show |
1 | a0001c0001t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(44): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCAC others(39): Show |
1 | a0001c0001t0001g0011 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(50): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCGC others(7): Show |
1 | a0001c0001t0001g0008 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCGC others(9): Show |
1 | a0001c0001t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCGC others(15): Show |
1 | a0001c0003t0001g0103 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(26): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCGC others(27): Show |
1 | a0001c0003t0001g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(38): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCGC others(9): Show |
1 | a0001c0001t0001g0066 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCGC others(15): Show |
1 | a0001c0001t0001g0242 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(26): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCGC others(11): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0239 | 2 | HG00738.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(22): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
G | GCGCGCGC others(13): Show |
1 | a0001c0001t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(24): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725219
|
GCTCA | G | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(2): Show | 5 | HG01952.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4741_-161-473 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | |||||
| chr7:148725221
|
T | A | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(170): Show | 173 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.-161-4741T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725221 | ||||||
| chr7:148725221
|
T | G | 45 | a0001c0001t0001g0029a0001c0001t0001g0068a0001c0001t0001g0073others(42): Show | 45 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-161-4741T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725221 | ||||||
| chr7:148725221
|
T | TCA | 6 | a0001c0001t0001g0161a0001c0001t0001g0215a0001c0001t0001g0230others(3): Show | 6 | HG01346.hp2 HG01433.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-4715_-161-471 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725221 | |||||
| chr7:148725223
|
A | G | 20 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0119others(17): Show | 20 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.-161-4739A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725223 | ||||||
| chr7:148725225
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(3): Show | 6 | HG01175.hp2 HG01952.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-4737A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725225 | ||||||
| chr7:148725227
|
A | G | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(2): Show | 5 | HG01952.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4735A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725227 | ||||||
| chr7:148725231
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-161-4731A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725231 | ||||||
| chr7:148725247
|
A | C | 10 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(7): Show | 10 | HG00741.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-161-4715A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725247 | ||||||
| chr7:148725248
|
C | CA | 3 | a0001c0001t0001g0303a0001c0001t0001g0323a0001c0001t0002g0162 | 3 | HG00280.hp2 NA18998.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-161-4714_-161-471 others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725248 | ||||||
| chr7:148725248
|
C | CACACACA others(4): Show |
1 | a0001c0001t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-161-4714_-161-471 others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725248 | ||||||
| chr7:148725248
|
C | CACACACA others(6): Show |
1 | a0001c0001t0001g0073 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-161-4714_-161-471 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725248 | ||||||
| chr7:148725249
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-161-4713C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725249 | ||||||
| chr7:148725260
|
T | C | 5 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0116others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-4702T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725260 | ||||||
| chr7:148725274
|
T | G | 1 | a0001c0001t0001g0037 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-161-4688T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725274 | ||||||
| chr7:148725286
|
C | T | 11 | a0001c0001t0001g0092a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-161-4676C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725286 | ||||||
| chr7:148725408
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-4554C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725408 | ||||||
| chr7:148725489
|
A | G | 5 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0242others(2): Show | 5 | HG00738.hp2 HG00741.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-4473A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725489 | ||||||
| chr7:148725491
|
A | T | 1 | a0001c0001t0001g0296 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-161-4471A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725491 | ||||||
| chr7:148725591
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-161-4371C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725591 | ||||||
| chr7:148725815
|
T | C | 1 | a0001c0001t0001g0325 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-161-4147T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725815 | ||||||
| chr7:148726254
|
T | C | 6 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-3708T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726254 | ||||||
| chr7:148726301
|
G | A | 6 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-3661G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726301 | ||||||
| chr7:148726400
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-161-3562A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726400 | ||||||
| chr7:148726468
|
C | T | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(95): Show | 98 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.-161-3494C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726468 | ||||||
| chr7:148726532
|
G | A | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.-161-3430G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726532 | ||||||
| chr7:148726621
|
A | G | 5 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0116others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-3341A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726621 | ||||||
| chr7:148726747
|
G | C | 1 | a0001c0001t0001g0003 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-161-3215G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726747 | ||||||
| chr7:148726825
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-161-3137A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726825 | ||||||
| chr7:148726833
|
C | CA | 28 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0028others(25): Show | 28 | HG00280.hp2 HG01070.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-161-3112dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148726833 | |||||
| chr7:148726833
|
C | CAA | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-161-3113_-161-311 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148726833 | |||||
| chr7:148726850
|
AT | A | 11 | a0001c0001t0001g0083a0001c0001t0001g0117a0001c0001t0001g0118others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-161-3103delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148726850 | |||||
| chr7:148726851
|
T | A | 109 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 109 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.-161-3111T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726851 | ||||||
| chr7:148726852
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-3110T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726852 | ||||||
| chr7:148727090
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-161-2872G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727090 | ||||||
| chr7:148727151
|
A | G | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.-161-2811A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727151 | ||||||
| chr7:148727155
|
A | G | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.-161-2807A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727155 | ||||||
| chr7:148727385
|
T | C | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-161-2577T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727385 | ||||||
| chr7:148727449
|
T | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0163 | 3 | HG02155.hp2 HG03942.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-161-2513T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727449 | ||||||
| chr7:148727527
|
C | T | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG00642.hp2 HG01192.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-2435C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727527 | ||||||
| chr7:148727930
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-161-2032A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727930 | ||||||
| chr7:148727936
|
A | G | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 94 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.-161-2026A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727936 | ||||||
| chr7:148727953
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-161-2009C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727953 | ||||||
| chr7:148728050
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-1912C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728050 | ||||||
| chr7:148728212
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-161-1750C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728212 | ||||||
| chr7:148728250
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-161-1712G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728250 | ||||||
| chr7:148728323
|
A | G | 17 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0092others(14): Show | 17 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-161-1639A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728323 | ||||||
| chr7:148728710
|
A | C | 1 | a0001c0001t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-161-1252A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728710 | ||||||
| chr7:148728823
|
T | A | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.-161-1139T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728823 | ||||||
| chr7:148728860
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0034others(1): Show | 4 | HG02165.hp2 NA18971.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-161-1102A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728860 | ||||||
| chr7:148728876
|
G | C | 1 | a0001c0001t0004g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-161-1086G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728876 | ||||||
| chr7:148729179
|
T | G | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.-161-783T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729179 | ||||||
| chr7:148729224
|
T | C | 1 | a0001c0001t0001g0307 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-161-738T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729224 | ||||||
| chr7:148729382
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-161-580C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729382 | ||||||
| chr7:148729580
|
A | C | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 114 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-161-382A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729580 | ||||||
| chr7:148729594
|
T | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02615.hp2 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-161-368T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729594 | ||||||
| chr7:148729625
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-161-337T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729625 | ||||||
| chr7:148729628
|
C | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-161-334C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729628 | ||||||
| chr7:148729752
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-210C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729752 | ||||||
| chr7:148730342
|
A | G | 11 | a0001c0001t0001g0092a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+80A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730342 | ||||||
| chr7:148730378
|
A | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG00642.hp1 HG01123.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.140+116A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730378 | ||||||
| chr7:148730381
|
G | T | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG00597.hp2 NA18966.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.140+119G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730381 | ||||||
| chr7:148730414
|
A | G | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+152A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730414 | ||||||
| chr7:148730498
|
A | T | 32 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0094others(29): Show | 32 | HG00738.hp2 HG00741.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.140+236A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730498 | ||||||
| chr7:148730601
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140+339T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730601 | ||||||
| chr7:148730644
|
A | G | 9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+382A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730644 | ||||||
| chr7:148730699
|
A | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140+437A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730699 | ||||||
| chr7:148730781
|
G | A | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.140+519G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730781 | ||||||
| chr7:148730889
|
G | T | 9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+627G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730889 | ||||||
| chr7:148730900
|
T | C | 6 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+638T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730900 | ||||||
| chr7:148731091
|
C | T | 6 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+829C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731091 | ||||||
| chr7:148731196
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140+934C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731196 | ||||||
| chr7:148731393
|
A | G | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG02647.hp1 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.140+1131A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731393 | ||||||
| chr7:148731431
|
C | T | 5 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0116others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+1169C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731431 | ||||||
| chr7:148731657
|
G | A | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+1395G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731657 | ||||||
| chr7:148731658
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+1396A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731658 | ||||||
| chr7:148731801
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.140+1539G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731801 | ||||||
| chr7:148731844
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0122 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.140+1582G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731844 | ||||||
| chr7:148731859
|
C | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0146a0001c0001t0001g0191others(7): Show | 11 | HG01928.hp2 HG01934.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.140+1597C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731859 | ||||||
| chr7:148732022
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.140+1760G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732022 | ||||||
| chr7:148732108
|
T | C | 3 | a0001c0003t0001g0116a0001c0003t0001g0123a0001c0003t0001g0264 | 3 | HG02145.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.140+1846T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732108 | ||||||
| chr7:148732261
|
G | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140+1999G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732261 | ||||||
| chr7:148732320
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.140+2058A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732320 | ||||||
| chr7:148732345
|
A | AT | 18 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0064others(15): Show | 18 | HG00438.hp1 HG00738.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+2101dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148732345 | |||||
| chr7:148732345
|
AT | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | HG01433.hp2 HG01978.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+2101delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148732345 | |||||
| chr7:148732353
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.140+2091T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732353 | ||||||
| chr7:148732404
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.140+2142A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732404 | ||||||
| chr7:148732417
|
A | G | 2 | a0001c0002t0001g0255a0001c0005t0001g0256 | 2 | HG00408.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.140+2155A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732417 | ||||||
| chr7:148732434
|
C | A | 6 | a0001c0001t0002g0162a0001c0001t0002g0206a0001c0001t0002g0207others(3): Show | 6 | HG01884.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+2172C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732434 | ||||||
| chr7:148732473
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+2211A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732473 | ||||||
| chr7:148732677
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.140+2415G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732677 | ||||||
| chr7:148732714
|
G | A | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 76 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.140+2452G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732714 | ||||||
| chr7:148732719
|
G | C | 5 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0327others(2): Show | 5 | HG01891.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+2457G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732719 | ||||||
| chr7:148732970
|
C | T | 138 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 138 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.140+2708C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732970 | ||||||
| chr7:148732976
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+2714G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732976 | ||||||
| chr7:148733027
|
G | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.140+2765G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733027 | ||||||
| chr7:148733028
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.140+2766C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733028 | ||||||
| chr7:148733029
|
T | G | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.140+2767T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733029 | ||||||
| chr7:148733056
|
A | C | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 94 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.140+2794A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733056 | ||||||
| chr7:148733118
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+2856C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733118 | ||||||
| chr7:148733172
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+2910G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733172 | ||||||
| chr7:148733267
|
G | C | 3 | a0001c0001t0002g0164a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG00735.hp1 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140+3005G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733267 | ||||||
| chr7:148733328
|
A | G | 15 | a0001c0001t0001g0092a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.140+3066A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733328 | ||||||
| chr7:148733545
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0188 | 2 | HG03239.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.140+3283G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733545 | ||||||
| chr7:148733661
|
G | GC | 11 | a0001c0001t0001g0092a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+3400dupC | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148733661 | |||||
| chr7:148733865
|
T | A | 1 | a0001c0001t0004g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.140+3603T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733865 | ||||||
| chr7:148734036
|
AAAAAG | A | 88 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 88 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.140+3789_140+3793d others(7): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148734036 | |||||
| chr7:148734218
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.140+3956A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148734218 | ||||||
| chr7:148734251
|
C | CTG | 5 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0242others(2): Show | 5 | HG00738.hp2 HG00741.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+4001_140+4002d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148734251 | |||||
| chr7:148734269
|
CAG | C | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+4010_140+4011d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148734269 | |||||
| chr7:148734375
