| geneid | 27098 |
|---|---|
| ensemblid | ENSG00000079101.18 |
| hgncid | 2096 |
| symbol | CLUL1 |
| name | clusterin like 1 |
| refseq_nuc | NM_001393344.1 |
| refseq_prot | NP_001380273.1 |
| ensembl_nuc | ENST00000692774.1 |
| ensembl_prot | ENSP00000510271.1 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 596988 |
| end | 650182 |
| strand | + |
| ver | v1.2 |
| region | chr18:596988-650182 |
| region5000 | chr18:591988-655182 |
| regionname0 | CLUL1_chr18_596988_650182 |
| regionname5000 | CLUL1_chr18_591988_655182 |
| 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 | 466 | 405 | 89 | 78 | 170 | 18 | 48 | 127 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0002 | 0/0 | 466 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0003 | 0/0 | 466 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0004 | 0/0 | 466 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0005 | 0/0 | 466 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0006 | 0/0 | 466 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0007 | 0/0 | 466 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| 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 | 1401 | 397 | 83 | 77 | 170 | 18 | 47 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| c0002 | 0/0 | 1401 | 3 | 3 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| c0003 | 0/0 | 1401 | 2 | 2 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| c0004 | 0/0 | 1401 | 2 | 1 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| c0005 | 0/0 | 1401 | 2 | 2 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| c0006 | 0/0 | 1401 | 2 | 2 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| c0007 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| c0008 | 0/0 | 1401 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| c0009 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| c0010 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| c0011 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| c0012 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| 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 | 559 | 278 | 44 | 59 | 131 | 12 | 30 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| t0002 | 0/0 | 554 | 70 | 8 | 9 | 37 | 1 | 15 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| t0003 | 0/0 | 554 | 29 | 24 | 5 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| t0004 | 0/0 | 559 | 23 | 16 | 4 | 0 | 2 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| t0005 | 0/0 | 559 | 5 | 0 | 0 | 3 | 2 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| t0006 | 0/0 | 554 | 4 | 4 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| t0007 | 0/0 | 559 | 2 | 0 | 0 | 0 | 0 | 2 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| t0008 | 0/0 | 554 | 2 | 0 | 1 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| t0009 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| 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 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0260 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0378 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0384 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0394 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0396 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0400 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0401 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0402 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0403 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0406 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0407 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| 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 | 1401 | 397 | 83 | 77 | 170 | 18 | 47 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0002 | 0/0 | 1401 | 3 | 3 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0004 | 0/0 | 1401 | 2 | 1 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0008 | 0/0 | 1401 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0011 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0012 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0002c0005 | 0/0 | 1401 | 2 | 2 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0003c0006 | 0/0 | 1401 | 2 | 2 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0004c0003 | 0/0 | 1401 | 2 | 2 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0005c0010 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0006c0009 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0007c0007 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1959 | 267 | 34 | 59 | 131 | 12 | 29 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0001t0002 | 0/0 | 1954 | 67 | 7 | 9 | 35 | 1 | 15 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0001t0003 | 0/0 | 1954 | 27 | 23 | 4 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0001t0004 | 0/0 | 1959 | 22 | 15 | 4 | 0 | 2 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0001t0005 | 0/0 | 1959 | 5 | 0 | 0 | 3 | 2 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0001t0006 | 0/0 | 1954 | 4 | 4 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0001t0007 | 0/0 | 1959 | 2 | 0 | 0 | 0 | 0 | 2 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0001t0008 | 0/0 | 1954 | 2 | 0 | 1 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0001t0009 | 0/0 | 1959 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0002t0001 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0002t0003 | 0/0 | 1954 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0004t0001 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0004t0003 | 0/0 | 1954 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0008t0001 | 0/0 | 1959 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0011t0001 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0001c0012t0001 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0002c0005t0001 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0003c0006t0002 | 0/0 | 1954 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0003c0006t0004 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0004c0003t0001 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0005c0010t0002 | 0/0 | 1954 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0006c0009t0002 | 0/0 | 1954 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| a0007c0007t0001 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | copy fasta | chr18 | 591988 | 655182 |
| 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 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0260 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0394 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0396 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0400 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0401 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0402 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0403 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0406 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0407 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0001g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0004g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0005g0378 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0005g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0008g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0001t0009g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0004t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0004t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0008t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0011t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0001c0012t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0002c0005t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0002c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0003c0006t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0003c0006t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0004c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0004c0003t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0005c0010t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0006c0009t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| a0007c0007t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | GBR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | GBR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0401 | EUR | GBR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00140 | hp2 | a0001 | c0001 | t0008 | g0023 | EUR | GBR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0053 | EUR | FIN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0407 | EUR | FIN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0060 | EUR | FIN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0406 | EAS | CHS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0055 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0380 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0382 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0386 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0341 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01168 | hp1 | a0001 | c0001 | t0008 | g0024 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0377 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01192 | hp1 | a0001 | c0004 | t0003 | g0344 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0367 | AMR | PUR | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0062 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0376 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0383 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0352 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0369 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0400 | EUR | IBS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0379 | EUR | IBS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0378 | EUR | IBS | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0371 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02055 | hp1 | a0004 | c0003 | t0001 | g0075 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0381 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02135 | hp1 | a0005 | c0010 | t0002 | g0018 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CDX | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | CDX | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0408 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0404 | EAS | KHV | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0402 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0351 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02615 | hp1 | a0003 | c0006 | t0004 | g0317 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02615 | hp2 | a0007 | c0007 | t0001 | g0282 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02622 | hp1 | a0003 | c0006 | t0002 | g0127 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0389 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02647 | hp2 | a0004 | c0003 | t0001 | g0366 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0374 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0385 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0372 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0121 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0340 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0333 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02738 | hp1 | a0001 | c0008 | t0001 | g0350 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0365 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0281 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02895 | hp1 | a0002 | c0005 | t0001 | g0048 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0343 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0140 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0105 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0368 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0396 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0370 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0316 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0314 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0310 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0345 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0342 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03225 | hp1 | a0001 | c0011 | t0001 | g0071 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0059 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0335 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03490 | hp2 | a0001 | c0001 | t0007 | g0056 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0334 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0270 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | ESN | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0261 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0388 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0347 | SAS | STU | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | STU | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0373 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0403 | SAS | PJL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0375 | SAS | BEB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0364 | SAS | BEB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0339 | SAS | STU | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0318 | SAS | BEB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0336 | SAS | STU | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | STU | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0338 | SAS | STU | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0311 | AFR | YRI | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | YRI | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CHB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CHB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | YRI | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18939 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0399 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0392 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18968 | hp2 | a0006 | c0009 | t0002 | g0015 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0393 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0390 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19010 | hp1 | a0001 | c0001 | t0009 | g0218 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0322 | AFR | LWK | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19030 | hp2 | a0001 | c0012 | t0001 | g0257 | AFR | LWK | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | LWK | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0398 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0409 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0391 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0395 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0397 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0387 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0346 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | YRI | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | YRI | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ASW | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | ASW | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0394 | EUR | TSI | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | TSI | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0384 | EUR | TSI | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0057 | SAS | GIH | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0324 | SAS | GIH | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02109 | hp1 | a0002 | c0005 | t0001 | g0125 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0264 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0312 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0405 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0262 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | MSL | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | USA | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | USA | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | USA | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | USA | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | LWK | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0315 | AFR | LWK | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0296 | REF | REF | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0260 | REF | REF | CLUL1_chr18_591988_655182 | CLUL1 | chr18 | 591988 | 655182 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:627190