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.140+4113C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148734375 | ||||||
| chr7:148734517
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.140+4255G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148734517 | ||||||
| chr7:148734666
|
C | T | 11 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(8): Show | 11 | HG01952.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+4404C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148734666 | ||||||
| chr7:148735118
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.140+4856G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735118 | ||||||
| chr7:148735203
|
C | T | 6 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+4941C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735203 | ||||||
| chr7:148735253
|
C | T | 11 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(8): Show | 11 | HG01952.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+4991C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735253 | ||||||
| chr7:148735369
|
C | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5107C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735369 | ||||||
| chr7:148735370
|
T | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5108T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735370 | ||||||
| chr7:148735372
|
C | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5110C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735372 | ||||||
| chr7:148735374
|
G | T | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5112G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735374 | ||||||
| chr7:148735375
|
C | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5113C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735375 | ||||||
| chr7:148735377
|
A | T | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5115A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735377 | ||||||
| chr7:148735379
|
C | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5117C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735379 | ||||||
| chr7:148735386
|
T | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5124T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735386 | ||||||
| chr7:148735387
|
T | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5125T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735387 | ||||||
| chr7:148735395
|
A | AGAGCTGT others(4): Show |
1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5133_140+5134i others(13): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735395 | ||||||
| chr7:148735399
|
T | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5137T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735399 | ||||||
| chr7:148735407
|
T | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5145T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735407 | ||||||
| chr7:148735423
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5161A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735423 | ||||||
| chr7:148735425
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5163G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735425 | ||||||
| chr7:148735426
|
A | C | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5164A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735426 | ||||||
| chr7:148735428
|
C | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5166C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735428 | ||||||
| chr7:148735433
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+5171C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735433 | ||||||
| chr7:148735442
|
A | G | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.140+5180A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735442 | ||||||
| chr7:148735443
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5181G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735443 | ||||||
| chr7:148735444
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5182T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735444 | ||||||
| chr7:148735445
|
G | T | 11 | a0001c0001t0001g0092a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+5183G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735445 | ||||||
| chr7:148735447
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5185T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735447 | ||||||
| chr7:148735453
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5191G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735453 | ||||||
| chr7:148735454
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.140+5192G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735454 | ||||||
| chr7:148735455
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.140+5193C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735455 | ||||||
| chr7:148735458
|
C | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5196C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735458 | ||||||
| chr7:148735460
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5198T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735460 | ||||||
| chr7:148735464
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5202T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735464 | ||||||
| chr7:148735469
|
C | T | 9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+5207C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735469 | ||||||
| chr7:148735517
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.140+5255A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735517 | ||||||
| chr7:148735866
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.140+5604C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735866 | ||||||
| chr7:148735924
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.140+5662G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735924 | ||||||
| chr7:148736007
|
T | TA | 7 | a0001c0001t0001g0091a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01074.hp1 HG01074.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.140+5765dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148736007 | |||||
| chr7:148736007
|
TA | T | 14 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(11): Show | 14 | HG01070.hp1 HG01070.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.140+5765delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148736007 | |||||
| chr7:148736007
|
TAAA | T | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(122): Show | 125 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.140+5763_140+5765d others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148736007 | |||||
| chr7:148736007
|
TAAAA | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0090others(10): Show | 13 | HG01168.hp1 HG02109.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+5762_140+5765d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148736007 | |||||
| chr7:148736486
|
A | G | 3 | a0001c0003t0001g0116a0001c0003t0001g0123a0001c0003t0001g0264 | 3 | HG02145.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.140+6224A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148736486 | ||||||
| chr7:148736542
|
G | A | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.140+6280G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148736542 | ||||||
| chr7:148736624
|
T | G | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0170others(1): Show | 4 | HG00280.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+6362T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148736624 | ||||||
| chr7:148736781
|
A | C | 1 | a0001c0003t0001g0123 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.140+6519A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148736781 | ||||||
| chr7:148736971
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0051 | 2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.140+6709G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148736971 | ||||||
| chr7:148736996
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.140+6734G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148736996 | ||||||
| chr7:148737130
|
A | C | 15 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 15 | HG01952.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.140+6868A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737130 | ||||||
| chr7:148737189
|
A | AT | 6 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0083others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+6941dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737189 | |||||
| chr7:148737269
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.140+7007G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737269 | ||||||
| chr7:148737359
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+7097C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737359 | ||||||
| chr7:148737402
|
T | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.140+7140T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737402 | ||||||
| chr7:148737508
|
G | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.140+7246G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737508 | ||||||
| chr7:148737560
|
A | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0327a0001c0001t0001g0328others(6): Show | 9 | HG02145.hp1 HG02165.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.140+7298A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737560 | ||||||
| chr7:148737571
|
T | TATA | 8 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0242others(5): Show | 8 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+7309_140+7310i others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737571 | ||||||
| chr7:148737572
|
T | A | 216 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(213): Show | 216 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.140+7310T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737572 | ||||||
| chr7:148737574
|
T | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02165.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.140+7312T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737574 | ||||||
| chr7:148737574
|
T | TATA | 8 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0242others(5): Show | 8 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+7312_140+7313i others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737574 | ||||||
| chr7:148737576
|
A | ATATT | 43 | a0001c0001t0001g0091a0001c0001t0001g0154a0001c0001t0001g0155others(40): Show | 43 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.140+7352_140+7355d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737576 | |||||
| chr7:148737576
|
A | ATATTTAT others(1): Show |
12 | a0001c0001t0001g0238a0001c0001t0001g0270a0001c0001t0001g0271others(9): Show | 12 | HG00423.hp2 HG01891.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.140+7348_140+7355d others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737576 | |||||
| chr7:148737576
|
A | T | 25 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0204others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.140+7314A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737576 | ||||||
| chr7:148737576
|
ATATT | A | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(77): Show | 80 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.140+7352_140+7355d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737576 | |||||
| chr7:148737576
|
ATATTTAT others(1): Show |
A | 46 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0092others(43): Show | 46 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.140+7348_140+7355d others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737576 | |||||
| chr7:148737576
|
ATATTTAT others(5): Show |
A | 2 | a0001c0001t0001g0083a0001c0001t0001g0294 | 2 | HG02135.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.140+7344_140+7355d others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737576 | |||||
| chr7:148737576
|
ATATTTAT others(13): Show |
A | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.140+7336_140+7355d others(22): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737576 | |||||
| chr7:148737578
|
A | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02165.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.140+7316A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737578 | ||||||
| chr7:148737580
|
T | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02165.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.140+7318T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737580 | ||||||
| chr7:148737789
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.140+7527C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737789 | ||||||
| chr7:148737806
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.140+7544C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737806 | ||||||
| chr7:148738005
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.140+7743C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738005 | ||||||
| chr7:148738183
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.140+7921A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738183 | ||||||
| chr7:148738247
|
A | G | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.140+7985A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738247 | ||||||
| chr7:148738301
|
A | G | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 143 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.140+8039A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738301 | ||||||
| chr7:148738334
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+8072G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738334 | ||||||
| chr7:148738557
|
G | A | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+8295G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738557 | ||||||
| chr7:148738683
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140+8421A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738683 | ||||||
| chr7:148738969
|
G | A | 3 | a0001c0001t0002g0164a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG00735.hp1 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140+8707G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738969 | ||||||
| chr7:148739014
|
G | C | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 94 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.140+8752G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739014 | ||||||
| chr7:148739346
|
G | T | 1 | a0001c0001t0001g0315 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.140+9084G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739346 | ||||||
| chr7:148739369
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.140+9107A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739369 | ||||||
| chr7:148739375
|
T | C | 1 | a0001c0001t0001g0032 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.140+9113T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739375 | ||||||
| chr7:148739417
|
A | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.140+9155A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739417 | ||||||
| chr7:148739437
|
C | T | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+9175C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739437 | ||||||
| chr7:148739449
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140+9187A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739449 | ||||||
| chr7:148739491
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+9229C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739491 | ||||||
| chr7:148739662
|
T | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG02109.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.140+9400T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739662 | ||||||
| chr7:148739876
|
C | G | 1 | a0001c0001t0001g0089 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.140+9614C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739876 | ||||||
| chr7:148739894
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.140+9632A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739894 | ||||||
| chr7:148739912
|
C | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.140+9650C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739912 | ||||||
| chr7:148740058
|
C | CT | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 96 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.140+9809dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148740058 | |||||
| chr7:148740113
|
C | T | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 94 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.140+9851C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148740113 | ||||||
| chr7:148740197
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140+9935C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148740197 | ||||||
| chr7:148740255
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.140+9993A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148740255 | ||||||
| chr7:148740391
|
T | C | 9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+10129T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148740391 | ||||||
| chr7:148740940
|
A | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.140+10678A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148740940 | ||||||
| chr7:148741053
|
C | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 103 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.140+10791C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741053 | ||||||
| chr7:148741180
|
CT | C | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 140 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.140+10923delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148741180 | |||||
| chr7:148741191
|
T | TA | 7 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(4): Show | 7 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.140+10930dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148741191 | |||||
| chr7:148741432
|
T | G | 1 | a0001c0001t0001g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.140+11170T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741432 | ||||||
| chr7:148741444
|
TTTAC | T | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.140+11190_140+1119 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148741444 | |||||
| chr7:148741497
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.140+11235G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741497 | ||||||
| chr7:148741541
|
CGATTCTC others(128): Show |
C | 137 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 137 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.140+11323_140+1145 others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148741541 | |||||
| chr7:148741563
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.140+11301C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741563 | ||||||
| chr7:148741574
|
A | G | 2 | a0001c0001t0001g0321a0001c0001t0001g0322 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.140+11312A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741574 | ||||||
| chr7:148741585
|
T | C | 79 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0080others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.140+11323T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741585 | ||||||
| chr7:148741698
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+11436C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741698 | ||||||
| chr7:148741710
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0271 | 3 | HG01978.hp2 HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140+11448A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741710 | ||||||
| chr7:148741712
|
C | T | 15 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0205others(12): Show | 15 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.140+11450C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741712 | ||||||
| chr7:148741832
|
C | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(2): Show | 5 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+11570C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741832 | ||||||
| chr7:148741870
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.140+11608G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741870 | ||||||
| chr7:148742029
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.140+11767T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742029 | ||||||
| chr7:148742117
|
T | A | 9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+11855T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742117 | ||||||
| chr7:148742182
|
T | G | 2 | a0001c0001t0001g0305a0001c0001t0001g0306 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.141-11794T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742182 | ||||||
| chr7:148742273
|
G | C | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(210): Show | 213 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.141-11703G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742273 | ||||||
| chr7:148742282
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.141-11694G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742282 | ||||||
| chr7:148742350
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.141-11626T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742350 | ||||||
| chr7:148742424
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0004g0120 | 3 | HG01891.hp1 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.141-11552G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742424 | ||||||
| chr7:148742589
|
C | G | 1 | a0001c0001t0001g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.141-11387C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742589 | ||||||
| chr7:148742598
|
G | GT | 10 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0183others(7): Show | 10 | HG01081.hp2 HG01928.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.141-11360dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | |||||
| chr7:148742598
|
G | GTTTTTTT others(2): Show |
45 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(42): Show | 45 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.141-11368_141-1136 others(13): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | |||||
| chr7:148742598
|
G | GTTTTTTT others(3): Show |
36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0013others(33): Show | 36 | HG00438.hp2 HG00639.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.141-11369_141-1136 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | |||||
| chr7:148742598
|
G | GTTTTTTT others(4): Show |
4 | a0001c0001t0001g0035a0001c0001t0001g0064a0001c0001t0001g0066others(1): Show | 4 | HG01361.hp2 HG03927.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-11370_141-1136 others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | |||||
| chr7:148742598
|
G | GTTTTTTT others(5): Show |
2 | a0001c0001t0001g0239a0001c0001t0001g0244 | 2 | HG00738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.141-11371_141-1136 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | |||||
| chr7:148742598
|
GT | G | 19 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(16): Show | 19 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.141-11360delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | |||||
| chr7:148742598
|
GTT | G | 35 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(32): Show | 35 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.141-11361_141-1136 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | |||||
| chr7:148742659
|
G | T | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 89 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.141-11317G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742659 | ||||||
| chr7:148742705
|
G | A | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(2): Show | 5 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-11271G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742705 | ||||||
| chr7:148742722
|
C | T | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-11254C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742722 | ||||||
| chr7:148742759
|
G | T | 5 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0116others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-11217G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742759 | ||||||
| chr7:148742807
|
T | G | 3 | a0001c0001t0001g0067a0001c0002t0001g0255a0001c0005t0001g0256 | 3 | HG00408.hp1 HG00621.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.141-11169T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742807 | ||||||
| chr7:148743012
|
C | T | 11 | a0001c0001t0001g0092a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.141-10964C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743012 | ||||||
| chr7:148743098
|
T | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00738.hp2 HG01175.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.141-10878T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743098 | ||||||
| chr7:148743196
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.141-10780C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743196 | ||||||
| chr7:148743197
|
T | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.141-10779T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743197 | ||||||
| chr7:148743243
|
C | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.141-10733C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743243 | ||||||
| chr7:148743484
|
A | G | 15 | a0001c0001t0001g0092a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.141-10492A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743484 | ||||||
| chr7:148743544
|
A | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-10432A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743544 | ||||||
| chr7:148743548
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.141-10428A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743548 | ||||||
| chr7:148743620
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.141-10356T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743620 | ||||||
| chr7:148743650
|
T | C | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.141-10326T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743650 | ||||||
| chr7:148743662
|
GGGAGGCC others(17): Show |
G | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0279 | 3 | HG01346.hp1 HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.141-10289_141-1026 others(28): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148743662 | |||||
| chr7:148743687
|
G | A | 1 | a0001c0002t0001g0280 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.141-10289G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743687 | ||||||
| chr7:148743723
|
T | C | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 89 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.141-10253T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743723 | ||||||
| chr7:148743773
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.141-10203C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743773 | ||||||
| chr7:148743794
|
G | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00738.hp2 HG01175.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.141-10182G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743794 | ||||||
| chr7:148743877
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.141-10099G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743877 | ||||||
| chr7:148743897
|
A | G | 9 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(6): Show | 9 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-10079A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743897 | ||||||
| chr7:148743900
|
T | C | 9 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(6): Show | 9 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-10076T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743900 | ||||||
| chr7:148744308
|
G | T | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 140 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.141-9668G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148744308 | ||||||
| chr7:148744397
|
A | AGT | 22 | a0001c0001t0001g0104a0001c0001t0001g0110a0001c0001t0001g0111others(19): Show | 22 | HG01168.hp2 HG02135.hp2 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.141-9539_141-9538d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | |||||
| chr7:148744397
|
A | AGTGT | 6 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0139others(3): Show | 6 | HG01433.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-9541_141-9538d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | |||||
| chr7:148744397
|
A | AGTGTGT | 3 | a0001c0001t0001g0168a0001c0001t0001g0201a0001c0001t0001g0253 | 3 | HG02055.hp2 HG02145.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.141-9543_141-9538d others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | |||||
| chr7:148744397
|
AGT | A | 41 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0037others(38): Show | 41 | HG00673.hp1 HG00738.hp2 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.141-9539_141-9538d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | |||||
| chr7:148744397
|
AGTGT | A | 49 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(46): Show | 49 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.141-9541_141-9538d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | |||||
| chr7:148744397
|
AGTGTGT | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(38): Show | 41 | HG00438.hp2 HG00639.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.141-9543_141-9538d others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | |||||
| chr7:148744397
|
AGTGTGTG others(1): Show |
A | 4 | a0001c0001t0001g0074a0001c0001t0001g0083a0001c0001t0001g0307others(1): Show | 4 | HG02155.hp1 HG02451.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-9545_141-9538d others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | |||||
| chr7:148744397
|
AGTGTGTG others(5): Show |
A | 9 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(6): Show | 9 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-9549_141-9538d others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | |||||
| chr7:148744397
|
AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.141-9551_141-9538d others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | |||||
| chr7:148744397
|
AGTGTGTG others(9): Show |
A | 2 | a0001c0002t0001g0255a0001c0005t0001g0256 | 2 | HG00408.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.141-9553_141-9538d others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | |||||
| chr7:148744397
|
AGTGTGTG others(11): Show |
A | 66 | a0001c0001t0001g0067a0001c0001t0001g0091a0001c0001t0001g0132others(63): Show | 66 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.141-9555_141-9538d others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | |||||
| chr7:148744574
|
G | T | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.141-9402G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148744574 | ||||||
| chr7:148744599
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.141-9377T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148744599 | ||||||
| chr7:148744666
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.141-9310A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148744666 | ||||||
| chr7:148744682
|
A | T | 2 | a0001c0003t0001g0102a0001c0003t0001g0103 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.141-9294A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148744682 | ||||||
| chr7:148744979
|
T | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-8997T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148744979 | ||||||
| chr7:148745008
|
T | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG00738.hp2 HG01175.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.141-8968T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745008 | ||||||
| chr7:148745119
|
G | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.141-8857G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745119 | ||||||
| chr7:148745200
|
G | C | 11 | a0001c0001t0001g0092a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.141-8776G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745200 | ||||||
| chr7:148745359
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.141-8617G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745359 | ||||||
| chr7:148745573
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.141-8403C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745573 | ||||||
| chr7:148745655
|
A | G | 17 | a0001c0001t0001g0067a0001c0001t0001g0272a0001c0001t0001g0294others(14): Show | 17 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.141-8321A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745655 | ||||||
| chr7:148745679
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.141-8297A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745679 | ||||||
| chr7:148745883
|
C | T | 5 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0116others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-8093C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745883 | ||||||
| chr7:148746040
|
G | A | 5 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0116others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-7936G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148746040 | ||||||
| chr7:148746064
|
A | G | 17 | a0001c0001t0001g0092a0001c0001t0001g0104a0001c0001t0001g0105others(14): Show | 17 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.141-7912A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148746064 | ||||||
| chr7:148746117
|
T | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0092others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-7859T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148746117 | ||||||
| chr7:148746369
|
C | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 104 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.141-7607C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148746369 | ||||||
| chr7:148746373
|
C | CA | 10 | a0001c0001t0001g0113a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 10 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.141-7602dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148746373 | |||||
| chr7:148746471
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.141-7505C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148746471 | ||||||
| chr7:148746968
|
C | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.141-7008C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148746968 | ||||||
| chr7:148747016
|
T | C | 22 | a0001c0001t0001g0020a0001c0001t0001g0083a0001c0001t0001g0117others(19): Show | 22 | HG00738.hp2 HG01175.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.141-6960T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747016 | ||||||
| chr7:148747089
|
A | G | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG00140.hp2 HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.141-6887A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747089 | ||||||
| chr7:148747114
|
C | T | 11 | a0001c0001t0001g0092a0001c0001t0001g0113a0001c0001t0001g0135others(8): Show | 11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.141-6862C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747114 | ||||||
| chr7:148747263
|
C | A | 21 | a0001c0001t0001g0083a0001c0001t0001g0117a0001c0001t0001g0118others(18): Show | 21 | HG00738.hp2 HG01175.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.141-6713C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747263 | ||||||
| chr7:148747344
|
T | C | 1 | a0001c0001t0001g0274 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.141-6632T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747344 | ||||||
| chr7:148747632
|
G | A | 32 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(29): Show | 32 | HG00738.hp2 HG01175.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.141-6344G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747632 | ||||||
| chr7:148747753
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.141-6223A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747753 | ||||||
| chr7:148747786
|
C | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 153 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.141-6190C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747786 | ||||||
| chr7:148747809
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.141-6167G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747809 | ||||||
| chr7:148747875
|
GATCATTG others(143): Show |
G | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-6098_141-5949d others(2): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148747875 | |||||
| chr7:148747981
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0051 | 2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.141-5995A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747981 | ||||||
| chr7:148748200
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.141-5776C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148748200 | ||||||
| chr7:148748377
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0122 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.141-5599G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148748377 | ||||||
| chr7:148748415
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.141-5561G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148748415 | ||||||
| chr7:148748561
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.141-5415C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148748561 | ||||||
| chr7:148748606
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.141-5370A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148748606 | ||||||
| chr7:148748716
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 221 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.141-5260T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148748716 | ||||||
| chr7:148749081
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(208): Show | 213 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.141-4895G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749081 | ||||||
| chr7:148749207
|
A | G | 2 | a0001c0001t0001g0260a0001c0001t0001g0295 | 2 | NA19004.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.141-4769A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749207 | ||||||
| chr7:148749245
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.141-4731C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749245 | ||||||
| chr7:148749262
|
C | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 79 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.141-4714C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749262 | ||||||
| chr7:148749285
|
T | A | 104 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(101): Show | 104 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.141-4691T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749285 | ||||||
| chr7:148749372
|
T | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 83 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.141-4604T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749372 | ||||||
| chr7:148749415
|
C | CA | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0034others(27): Show | 32 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.141-4541dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148749415 | |||||
| chr7:148749415
|
C | CAA | 10 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.141-4542_141-4541d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148749415 | |||||
| chr7:148749415
|
C | CAAA | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(99): Show | 102 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.141-4543_141-4541d others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148749415 | |||||
| chr7:148749415
|
C | CAAAA | 71 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(68): Show | 72 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.141-4544_141-4541d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148749415 | |||||
| chr7:148749415
|
C | CAAAAA | 14 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0038others(11): Show | 14 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.141-4545_141-4541d others(7): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148749415 | |||||
| chr7:148749556
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.141-4420C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749556 | ||||||
| chr7:148749557
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 82 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.141-4419G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749557 | ||||||
| chr7:148749557
|
G | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-4419G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749557 | ||||||
| chr7:148749605
|
T | A | 1 | a0001c0001t0001g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.141-4371T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749605 | ||||||
| chr7:148749819
|
A | G | 108 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(105): Show | 108 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.141-4157A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749819 | ||||||
| chr7:148749985
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.141-3991A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749985 | ||||||
| chr7:148750264
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.141-3712C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750264 | ||||||
| chr7:148750294
|
C | CT | 113 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(110): Show | 113 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.141-3666dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148750294 | |||||
| chr7:148750294
|
C | CTT | 6 | a0001c0001t0001g0071a0001c0001t0001g0126a0001c0001t0001g0127others(3): Show | 6 | HG01978.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-3667_141-3666d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148750294 | |||||
| chr7:148750294
|
CT | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0034others(21): Show | 26 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.141-3666delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148750294 | |||||
| chr7:148750311
|
A | T | 1 | a0001c0001t0001g0270 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.141-3665A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750311 | ||||||
| chr7:148750396
|
C | A | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-3580C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750396 | ||||||
| chr7:148750473
|
T | G | 1 | a0001c0001t0001g0155 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.141-3503T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750473 | ||||||
| chr7:148750658
|
C | T | 104 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(101): Show | 104 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.141-3318C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750658 | ||||||
| chr7:148750682
|
C | G | 10 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0165others(7): Show | 10 | HG00280.hp1 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.141-3294C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750682 | ||||||
| chr7:148750836
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0081 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.141-3140T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750836 | ||||||
| chr7:148750842
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.141-3134G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750842 | ||||||
| chr7:148750894
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.141-3082C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750894 | ||||||
| chr7:148750984
|
TA | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 96 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.141-2977delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148750984 | |||||
| chr7:148750984
|
TAA | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.141-2978_141-2977d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148750984 | |||||
| chr7:148750994
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.141-2982A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750994 | ||||||