|
G | A | 1 | a0007 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.517G>A | p.Glu173Lys | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/10 | 794/1959 | 517/1401 | 173/466 | chr18 | 627190 | ||
| chr18:633346
|
G | C | 1 | a0004 | 2 | HG02055.hp1 HG02647.hp2 |
missense_variant | MODERATE | c.905G>C | p.Arg302Thr | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/10 | 1182/1959 | 905/1401 | 302/466 | chr18 | 633346 | ||
| chr18:633347
|
A | T | 2 | a0003a0004 | 4 | HG02055.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
missense_variant | MODERATE | c.906A>T | p.Arg302Ser | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/10 | 1183/1959 | 906/1401 | 302/466 | chr18 | 633347 | ||
| chr18:641363
|
A | G | 1 | a0002 | 2 | HG02109.hp1 HG02895.hp1 |
missense_variant | MODERATE | c.1031A>G | p.Asp344Gly | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/10 | 1308/1959 | 1031/1401 | 344/466 | chr18 | 641363 | ||
| chr18:641537
|
T | C | 1 | a0006 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.1205T>C | p.Ile402Thr | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/10 | 1482/1959 | 1205/1401 | 402/466 | chr18 | 641537 | ||
| chr18:644963
|
G | A | 1 | a0005 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.1263G>A | p.Met421Ile | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/10 | 1540/1959 | 1263/1401 | 421/466 | chr18 | 644963 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:618036
|
G | A | 1 | a0001c0002 | 3 | HG02922.hp1 HG02976.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.36G>A | p.Leu12Leu | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/10 | 313/1959 | 36/1401 | 12/466 | chr18 | 618036 | ||
| chr18:633380
|
A | G | 1 | a0001c0012 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.939A>G | p.Ser313Ser | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/10 | 1216/1959 | 939/1401 | 313/466 | chr18 | 633380 | ||
| chr18:633419
|
G | A | 1 | a0001c0008 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.978G>A | p.Gln326Gln | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/10 | 1255/1959 | 978/1401 | 326/466 | chr18 | 633419 | ||
| chr18:641364
|
C | T | 1 | a0001c0011 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.1032C>T | p.Asp344Asp | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/10 | 1309/1959 | 1032/1401 | 344/466 | chr18 | 641364 | ||
| chr18:641454
|
G | C | 1 | a0001c0004 | 2 | HG01192.hp1 HG02809.hp2 |
synonymous_variant | LOW | c.1122G>C | p.Leu374Leu | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/10 | 1399/1959 | 1122/1401 | 374/466 | chr18 | 641454 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:596992
|
T | G | 1 | a0001c0001t0005 | 5 | HG01516.hp2 HG01517.hp2 NA18939.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-273T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/10 | 21009 | chr18 | 596992 | |||||
| chr18:596995
|
G | A | 1 | a0001c0001t0006 | 4 | HG02109.hp2 HG02559.hp1 HG02717.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-270G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/10 | 21006 | chr18 | 596995 | |||||
| chr18:597003
|
C | G | 1 | a0001c0001t0007 | 2 | HG03490.hp2 NA20905.hp1 |
5_prime_UTR_variant | MODIFIER | c.-262C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/10 | 20998 | chr18 | 597003 | |||||
| chr18:606993
|
G | A | 1 | a0001c0001t0008 | 2 | HG00140.hp2 HG01168.hp1 |
5_prime_UTR_variant | MODIFIER | c.-120G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/10 | 11008 | chr18 | 606993 | |||||
| chr18:606993
|
G | T | 5 | a0001c0001t0003a0001c0001t0004a0001c0002t0003others(2): Show | 52 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(49): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-120G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/10 | chr18 | 606993 | ||||||
| chr18:607008
|
G | T | 1 | a0001c0001t0009 | 1 | NA19010.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/10 | 10993 | chr18 | 607008 | |||||
| chr18:607024
|
A | T | 5 | a0001c0001t0003a0001c0001t0004a0001c0002t0003others(2): Show | 52 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-89A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/10 | 10977 | chr18 | 607024 | |||||
| chr18:607068
|
T | C | 5 | a0001c0001t0003a0001c0001t0004a0001c0002t0003others(2): Show | 52 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-45T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/10 | 10933 | chr18 | 607068 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:597146
|
G | A | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(38): Show | 41 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-136+17G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 597146 | ||||||
| chr18:597270
|
C | T | 65 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0349others(62): Show | 67 | HG00140.hp1 HG00280.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.-136+141C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 597270 | ||||||
| chr18:597273
|
T | G | 4 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 4 | HG01891.hp1 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136+144T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 597273 | ||||||
| chr18:597323
|
CA | C | 63 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.-136+198delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 597323 | |||||
| chr18:597401
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-136+272G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 597401 | ||||||
| chr18:597579
|
A | G | 8 | a0001c0001t0003g0313a0001c0001t0004g0310a0001c0001t0004g0311others(5): Show | 8 | HG02486.hp1 HG02615.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136+450A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 597579 | ||||||
| chr18:597687
|
A | G | 5 | a0001c0001t0003g0313a0001c0001t0004g0314a0001c0001t0004g0315others(2): Show | 5 | HG02615.hp1 HG03098.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136+558A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 597687 | ||||||
| chr18:597751
|
T | G | 54 | a0001c0001t0001g0052a0001c0001t0001g0065a0001c0001t0001g0066others(51): Show | 54 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.-136+622T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 597751 | ||||||
| chr18:597854
|
T | C | 12 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(9): Show | 12 | HG01070.hp2 HG01081.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-136+725T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 597854 | ||||||
| chr18:597950
|
C | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0292others(18): Show | 23 | HG00639.hp1 HG00639.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.-136+821C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 597950 | ||||||
| chr18:597967
|
G | C | 7 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0109others(4): Show | 7 | HG01361.hp1 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136+838G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 597967 | ||||||
| chr18:598037
|
A | T | 1 | a0001c0001t0002g0291 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-136+908A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 598037 | ||||||
| chr18:598162
|
T | C | 1 | a0001c0001t0002g0320 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-136+1033T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 598162 | ||||||
| chr18:598169
|
G | A | 25 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0050others(22): Show | 25 | HG00609.hp2 HG00733.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-136+1040G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 598169 | ||||||
| chr18:598340
|
T | G | 23 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(20): Show | 23 | HG00738.hp2 HG01167.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.-136+1211T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 598340 | ||||||