| chr7:148750995
|
A | C | 1 | a0001c0001t0002g0164 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.141-2981A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750995 | ||||||
| chr7:148751119
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 83 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.141-2857G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751119 | ||||||
| chr7:148751129
|
A | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 82 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.141-2847A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751129 | ||||||
| chr7:148751161
|
C | A | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-2815C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751161 | ||||||
| chr7:148751353
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.141-2623A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751353 | ||||||
| chr7:148751420
|
C | G | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-2556C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751420 | ||||||
| chr7:148751421
|
G | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-2555G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751421 | ||||||
| chr7:148751422
|
C | G | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-2554C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751422 | ||||||
| chr7:148751459
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0187 | 2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.141-2517C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751459 | ||||||
| chr7:148751534
|
C | CA | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(97): Show | 100 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.141-2422dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148751534 | |||||
| chr7:148751534
|
C | CAA | 11 | a0001c0001t0001g0011a0001c0001t0001g0125a0001c0001t0001g0141others(8): Show | 11 | HG00423.hp2 HG00642.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.141-2423_141-2422d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148751534 | |||||
| chr7:148751534
|
CA | C | 6 | a0001c0001t0001g0066a0001c0001t0001g0150a0001c0001t0001g0152others(3): Show | 6 | HG03209.hp1 NA18941.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-2422delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148751534 | |||||
| chr7:148751551
|
A | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.141-2425A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751551 | ||||||
| chr7:148751563
|
G | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 82 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.141-2413G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751563 | ||||||
| chr7:148751584
|
T | G | 11 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(8): Show | 11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.141-2392T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751584 | ||||||
| chr7:148751832
|
T | C | 104 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(101): Show | 104 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.141-2144T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751832 | ||||||
| chr7:148752006
|
C | G | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-1970C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752006 | ||||||
| chr7:148752071
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 82 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.141-1905A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752071 | ||||||
| chr7:148752311
|
G | A | 77 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0091others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.141-1665G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752311 | ||||||
| chr7:148752373
|
G | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.141-1603G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752373 | ||||||
| chr7:148752384
|
AGTT | A | 28 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 28 | HG00738.hp2 HG01175.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.141-1588_141-1586d others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148752384 | |||||
| chr7:148752471
|
C | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.141-1505C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752471 | ||||||
| chr7:148752477
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.141-1499T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752477 | ||||||
| chr7:148752572
|
A | AT | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 82 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.141-1397dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148752572 | |||||
| chr7:148752749
|
T | C | 1 | a0001c0001t0001g0270 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.141-1227T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752749 | ||||||
| chr7:148753158
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.141-818C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148753158 | ||||||
| chr7:148753159
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0205a0001c0001t0001g0291 | 3 | NA18968.hp1 NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.141-817G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148753159 | ||||||
| chr7:148753255
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.141-721G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148753255 | ||||||
| chr7:148753429
|
C | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 198 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.141-547C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148753429 | ||||||
| chr7:148753477
|
G | GAT | 83 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(80): Show | 84 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.141-498_141-497dup others(2): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148753477 | |||||
| chr7:148753807
|
C | G | 1 | a0001c0001t0002g0233 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.141-169C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148753807 | ||||||
| chr7:148753914
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.141-62T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148753914 | ||||||
| chr7:148754264
|
C | T | 5 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0116others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+114C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754264 | ||||||
| chr7:148754424
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.315+274C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754424 | ||||||
| chr7:148754465
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.315+315G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754465 | ||||||
| chr7:148754504
|
G | A | 2 | a0001c0003t0001g0102a0001c0003t0001g0103 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.315+354G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754504 | ||||||
| chr7:148754624
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.315+474G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754624 | ||||||
| chr7:148754797
|
A | C | 5 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0116others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+647A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754797 | ||||||
| chr7:148754858
|
C | T | 5 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0116others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+708C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754858 | ||||||
| chr7:148754859
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0207 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.315+709G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754859 | ||||||
| chr7:148754900
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+750C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754900 | ||||||
| chr7:148754902
|
A | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+752A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754902 | ||||||
| chr7:148754904
|
A | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+754A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754904 | ||||||
| chr7:148755018
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0003g0166 | 2 | HG01074.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.315+868G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755018 | ||||||
| chr7:148755280
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+1130T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755280 | ||||||
| chr7:148755281
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+1131C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755281 | ||||||
| chr7:148755282
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+1132C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755282 | ||||||
| chr7:148755283
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+1133T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755283 | ||||||
| chr7:148755330
|
C | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 198 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.315+1180C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755330 | ||||||
| chr7:148755557
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(4): Show | 7 | HG01433.hp2 HG01952.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.315+1407G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755557 | ||||||
| chr7:148755662
|
A | T | 6 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0140others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-1321A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755662 | ||||||
| chr7:148755813
|
C | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 82 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.316-1170C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755813 | ||||||
| chr7:148755939
|
C | G | 3 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0244 | 3 | HG00738.hp2 HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.316-1044C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755939 | ||||||
| chr7:148756359
|
G | A | 2 | a0001c0001t0001g0305a0001c0001t0001g0306 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.316-624G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756359 | ||||||
| chr7:148756367
|
G | A | 2 | a0001c0001t0001g0305a0001c0001t0001g0306 | 2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.316-616G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756367 | ||||||
| chr7:148756421
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.316-562C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756421 | ||||||
| chr7:148756520
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(73): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.316-463A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756520 | ||||||
| chr7:148756595
|
C | G | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.316-388C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756595 | ||||||
| chr7:148756784
|
T | A | 5 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 5 | HG02647.hp1 HG02896.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.316-199T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756784 | ||||||
| chr7:148756904
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG01433.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.316-79G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756904 | ||||||
| chr7:148757676
|
T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 197 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.483+526T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148757676 | ||||||
| chr7:148757851
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.483+701T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148757851 | ||||||
| chr7:148757879
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.483+729A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148757879 | ||||||
| chr7:148757896
|
C | G | 21 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0272others(18): Show | 21 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.483+746C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148757896 | ||||||
| chr7:148757906
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | NA18993.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.483+756G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148757906 | ||||||
| chr7:148757948
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0212 | 2 | HG01168.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.483+798C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148757948 | ||||||
| chr7:148758021
|
G | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0207 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.483+871G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148758021 | ||||||
| chr7:148758022
|
T | C | 2 | a0001c0001t0002g0162a0001c0001t0002g0207 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.483+872T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148758022 | ||||||
| chr7:148758330
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.484-974G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148758330 | ||||||
| chr7:148758618
|
A | G | 3 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0244 | 3 | HG00738.hp2 HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.484-686A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148758618 | ||||||
| chr7:148759034
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.484-270C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148759034 | ||||||
| chr7:148759062
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 251 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.484-242C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148759062 | ||||||
| chr7:148759082
|
T | G | 3 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0244 | 3 | HG00738.hp2 HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.484-222T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148759082 | ||||||
| chr7:148759110
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.484-194G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148759110 | ||||||
| chr7:148759233
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0051 | 2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.484-71T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148759233 | ||||||
| chr7:148760572
|
A | G | 3 | a0001c0001t0001g0091a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG00741.hp2 HG01978.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.789+76A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760572 | ||||||
| chr7:148760683
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.789+187C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760683 | ||||||
| chr7:148760706
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.789+210G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760706 | ||||||
| chr7:148760751
|
G | C | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.789+255G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760751 | ||||||
| chr7:148760823
|
A | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.789+327A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760823 | ||||||
| chr7:148760834
|
T | G | 1 | a0001c0001t0001g0192 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.789+338T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760834 | ||||||
| chr7:148760913
|
G | C | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.789+417G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760913 | ||||||
| chr7:148761049
|
C | T | 3 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0244 | 3 | HG00738.hp2 HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.789+553C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761049 | ||||||
| chr7:148761092
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0022 | 3 | HG02056.hp1 NA18954.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.789+596C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761092 | ||||||
| chr7:148761382
|
G | A | 6 | a0001c0001t0001g0113a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 6 | HG01257.hp2 HG01261.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.789+886G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761382 | ||||||
| chr7:148761426
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.789+930G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761426 | ||||||
| chr7:148761435
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0167 | 2 | HG01074.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.789+939T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761435 | ||||||
| chr7:148761531
|
T | A | 17 | a0001c0001t0001g0260a0001c0001t0001g0273a0001c0001t0001g0274others(14): Show | 17 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.789+1035T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761531 | ||||||
| chr7:148761552
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(135): Show | 140 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.789+1056C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761552 | ||||||
| chr7:148761715
|
C | T | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG00597.hp2 NA18966.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.789+1219C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761715 | ||||||
| chr7:148761716
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.789+1220G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761716 | ||||||
| chr7:148761879
|
G | A | 6 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0140others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.789+1383G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761879 | ||||||
| chr7:148761996
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.789+1500G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761996 | ||||||
| chr7:148762557
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.789+2061C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148762557 | ||||||
| chr7:148762583
|
T | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0034others(20): Show | 25 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.789+2087T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148762583 | ||||||
| chr7:148762594
|
A | G | 7 | a0001c0001t0001g0083a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.789+2098A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148762594 | ||||||
| chr7:148762880
|
C | T | 4 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+2384C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148762880 | ||||||
| chr7:148762934
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.789+2438G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148762934 | ||||||
| chr7:148762937
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.789+2441G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148762937 | ||||||
| chr7:148763017
|
G | T | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG01257.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.789+2521G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763017 | ||||||
| chr7:148763020
|
G | A | 2 | a0001c0002t0001g0278a0001c0002t0001g0309 | 2 | NA18955.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.789+2524G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763020 | ||||||
| chr7:148763022
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.789+2526C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763022 | ||||||
| chr7:148763152
|
A | T | 10 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+2656A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763152 | ||||||
| chr7:148763158
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.789+2662T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763158 | ||||||
| chr7:148763180
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | HG02109.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.789+2684C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763180 | ||||||
| chr7:148763183
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.789+2687G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763183 | ||||||
| chr7:148763218
|
T | A | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.789+2722T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763218 | ||||||
| chr7:148763397
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.789+2901C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763397 | ||||||
| chr7:148763424
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.789+2928A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763424 | ||||||
| chr7:148763444
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0034others(21): Show | 26 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.789+2948T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763444 | ||||||
| chr7:148763500
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.789+3004A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763500 | ||||||
| chr7:148763751
|
A | G | 1 | a0001c0001t0004g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.790-2810A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763751 | ||||||
| chr7:148763757
|
T | G | 1 | a0001c0001t0001g0275 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.790-2804T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763757 | ||||||
| chr7:148763862
|
A | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.790-2699A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763862 | ||||||
| chr7:148763910
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.790-2651C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763910 | ||||||
| chr7:148764010
|
GT | G | 12 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(9): Show | 12 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.790-2548delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr7 | 148764010 | |||||
| chr7:148764058
|
A | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.790-2503A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148764058 | ||||||
| chr7:148764327
|
T | G | 1 | a0001c0001t0001g0326 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.790-2234T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148764327 | ||||||
| chr7:148764504
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.790-2057G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148764504 | ||||||
| chr7:148764753
|
T | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.790-1808T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148764753 | ||||||
| chr7:148764977
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.790-1584C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148764977 | ||||||
| chr7:148764990
|
T | G | 1 | a0001c0001t0001g0298 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.790-1571T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148764990 | ||||||
| chr7:148765058
|
G | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(13): Show | 16 | HG01433.hp2 HG01952.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.790-1503G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765058 | ||||||
| chr7:148765085
|
A | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(3): Show | 6 | HG00741.hp1 HG01081.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.790-1476A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765085 | ||||||
| chr7:148765268
|
C | A | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.790-1293C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765268 | ||||||
| chr7:148765309
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.790-1252C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765309 | ||||||
| chr7:148765401
|
A | G | 80 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0094others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.790-1160A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765401 | ||||||
| chr7:148765519
|
G | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.790-1042G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765519 | ||||||
| chr7:148765628
|
T | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0074a0001c0001t0001g0075 | 3 | NA18951.hp1 NA18993.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.790-933T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765628 | ||||||
| chr7:148765726
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.790-835A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765726 | ||||||
| chr7:148765766
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.790-795T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765766 | ||||||
| chr7:148765999
|
T | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(135): Show | 140 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.790-562T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765999 | ||||||
| chr7:148766049
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.790-512C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148766049 | ||||||
| chr7:148766088
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.790-473A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148766088 | ||||||
| chr7:148766206
|
C | CTA | 75 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0094others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.790-353_790-352dup others(2): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr7 | 148766206 | |||||
| chr7:148766375
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0070others(93): Show | 97 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.790-186T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148766375 | ||||||
| chr7:148766768
|
T | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(255): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.952+45T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 8/21 | chr7 | 148766768 | ||||||
| chr7:148766845
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.952+122T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 8/21 | chr7 | 148766845 | ||||||
| chr7:148766967
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.952+244C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 8/21 | chr7 | 148766967 | ||||||
| chr7:148767328
|
A | AT | 47 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0086others(44): Show | 47 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.953-279dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 148767328 | |||||
| chr7:148767374
|
G | A | 13 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.953-245G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 8/21 | chr7 | 148767374 | ||||||
| chr7:148767583
|
T | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(255): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.953-36T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 8/21 | chr7 | 148767583 | ||||||
| chr7:148767942
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | NA19072.hp1 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1083+193C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148767942 | ||||||
| chr7:148767945
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+196C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148767945 | ||||||
| chr7:148767957
|
G | C | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+208G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148767957 | ||||||
| chr7:148768051
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1083+302G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768051 | ||||||
| chr7:148768067
|
A | C | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0170others(1): Show | 4 | HG00280.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+318A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768067 | ||||||
| chr7:148768067
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1083+318A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768067 | ||||||
| chr7:148768105
|
A | G | 11 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(8): Show | 11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1083+356A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768105 | ||||||
| chr7:148768378
|
C | CTTTTTTT | 7 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0131others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083+647_1083+653d others(9): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148768378 | |||||
| chr7:148768378
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1083+641_1083+653d others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148768378 | |||||
| chr7:148768378
|
CT | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 66 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1083+653delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148768378 | |||||
| chr7:148768378
|
CTTTT | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(156): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1083+650_1083+653d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148768378 | |||||
| chr7:148768378
|
CTTTTT | C | 67 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0017others(64): Show | 67 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.1083+649_1083+653d others(7): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148768378 | |||||
| chr7:148768378
|
CTTTTTT | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0237others(9): Show | 12 | HG00738.hp2 HG01175.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+648_1083+653d others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148768378 | |||||
| chr7:148768628
|
G | A | 9 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(6): Show | 9 | HG02647.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1083+879G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768628 | ||||||
| chr7:148768632
|
G | A | 12 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(9): Show | 12 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+883G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768632 | ||||||
| chr7:148768676
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0081 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1083+927C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768676 | ||||||
| chr7:148768719
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1083+970C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768719 | ||||||
| chr7:148768777
|
G | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(3): Show | 6 | HG00741.hp1 HG01081.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+1028G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768777 | ||||||
| chr7:148768881
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1083+1132C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768881 | ||||||
| chr7:148768896
|
T | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(131): Show | 136 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.1083+1147T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768896 | ||||||
| chr7:148768976
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1083+1227C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768976 | ||||||
| chr7:148769026
|
G | C | 24 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(21): Show | 24 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1083+1277G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769026 | ||||||
| chr7:148769027
|
A | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+1278A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769027 | ||||||
| chr7:148769033
|
C | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+1284C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769033 | ||||||
| chr7:148769101
|
G | A | 12 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(9): Show | 12 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+1352G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769101 | ||||||
| chr7:148769151
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1083+1402G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769151 | ||||||
| chr7:148769192
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1083+1443T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769192 | ||||||
| chr7:148769199
|
G | A | 17 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(14): Show | 17 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1083+1450G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769199 | ||||||
| chr7:148769371
|
C | T | 1 | a0001c0005t0001g0256 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1083+1622C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769371 | ||||||
| chr7:148769397
|
T | TCA | 30 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0033others(27): Show | 30 | HG00558.hp2 HG01258.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1083+1699_1083+170 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
T | TCACA | 37 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(34): Show | 38 | HG00423.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1083+1697_1083+170 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
T | TCACACA | 12 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(9): Show | 12 | HG00609.hp1 HG01358.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.1083+1695_1083+170 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
T | TCACACAC others(1): Show |
22 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0037others(19): Show | 22 | HG00621.hp2 HG01433.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1083+1693_1083+170 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
T | TCACACAC others(3): Show |
3 | a0001c0001t0001g0025a0001c0001t0001g0266a0001c0001t0002g0206 | 3 | HG02896.hp2 NA18906.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1083+1691_1083+170 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
T | TCACACAC others(5): Show |
1 | a0001c0001t0001g0204 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1083+1689_1083+170 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
T | TCACACAC others(7): Show |
5 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0047others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1083+1687_1083+170 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
T | TCACACAC others(9): Show |
1 | a0001c0001t0001g0048 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1083+1685_1083+170 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
T | TCACACAC others(11): Show |
1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1083+1683_1083+170 others(22): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
TCA | T | 47 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0023others(44): Show | 47 | HG00597.hp2 HG00621.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.1083+1699_1083+170 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
TCACA | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(43): Show | 48 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1083+1697_1083+170 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
TCACACA | T | 19 | a0001c0001t0001g0040a0001c0001t0001g0117a0001c0001t0001g0118others(16): Show | 19 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1083+1695_1083+170 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
TCACACAC others(1): Show |
T | 34 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0092others(31): Show | 34 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1083+1693_1083+170 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
TCACACAC others(3): Show |
T | 7 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(4): Show | 7 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083+1691_1083+170 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
TCACACAC others(5): Show |
T | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1083+1689_1083+170 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
TCACACAC others(9): Show |
T | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0330 | 3 | NA18971.hp1 NA18986.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1083+1685_1083+170 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769397
|
TCACACAC others(11): Show |
T | 1 | a0001c0001t0001g0311 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1083+1683_1083+170 others(22): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | |||||
| chr7:148769444
|
CACACA | C | 4 | a0001c0001t0001g0121a0001c0001t0001g0165a0001c0001t0001g0274others(1): Show | 4 | HG00408.hp2 HG02055.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+1697_1083+170 others(9): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769444 | |||||
| chr7:148769450
|
A | C | 1 | a0001c0001t0001g0239 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1083+1701A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769450 | ||||||
| chr7:148769458
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1083+1709A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769458 | ||||||
| chr7:148769787
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1083+2038C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769787 | ||||||
| chr7:148769931
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1083+2182C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769931 | ||||||
| chr7:148770355
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0034others(21): Show | 26 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.1083+2606T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770355 | ||||||
| chr7:148770373
|
A | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+2624A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770373 | ||||||
| chr7:148770510
|
C | G | 1 | a0001c0001t0001g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1083+2761C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770510 | ||||||
| chr7:148770582
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1083+2833C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770582 | ||||||
| chr7:148770585
|
T | C | 17 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(14): Show | 17 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1083+2836T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770585 | ||||||
| chr7:148770631
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1083+2882C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770631 | ||||||
| chr7:148770632
|
G | A | 12 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(9): Show | 12 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+2883G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770632 | ||||||
| chr7:148770673
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1083+2924C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770673 | ||||||
| chr7:148770726
|
C | T | 3 | a0001c0001t0001g0185a0001c0001t0001g0219a0001c0001t0001g0221 | 3 | HG00597.hp2 HG00639.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1083+2977C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770726 | ||||||
| chr7:148770818
|
A | C | 1 | a0001c0001t0001g0272 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1083+3069A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770818 | ||||||
| chr7:148770936
|
C | T | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(254): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1083+3187C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770936 | ||||||
| chr7:148771031
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0207 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1083+3282G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771031 | ||||||
| chr7:148771352
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1083+3603A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771352 | ||||||
| chr7:148771353
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1083+3604C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771353 | ||||||
| chr7:148771357
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1083+3608T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771357 | ||||||
| chr7:148771429
|
T | C | 1 | a0001c0001t0001g0324 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1083+3680T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771429 | ||||||
| chr7:148771525
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(129): Show | 134 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.1083+3776C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771525 | ||||||
| chr7:148771554
|
G | T | 4 | a0001c0001t0001g0089a0001c0001t0001g0175a0001c0001t0001g0181others(1): Show | 4 | NA18955.hp1 NA18984.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+3805G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771554 | ||||||
| chr7:148771830
|
A | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+4081A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771830 | ||||||
| chr7:148771943
|
C | T | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | NA18975.hp1 NA19065.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1083+4194C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771943 | ||||||
| chr7:148772093
|
A | G | 11 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(8): Show | 11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1083+4344A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772093 | ||||||
| chr7:148772136
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0051 | 2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1083+4387C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772136 | ||||||
| chr7:148772140
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1083+4391C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772140 | ||||||
| chr7:148772278
|
G | A | 1 | a0001c0001t0001g0330 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1083+4529G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772278 | ||||||
| chr7:148772289
|
C | T | 12 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(9): Show | 12 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+4540C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772289 | ||||||
| chr7:148772347
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1083+4598G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772347 | ||||||
| chr7:148772420
|
A | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(221): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1083+4671A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772420 | ||||||
| chr7:148772425
|
C | CA | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(238): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1083+4687dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148772425 | |||||
| chr7:148772425
|
C | CAA | 12 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(9): Show | 12 | HG02155.hp2 HG02257.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1083+4686_1083+468 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148772425 | |||||
| chr7:148772429
|
A | AC | 3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0115 | 3 | HG02109.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1083+4680_1083+468 others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772429 | ||||||
| chr7:148772515
|
A | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+4766A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772515 | ||||||
| chr7:148772624
|
C | T | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(254): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1083+4875C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772624 | ||||||
| chr7:148772737
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1083+4988G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772737 | ||||||
| chr7:148772743
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1083+4994A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772743 | ||||||
| chr7:148772828
|
G | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+5079G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772828 | ||||||
| chr7:148772905
|
C | T | 9 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1083+5156C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772905 | ||||||
| chr7:148773068
|
C | A | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(217): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1083+5319C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773068 | ||||||
| chr7:148773227
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(135): Show | 140 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.1083+5478C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773227 | ||||||
| chr7:148773268
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0321others(2): Show | 6 | HG00280.hp2 HG01071.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+5519A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773268 | ||||||
| chr7:148773321
|
T | C | 3 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0244 | 3 | HG00738.hp2 HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1083+5572T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773321 | ||||||
| chr7:148773383
|
C | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG02257.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1083+5634C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773383 | ||||||
| chr7:148773406
|
A | G | 106 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(103): Show | 106 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1083+5657A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773406 | ||||||
| chr7:148773547
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1083+5798C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773547 | ||||||
| chr7:148773626
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1083+5877G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773626 | ||||||
| chr7:148773657
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0112a0001c0001t0001g0125others(1): Show | 4 | HG01952.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+5908G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773657 | ||||||
| chr7:148773901
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1083+6152C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773901 | ||||||
| chr7:148773957
|
T | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0257 | 2 | HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1083+6208T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773957 | ||||||
| chr7:148774069
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1083+6320G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774069 | ||||||
| chr7:148774143
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+6394C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774143 | ||||||
| chr7:148774145
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1083+6396T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774145 | ||||||
| chr7:148774237
|
A | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG02257.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1083+6488A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774237 | ||||||
| chr7:148774492
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1083+6743C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774492 | ||||||
| chr7:148774551
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1083+6802A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774551 | ||||||
| chr7:148774639
|
A | C | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1083+6890A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774639 | ||||||
| chr7:148774669
|
G | A | 5 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0116others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083+6920G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774669 | ||||||
| chr7:148774713
|
A | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+6964A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774713 | ||||||
| chr7:148774746
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG03017.hp1 HG03490.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083+6997C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774746 | ||||||
| chr7:148774747
|
T | G | 3 | a0001c0003t0001g0116a0001c0003t0001g0123a0001c0003t0001g0264 | 3 | HG02145.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1083+6998T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774747 | ||||||
| chr7:148774998
|
A | G | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02647.hp2 HG03209.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+7249A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774998 | ||||||
| chr7:148775461
|
T | C | 24 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(21): Show | 24 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1083+7712T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148775461 | ||||||
| chr7:148775766
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+8017C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148775766 | ||||||
| chr7:148775811
|
T | G | 1 | a0001c0001t0001g0047 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1084-7972T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148775811 | ||||||
| chr7:148775855
|
G | GA | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(125): Show | 130 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.1084-7913dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148775855 | |||||
| chr7:148775855
|
GA | G | 17 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(14): Show | 17 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1084-7913delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148775855 | |||||
| chr7:148776051
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0063a0001c0001t0001g0068 | 3 | HG00558.hp1 NA18992.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1084-7732G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776051 | ||||||
| chr7:148776092
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1084-7691A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776092 | ||||||
| chr7:148776177
|
A | AC | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(225): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1084-7600dupC | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776177 | |||||
| chr7:148776214
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0184 | 2 | HG00280.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1084-7569C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776214 | ||||||
| chr7:148776292
|
TCTAACAT others(7): Show |
T | 1 | a0001c0001t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1084-7488_1084-747 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776292 | |||||
| chr7:148776292
|
TCTAACAT others(8): Show |
T | 2 | a0001c0001t0001g0261a0001c0001t0001g0266 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1084-7490_1084-747 others(19): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776292 | ||||||
| chr7:148776293
|
C | T | 1 | a0001c0001t0004g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1084-7490C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776293 | ||||||
| chr7:148776294
|
TAACATAA others(6): Show |
T | 1 | a0001c0001t0004g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1084-7488_1084-747 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776294 | ||||||
| chr7:148776307
|
C | CT | 21 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0022others(18): Show | 21 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1084-7449dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTT | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0038others(37): Show | 40 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1084-7454_1084-744 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT | 49 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0034others(46): Show | 50 | HG00140.hp1 HG00642.hp1 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.1084-7455_1084-744 others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(1): Show |
26 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0108others(23): Show | 27 | HG00280.hp2 HG01071.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1084-7456_1084-744 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(2): Show |
19 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0098others(16): Show | 19 | HG00597.hp2 HG01070.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1084-7457_1084-744 others(13): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(3): Show |
20 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0070others(17): Show | 20 | HG00597.hp1 HG01109.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1084-7458_1084-744 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(4): Show |
23 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(20): Show | 23 | HG00280.hp1 HG00408.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1084-7459_1084-744 others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0145a0001c0001t0001g0184a0001c0001t0001g0229others(5): Show | 8 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084-7460_1084-744 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(6): Show |
5 | a0001c0001t0001g0009a0001c0001t0001g0106a0001c0001t0001g0180others(2): Show | 5 | HG01168.hp2 HG02559.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084-7461_1084-744 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0273a0001c0001t0001g0312 | 2 | HG02040.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1084-7462_1084-744 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(8): Show |
8 | a0001c0001t0001g0012a0001c0001t0001g0188a0001c0001t0001g0275others(5): Show | 8 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084-7463_1084-744 others(19): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(9): Show |
9 | a0001c0001t0001g0277a0001c0001t0001g0281a0001c0001t0001g0287others(6): Show | 9 | HG00140.hp2 HG00642.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1084-7464_1084-744 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0274a0001c0001t0001g0295 | 2 | NA19004.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1084-7465_1084-744 others(21): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0001g0260a0001c0001t0001g0297 | 2 | HG03239.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1084-7467_1084-744 others(23): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0250 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1084-7469_1084-744 others(25): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0165 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1084-7474_1084-744 others(30): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0296 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1084-7449_1084-744 others(33): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1084-7476C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776307 | ||||||
| chr7:148776307
|
CTTTTTT | C | 11 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(8): Show | 11 | HG01175.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1084-7454_1084-744 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776307
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0310 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1084-7463_1084-744 others(19): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | |||||
| chr7:148776385
|
C | T | 16 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(13): Show | 16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-7398C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776385 | ||||||
| chr7:148776420
|
G | A | 84 | a0001c0001t0001g0016a0001c0001t0001g0035a0001c0001t0001g0038others(81): Show | 84 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.1084-7363G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776420 | ||||||
| chr7:148776617
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | HG02109.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1084-7166G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776617 | ||||||
| chr7:148776661
|
A | G | 7 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0194others(4): Show | 7 | HG02040.hp1 HG02523.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.1084-7122A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776661 | ||||||
| chr7:148776755
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1084-7028T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776755 | ||||||
| chr7:148776834
|
T | A | 1 | a0001c0001t0001g0298 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1084-6949T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776834 | ||||||
| chr7:148776962
|
C | T | 16 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(13): Show | 16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-6821C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776962 | ||||||
| chr7:148777049
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1084-6734A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777049 | ||||||
| chr7:148777067
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1084-6716G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777067 | ||||||
| chr7:148777171
|
G | A | 9 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0073others(6): Show | 9 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.1084-6612G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777171 | ||||||
| chr7:148777174
|
G | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(256): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1084-6609G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777174 | ||||||
| chr7:148777194
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1084-6589A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777194 | ||||||
| chr7:148777267
|
T | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1084-6516T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777267 | ||||||
| chr7:148777377
|
G | A | 17 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(14): Show | 17 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1084-6406G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777377 | ||||||
| chr7:148777506
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0100 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1084-6277G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777506 | ||||||
| chr7:148777618
|
T | G | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1084-6165T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777618 | ||||||
| chr7:148777654
|
A | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(225): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1084-6129A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777654 | ||||||
| chr7:148777660
|
C | T | 11 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(8): Show | 11 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084-6123C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777660 | ||||||
| chr7:148777744
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0134 | 2 | HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1084-6039T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777744 | ||||||
| chr7:148778022
|
C | T | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1084-5761C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778022 | ||||||
| chr7:148778070
|
C | CA | 11 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0023others(8): Show | 11 | HG00558.hp2 HG02300.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084-5686dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAA | 10 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(7): Show | 10 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-5687_1084-568 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAA | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0112others(4): Show | 9 | HG01167.hp2 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1084-5690_1084-568 others(9): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAA | 9 | a0001c0001t0001g0111a0001c0001t0001g0132a0001c0001t0001g0146others(6): Show | 9 | HG01071.hp1 HG01169.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1084-5691_1084-568 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA | 10 | a0001c0001t0001g0010a0001c0001t0001g0072a0001c0001t0001g0098others(7): Show | 10 | HG01070.hp1 HG01070.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-5692_1084-568 others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(1): Show |
23 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0071others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1084-5693_1084-568 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(2): Show |
28 | a0001c0001t0001g0070a0001c0001t0001g0083a0001c0001t0001g0099others(25): Show | 28 | HG00423.hp2 HG00639.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1084-5694_1084-568 others(13): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(3): Show |
30 | a0001c0001t0001g0034a0001c0001t0001g0067a0001c0001t0001g0100others(27): Show | 30 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1084-5695_1084-568 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(4): Show |
28 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 28 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1084-5696_1084-568 others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(5): Show |
8 | a0001c0001t0001g0035a0001c0001t0001g0090a0001c0001t0001g0158others(5): Show | 8 | HG00642.hp1 HG00673.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1084-5697_1084-568 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0003t0001g0102 | 3 | HG03225.hp1 NA18941.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1084-5698_1084-568 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0016a0001c0001t0001g0163a0001c0001t0001g0230 | 3 | HG02559.hp1 HG03942.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1084-5699_1084-568 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(8): Show |
9 | a0001c0001t0001g0092a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG01071.hp2 HG01109.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-5700_1084-568 others(19): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | NA18943.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1084-5701_1084-568 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0118 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1084-5702_1084-568 others(21): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(11): Show |
4 | a0001c0001t0001g0095a0001c0001t0001g0108a0001c0001t0001g0121others(1): Show | 4 | HG01123.hp2 HG02055.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-5703_1084-568 others(22): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0154a0001c0001t0001g0314 | 2 | HG01993.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1084-5704_1084-568 others(23): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(13): Show |
4 | a0001c0001t0001g0153a0001c0001t0001g0238a0001c0001t0002g0162others(1): Show | 4 | HG01884.hp2 NA18953.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-5705_1084-568 others(24): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(14): Show |
2 | a0001c0001t0001g0089a0001c0001t0001g0247 | 2 | NA18984.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1084-5706_1084-568 others(25): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0001g0147a0001c0004t0001g0211 | 2 | HG02135.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1084-5707_1084-568 others(26): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1084-5708_1084-568 others(27): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1084-5709_1084-568 others(28): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(18): Show |
3 | a0001c0001t0001g0114a0001c0001t0001g0122a0001c0001t0001g0175 | 3 | HG01243.hp2 NA19011.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1084-5710_1084-568 others(29): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0279 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1084-5686_1084-568 others(35): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778070
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0335 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1084-5686_1084-568 others(36): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | |||||
| chr7:148778083
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0148 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1084-5697_1084-568 others(19): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778083 | |||||
| chr7:148778085
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1084-5695_1084-568 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778085 | |||||
| chr7:148778088
|
AAAAAAAA others(3): Show |
A | 16 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(13): Show | 16 | HG01952.hp1 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-5692_1084-568 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778088 | |||||
| chr7:148778094
|
AAAAG | A | 10 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(7): Show | 10 | HG02080.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-5686_1084-568 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778094 | |||||
| chr7:148778095
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1084-5688A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778095 | ||||||
| chr7:148778097
|
AG | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG02647.hp2 HG03209.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-5685delG | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778097 | ||||||
| chr7:148778098
|
G | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(181): Show | 186 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1084-5685G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778098 | ||||||
| chr7:148778101
|
G | A | 1 | a0001c0004t0001g0211 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1084-5682G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778101 | ||||||
| chr7:148778103
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1084-5680A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778103 | ||||||
| chr7:148778272
|
A | G | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1084-5511A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778272 | ||||||
| chr7:148778349
|
G | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG02257.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1084-5434G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778349 | ||||||
| chr7:148778365
|
G | A | 10 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 10 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-5418G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778365 | ||||||
| chr7:148778436
|
A | G | 19 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(16): Show | 19 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1084-5347A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778436 | ||||||
| chr7:148778571
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1084-5212C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778571 | ||||||
| chr7:148778572
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1084-5211G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778572 | ||||||
| chr7:148778745
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1084-5038C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778745 | ||||||
| chr7:148778836
|
G | T | 28 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0144others(25): Show | 28 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1084-4947G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778836 | ||||||
| chr7:148779024
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1084-4759A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779024 | ||||||
| chr7:148779278
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1084-4505A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779278 | ||||||
| chr7:148779563
|
G | C | 1 | a0001c0001t0001g0022 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1084-4220G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779563 | ||||||
| chr7:148779641
|
A | G | 10 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 10 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-4142A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779641 | ||||||
| chr7:148779669
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1084-4114C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779669 | ||||||
| chr7:148779838
|
AGTGGGCT others(27): Show |
A | 1 | a0001c0001t0001g0294 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1084-3938_1084-390 others(38): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148779838 | |||||
| chr7:148779970
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0081 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1084-3813A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779970 | ||||||
| chr7:148779996
|
G | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(236): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1084-3787G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779996 | ||||||
| chr7:148780079
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1084-3704T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148780079 | ||||||
| chr7:148780113
|
GTA | G | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(235): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1084-3658_1084-365 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148780113 | |||||
| chr7:148780211
|
A | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(3): Show | 6 | HG00741.hp1 HG01081.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1084-3572A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148780211 | ||||||
| chr7:148780388
|
T | G | 10 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 10 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-3395T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148780388 | ||||||
| chr7:148780497
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(131): Show | 136 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.1084-3286G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148780497 | ||||||
| chr7:148780663
|
G | A | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG00642.hp2 HG01192.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084-3120G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148780663 | ||||||
| chr7:148780747
|
A | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0026others(4): Show | 8 | HG00423.hp1 HG00438.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.1084-3036A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148780747 | ||||||
| chr7:148781079
|
A | AT | 10 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0022others(7): Show | 10 | HG01167.hp1 HG02602.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-2682dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | |||||
| chr7:148781079
|
A | ATTTTT | 7 | a0001c0001t0001g0011a0001c0001t0001g0070a0001c0001t0001g0071others(4): Show | 7 | HG00408.hp2 HG01433.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1084-2686_1084-268 others(9): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | |||||
| chr7:148781079
|
A | ATTTTTT | 65 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0072others(62): Show | 65 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1084-2687_1084-268 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | |||||
| chr7:148781079
|
A | ATTTTTTT | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(104): Show | 109 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1084-2688_1084-268 others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | |||||
| chr7:148781079
|
A | ATTTTTTT others(1): Show |
60 | a0001c0001t0001g0016a0001c0001t0001g0035a0001c0001t0001g0049others(57): Show | 60 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1084-2689_1084-268 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | |||||
| chr7:148781079
|
A | ATTTTTTT others(2): Show |
14 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0113others(11): Show | 14 | HG00738.hp1 HG01175.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1084-2690_1084-268 others(13): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | |||||
| chr7:148781079
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1084-2692_1084-268 others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | |||||
| chr7:148781079
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1084-2693_1084-268 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | |||||
| chr7:148781079
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0004g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1084-2694_1084-268 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | |||||
| chr7:148781109
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0034others(22): Show | 27 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1084-2674T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781109 | ||||||
| chr7:148781117
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1084-2666C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781117 | ||||||
| chr7:148781123
|
C | T | 68 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0095others(65): Show | 68 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1084-2660C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781123 | ||||||
| chr7:148781126
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1084-2657G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781126 | ||||||
| chr7:148781173
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG00741.hp2 HG01978.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1084-2610C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781173 | ||||||
| chr7:148781302
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1084-2481A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781302 | ||||||
| chr7:148781408
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1084-2375T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781408 | ||||||
| chr7:148781628
|
T | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(256): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1084-2155T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781628 | ||||||
| chr7:148781761
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1084-2022C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781761 | ||||||
| chr7:148781803
|
C | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(237): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1084-1980C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781803 | ||||||
| chr7:148781890
|
G | A | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1084-1893G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781890 | ||||||
| chr7:148781959
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1084-1824A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781959 | ||||||
| chr7:148781979
|
G | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(236): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1084-1804G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781979 | ||||||
| chr7:148782078
|
G | A | 10 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 10 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-1705G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782078 | ||||||
| chr7:148782107
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1084-1676G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782107 | ||||||
| chr7:148782201
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1084-1582C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782201 | ||||||
| chr7:148782225
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1084-1558C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782225 | ||||||
| chr7:148782556
|
T | A | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(220): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1084-1227T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782556 | ||||||
| chr7:148782556
|
T | G | 11 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(8): Show | 11 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084-1227T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782556 | ||||||
| chr7:148782591
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1084-1192T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782591 | ||||||
| chr7:148782643
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1084-1140T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782643 | ||||||
| chr7:148782657
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1084-1126A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782657 | ||||||
| chr7:148782822
|
G | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG00558.hp2 NA18943.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1084-961G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782822 | ||||||
| chr7:148782846
|
GC | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(221): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1084-936delC | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782846 | ||||||
| chr7:148782879
|
C | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG02257.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1084-904C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782879 | ||||||
| chr7:148782884
|
A | G | 16 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(13): Show | 16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-899A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782884 | ||||||
| chr7:148783022
|
G | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(236): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1084-761G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148783022 | ||||||
| chr7:148783141
|
C | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(234): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1084-642C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148783141 | ||||||
| chr7:148783173
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1084-610C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148783173 | ||||||
| chr7:148783182
|
C | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0001g0330 | 3 | HG02523.hp2 NA18961.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1084-601C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148783182 | ||||||
| chr7:148783377
|
C | A | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0251others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-406C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148783377 | ||||||
| chr7:148783667
|
A | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1084-116A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148783667 | ||||||
| chr7:148783898
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(151): Show | 156 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(153): Show |
splice_region_variant&intron_variant | LOW | c.1191+8C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 10/21 | chr7 | 148783898 | ||||||
| chr7:148783952
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1192-19T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 10/21 | chr7 | 148783952 | ||||||
| chr7:148784167
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1298+90C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784167 | ||||||
| chr7:148784396
|
G | A | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(232): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1298+319G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784396 | ||||||
| chr7:148784547
|
T | A | 8 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1298+470T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784547 | ||||||
| chr7:148784559
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1298+482G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784559 | ||||||
| chr7:148784752
|
A | G | 1 | a0001c0001t0001g0259 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1298+675A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784752 | ||||||
| chr7:148784881
|
A | G | 8 | a0001c0001t0001g0048a0001c0001t0001g0073a0001c0001t0001g0076others(5): Show | 8 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.1298+804A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784881 | ||||||
| chr7:148784890
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1298+813T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784890 | ||||||
| chr7:148785053
|
G | A | 11 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(8): Show | 11 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1298+976G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785053 | ||||||
| chr7:148785111
|
G | T | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1298+1034G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785111 | ||||||
| chr7:148785145
|
G | A | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1298+1068G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785145 | ||||||
| chr7:148785220
|
C | T | 14 | a0001c0001t0001g0091a0001c0001t0001g0108a0001c0001t0001g0109others(11): Show | 14 | HG00741.hp2 HG01243.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.1298+1143C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785220 | ||||||
| chr7:148785385
|
G | C | 10 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(7): Show | 10 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1299-1166G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785385 | ||||||
| chr7:148785517
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0122 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1299-1034C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785517 | ||||||
| chr7:148785523
|
A | AT | 20 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0042others(17): Show | 20 | HG00642.hp1 HG01123.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1299-1008dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr7 | 148785523 | |||||
| chr7:148785523
|
AT | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0020others(5): Show | 8 | HG01074.hp1 HG02523.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299-1008delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr7 | 148785523 | |||||
| chr7:148785855
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1299-696C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785855 | ||||||
| chr7:148786152
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG00423.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1299-399G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148786152 | ||||||
| chr7:148786170
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1299-381A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148786170 | ||||||
| chr7:148786320
|
G | C | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1299-231G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148786320 | ||||||
| chr7:148786508
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1299-43C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148786508 | ||||||
| chr7:148786661
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1347+62G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 12/21 | chr7 | 148786661 | ||||||
| chr7:148786668
|
G | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(230): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1347+69G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 12/21 | chr7 | 148786668 | ||||||
| chr7:148786927
|
A | G | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1348-62A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 12/21 | chr7 | 148786927 | ||||||
| chr7:148786974
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1348-15C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 12/21 | chr7 | 148786974 | ||||||
| chr7:148787189
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | HG02109.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1479+69G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787189 | ||||||
| chr7:148787290
|
A | C | 1 | a0001c0001t0004g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1479+170A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787290 | ||||||
| chr7:148787394
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1479+274A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787394 | ||||||
| chr7:148787507
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1479+387G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787507 | ||||||
| chr7:148787627
|
C | T | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1479+507C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787627 | ||||||
| chr7:148787646
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1479+526T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787646 | ||||||
| chr7:148787798
|
C | T | 16 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(13): Show | 16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1479+678C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787798 | ||||||
| chr7:148787805
|
C | G | 1 | a0001c0001t0001g0310 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1479+685C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787805 | ||||||
| chr7:148787886
|
G | A | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1480-671G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787886 | ||||||
| chr7:148787923
|
G | C | 1 | a0001c0001t0001g0234 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1480-634G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787923 | ||||||
| chr7:148787951
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1480-606G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787951 | ||||||
| chr7:148787952
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1480-605C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787952 | ||||||
| chr7:148788001
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1480-556G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788001 | ||||||
| chr7:148788042
|
T | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG00140.hp2 HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1480-515T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788042 | ||||||
| chr7:148788042
|
T | G | 1 | a0001c0002t0001g0286 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1480-515T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788042 | ||||||
| chr7:148788245
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1480-312G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788245 | ||||||
| chr7:148788345
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1480-212A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788345 | ||||||
| chr7:148788359
|
A | C | 1 | a0001c0001t0001g0246 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1480-198A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788359 | ||||||
| chr7:148788360
|
G | T | 1 | a0001c0001t0001g0246 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1480-197G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788360 | ||||||
| chr7:148788437
|
CTTTGCTA others(2): Show |
C | 3 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0244 | 3 | HG00738.hp2 HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1480-119_1480-111d others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788437 | ||||||
| chr7:148788511
|
G | A | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1480-46G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788511 | ||||||
| chr7:148788825
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1597+151C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148788825 | ||||||
| chr7:148788862
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1597+188C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148788862 | ||||||
| chr7:148788894
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1597+220G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148788894 | ||||||
| chr7:148789050
|
A | C | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1597+376A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148789050 | ||||||
| chr7:148789165
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1597+491A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148789165 | ||||||
| chr7:148789330
|
G | C | 34 | a0001c0001t0001g0147a0001c0001t0001g0155a0001c0001t0001g0160others(31): Show | 34 | HG00140.hp1 HG00639.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1598-420G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148789330 | ||||||
| chr7:148789357
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0310 | 2 | HG03239.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1598-393C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148789357 | ||||||
| chr7:148790023
|
C | T | 11 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(8): Show | 11 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1674+197C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790023 | ||||||
| chr7:148790038
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1674+212A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790038 | ||||||
| chr7:148790039
|
T | C | 7 | a0001c0001t0001g0082a0001c0001t0001g0104a0001c0001t0001g0105others(4): Show | 7 | HG02630.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1674+213T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790039 | ||||||
| chr7:148790090
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1675-220C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790090 | ||||||
| chr7:148790110
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1675-200A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790110 | ||||||
| chr7:148790237
|
G | T | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(233): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1675-73G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790237 | ||||||
| chr7:148790252
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1675-58C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790252 | ||||||
| chr7:148790303
|
T | C | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(220): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
splice_region_variant&intron_variant | LOW | c.1675-7T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790303 | ||||||
| chr7:148790745
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0003g0166 | 2 | HG01074.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1806+304G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148790745 | ||||||
| chr7:148790909
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1806+468A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148790909 | ||||||
| chr7:148791035
|
G | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0121 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1806+594G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791035 | ||||||
| chr7:148791152
|
C | G | 69 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0095others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1806+711C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791152 | ||||||
| chr7:148791207
|
A | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | NA19072.hp1 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1806+766A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791207 | ||||||
| chr7:148791415
|
C | T | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(231): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1806+974C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791415 | ||||||
| chr7:148791838
|
T | C | 79 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0086others(76): Show | 79 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1807-888T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791838 | ||||||
| chr7:148791872
|
C | T | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(231): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1807-854C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791872 | ||||||
| chr7:148791909
|
G | A | 3 | a0001c0003t0001g0116a0001c0003t0001g0123a0001c0003t0001g0264 | 3 | HG02145.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1807-817G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791909 | ||||||
| chr7:148791911
|
C | T | 69 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0095others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1807-815C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791911 | ||||||
| chr7:148791992
|
G | A | 6 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0098others(3): Show | 6 | HG01123.hp2 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1807-734G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791992 | ||||||
| chr7:148792046
|
T | C | 2 | a0001c0002t0001g0278a0001c0002t0001g0309 | 2 | NA18955.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1807-680T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792046 | ||||||
| chr7:148792052
|
G | T | 28 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0144others(25): Show | 28 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1807-674G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792052 | ||||||
| chr7:148792094
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1807-632G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792094 | ||||||
| chr7:148792117
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1807-609C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792117 | ||||||
| chr7:148792185
|
CA | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(223): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1807-526delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 148792185 | |||||
| chr7:148792301
|
G | T | 8 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1807-425G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792301 | ||||||
| chr7:148792678
|
A | C | 11 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130others(8): Show | 11 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1807-48A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792678 | ||||||
| chr7:148792682
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(3): Show | 6 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1807-44A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792682 | ||||||
| chr7:148793018
|
G | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1899+200G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793018 | ||||||
| chr7:148793135
|
G | A | 16 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(13): Show | 16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1899+317G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793135 | ||||||
| chr7:148793173
|
T | C | 4 | a0001c0002t0001g0278a0001c0002t0001g0284a0001c0002t0001g0286others(1): Show | 4 | HG00597.hp1 NA18955.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1899+355T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793173 | ||||||
| chr7:148793174
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1899+356G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793174 | ||||||
| chr7:148793218
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1899+400C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793218 | ||||||
| chr7:148793375
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1899+557C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793375 | ||||||
| chr7:148793742
|
A | C | 1 | a0001c0001t0001g0205 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1899+924A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793742 | ||||||
| chr7:148793791
|
A | G | 16 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(13): Show | 16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1899+973A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793791 | ||||||
| chr7:148793821
|
C | A | 16 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(13): Show | 16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1899+1003C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793821 | ||||||
| chr7:148793949
|
A | T | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1899+1131A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793949 | ||||||
| chr7:148793972
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1899+1154T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793972 | ||||||
| chr7:148794075
|
C | A | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1899+1257C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794075 | ||||||
| chr7:148794085
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0069 | 2 | HG01981.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1899+1267G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794085 | ||||||
| chr7:148794115
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1899+1297C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794115 | ||||||
| chr7:148794233
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1899+1415T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794233 | ||||||
| chr7:148794245
|
A | G | 5 | a0001c0001t0001g0124a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1899+1427A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794245 | ||||||
| chr7:148794266
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1899+1448T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794266 | ||||||
| chr7:148794496
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1899+1678G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794496 | ||||||
| chr7:148794917
|
C | T | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1899+2099C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794917 | ||||||
| chr7:148794980
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1899+2162C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794980 | ||||||
| chr7:148795082
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1899+2264C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795082 | ||||||
| chr7:148795123
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG02970.hp1 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1899+2305G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795123 | ||||||
| chr7:148795202
|
A | G | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1899+2384A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795202 | ||||||
| chr7:148795276
|
C | T | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1899+2458C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795276 | ||||||
| chr7:148795366
|
A | G | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1900-2446A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795366 | ||||||
| chr7:148795424
|
A | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0121 | 3 | HG02055.hp1 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1900-2388A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795424 | ||||||
| chr7:148795533
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1900-2279G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795533 | ||||||
| chr7:148795538
|
G | A | 15 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(12): Show | 15 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1900-2274G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795538 | ||||||
| chr7:148795595
|
T | G | 1 | a0001c0002t0001g0284 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1900-2217T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795595 | ||||||
| chr7:148795622
|
T | A | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1900-2190T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795622 | ||||||
| chr7:148795713
|
T | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1900-2099T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795713 | ||||||
| chr7:148795769
|
C | CA | 16 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0147others(13): Show | 16 | HG00735.hp1 HG02135.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1900-2024dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148795769 | |||||
| chr7:148795769
|
C | CAAAAAA | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(3): Show | 6 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1900-2029_1900-202 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148795769 | |||||
| chr7:148795769
|
CA | C | 9 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0111others(6): Show | 9 | HG01167.hp1 HG02723.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1900-2024delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148795769 | |||||
| chr7:148795799
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1900-2013A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795799 | ||||||
| chr7:148796018
|
T | TTGTGGTA others(14): Show |
20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1900-1789_1900-178 others(25): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148796018 | |||||
| chr7:148796024
|
C | T | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1900-1788C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796024 | ||||||
| chr7:148796032
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1900-1780A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796032 | ||||||
| chr7:148796199
|
A | G | 20 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(17): Show | 20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1900-1613A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796199 | ||||||
| chr7:148796220
|
A | G | 2 | a0001c0003t0001g0102a0001c0003t0001g0103 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1900-1592A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796220 | ||||||
| chr7:148796290
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1900-1522C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796290 | ||||||
| chr7:148796511
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(256): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1900-1301A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796511 | ||||||
| chr7:148796648
|
C | G | 1 | a0001c0001t0004g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1900-1164C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796648 | ||||||
| chr7:148796801
|
A | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG02257.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1900-1011A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796801 | ||||||
| chr7:148796952
|
T | C | 70 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0070others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.1900-860T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796952 | ||||||
| chr7:148797075
|
GT | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1900-734delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148797075 | |||||
| chr7:148797116
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1900-696G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797116 | ||||||
| chr7:148797146
|
A | T | 1 | a0001c0001t0004g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1900-666A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797146 | ||||||
| chr7:148797182
|
C | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0004g0120 | 3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1900-630C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797182 | ||||||
| chr7:148797188
|
A | G | 2 | a0001c0003t0001g0102a0001c0003t0001g0103 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1900-624A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797188 | ||||||
| chr7:148797258
|
C | T | 16 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(13): Show | 16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1900-554C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797258 | ||||||
| chr7:148797395
|
C | CA | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(131): Show | 136 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.1900-399dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148797395 | |||||
| chr7:148797395
|
C | CAA | 104 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1900-400_1900-399d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148797395 | |||||
| chr7:148797395
|
C | CAAA | 18 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(15): Show | 18 | HG00738.hp2 HG01175.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.1900-401_1900-399d others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148797395 | |||||
| chr7:148797414
|
T | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0064a0001c0001t0001g0240 | 3 | HG01167.hp1 HG03927.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1900-398T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797414 | ||||||
| chr7:148797424
|
G | A | 16 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(13): Show | 16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1900-388G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797424 | ||||||
| chr7:148797486
|
C | T | 11 | a0001c0001t0001g0035a0001c0001t0001g0113a0001c0001t0001g0129others(8): Show | 11 | HG01361.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1900-326C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797486 | ||||||
| chr7:148797525
|
G | A | 6 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(3): Show | 6 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1900-287G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797525 | ||||||
| chr7:148797550
|
A | G | 2 | a0001c0001t0001g0314a0001c0001t0001g0317 | 2 | HG01109.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1900-262A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797550 | ||||||
| chr7:148797653
|
T | G | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1900-159T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797653 | ||||||
| chr7:148797666
|
C | T | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(225): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1900-146C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797666 | ||||||
| chr7:148797702
|
AT | A | 69 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0033others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1900-93delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148797702 | |||||
| chr7:148797702
|
ATT | A | 23 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(20): Show | 23 | HG01123.hp2 HG02145.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1900-94_1900-93del others(2): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148797702 | |||||
| chr7:148798048
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2030+29C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 19/21 | chr7 | 148798048 | ||||||
| chr7:148798176
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2030+157C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 19/21 | chr7 | 148798176 | ||||||
| chr7:148798398
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2031-174C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 19/21 | chr7 | 148798398 | ||||||
| chr7:148798434
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2031-138C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 19/21 | chr7 | 148798434 | ||||||
| chr7:148798548
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2031-24C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 19/21 | chr7 | 148798548 | ||||||
| chr7:148798733
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2136+56G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 20/21 | chr7 | 148798733 | ||||||
| chr7:148798740
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2136+63C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 20/21 | chr7 | 148798740 | ||||||
| chr7:148798768
|
A | G | 11 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(8): Show | 11 | HG00738.hp2 HG01175.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2136+91A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 20/21 | chr7 | 148798768 | ||||||
| chr7:148798914
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2136+237T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 20/21 | chr7 | 148798914 | ||||||
| chr7:148799184
|
G | A | 16 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(13): Show | 16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2137-91G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 20/21 | chr7 | 148799184 | ||||||
| chr7:148799186
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2137-89C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 20/21 | chr7 | 148799186 | ||||||
| chr7:148799559
|
A | C | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2250+171A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148799559 | ||||||
| chr7:148799691
|
A | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(4): Show | 7 | HG01433.hp2 HG01952.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2250+303A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148799691 | ||||||
| chr7:148799733
|
T | G | 4 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2250+345T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148799733 | ||||||
| chr7:148799824
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(3): Show | 6 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2250+436G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148799824 | ||||||
| chr7:148799833
|
C | T | 4 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2250+445C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148799833 | ||||||
| chr7:148799867
|
T | C | 21 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(18): Show | 21 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2250+479T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148799867 | ||||||
| chr7:148800068
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2251-434C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800068 | ||||||
| chr7:148800069
|
A | G | 4 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2251-433A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800069 | ||||||
| chr7:148800137
|
A | G | 6 | a0001c0001t0001g0124a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2251-365A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800137 | ||||||
| chr7:148800241
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2251-261G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800241 | ||||||
| chr7:148800296
|
C | T | 14 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(11): Show | 14 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2251-206C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800296 | ||||||
| chr7:148800359
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2251-143A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800359 | ||||||
| chr7:148800371
|
C | T | 14 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(11): Show | 14 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2251-131C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800371 | ||||||
| chr7:148800397
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2251-105C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800397 | ||||||
| chr7:148800417
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2251-85G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800417 |