| chr18:598416
|
G | C | 120 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-136+1287G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 598416 | ||||||
| chr18:598481
|
C | T | 2 | a0001c0001t0004g0310a0001c0001t0004g0311 | 2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-136+1352C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 598481 | ||||||
| chr18:598725
|
A | G | 1 | a0001c0001t0001g0409 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-136+1596A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 598725 | ||||||
| chr18:598855
|
A | G | 1 | a0001c0001t0003g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-136+1726A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 598855 | ||||||
| chr18:599052
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-136+1923A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599052 | ||||||
| chr18:599388
|
T | A | 12 | a0001c0001t0002g0100a0001c0001t0003g0113a0001c0001t0003g0114others(9): Show | 12 | HG01106.hp1 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.-136+2259T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599388 | ||||||
| chr18:599405
|
G | T | 124 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-136+2276G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599405 | ||||||
| chr18:599590
|
G | C | 2 | a0001c0001t0002g0063a0001c0001t0002g0064 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-136+2461G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599590 | ||||||
| chr18:599618
|
C | T | 35 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(32): Show | 35 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-136+2489C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599618 | ||||||
| chr18:599641
|
A | C | 23 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0103others(20): Show | 23 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.-136+2512A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599641 | ||||||
| chr18:599654
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-136+2525C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599654 | ||||||
| chr18:599670
|
C | T | 5 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0109others(2): Show | 5 | HG01361.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+2541C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599670 | ||||||
| chr18:599675
|
G | C | 72 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-136+2546G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599675 | ||||||
| chr18:599729
|
G | C | 12 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(9): Show | 12 | HG00738.hp2 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-136+2600G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599729 | ||||||
| chr18:599769
|
A | G | 12 | a0001c0001t0002g0100a0001c0001t0003g0113a0001c0001t0003g0114others(9): Show | 12 | HG01106.hp1 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.-136+2640A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599769 | ||||||
| chr18:599809
|
GTAGTCCC others(9): Show |
G | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0354 | 3 | NA18962.hp2 NA18980.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-136+2697_-136+271 others(20): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 599809 | |||||
| chr18:599824
|
C | G | 1 | a0001c0001t0001g0286 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-136+2695C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599824 | ||||||
| chr18:599856
|
G | A | 1 | a0001c0001t0002g0321 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-136+2727G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599856 | ||||||
| chr18:599873
|
G | A | 14 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0103others(11): Show | 14 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.-136+2744G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 599873 | ||||||
| chr18:599947
|
C | CA | 10 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0109others(7): Show | 10 | HG01361.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-136+2833dupA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 599947 | |||||
| chr18:599947
|
C | CAA | 76 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-136+2832_-136+283 others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 599947 | |||||
| chr18:599947
|
C | CAAA | 18 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0002g0101others(15): Show | 18 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.-136+2831_-136+283 others(7): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 599947 | |||||
| chr18:599947
|
CA | C | 9 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0123others(6): Show | 9 | HG00738.hp2 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-136+2833delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 599947 | |||||
| chr18:600017
|
T | A | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-136+2888T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 600017 | ||||||
| chr18:600198
|
CT | C | 21 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0103others(18): Show | 21 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-136+3076delT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 600198 | |||||
| chr18:600281
|
A | G | 1 | a0001c0001t0003g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-136+3152A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 600281 | ||||||
| chr18:600441
|
C | T | 106 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-136+3312C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 600441 | ||||||
| chr18:600541
|
CT | C | 106 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-136+3414delT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 600541 | |||||
| chr18:600668
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-136+3539T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 600668 | ||||||
| chr18:600998
|
G | A | 6 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(3): Show | 6 | HG02080.hp1 HG02135.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+3869G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 600998 | ||||||
| chr18:601087
|
C | G | 96 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-136+3958C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 601087 | ||||||
| chr18:601128
|
C | T | 7 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280others(4): Show | 7 | HG02615.hp2 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+3999C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 601128 | ||||||
| chr18:601375
|
G | A | 26 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0050others(23): Show | 26 | HG00609.hp2 HG00733.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.-136+4246G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 601375 | ||||||
| chr18:601515
|
A | T | 125 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-136+4386A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 601515 | ||||||
| chr18:601561
|
T | C | 9 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0109others(6): Show | 9 | HG01361.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-136+4432T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 601561 | ||||||
| chr18:601612
|
A | G | 7 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(4): Show | 7 | HG00738.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136+4483A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 601612 | ||||||
| chr18:601645
|
C | CA | 82 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-136+4530dupA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 601645 | |||||
| chr18:601645
|
C | CAA | 18 | a0001c0001t0001g0047a0001c0001t0002g0101a0001c0001t0002g0102others(15): Show | 18 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-136+4529_-136+453 others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 601645 | |||||
| chr18:601645
|
CA | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0072others(40): Show | 44 | HG00323.hp2 HG00423.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.-136+4530delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 601645 | |||||
| chr18:601676
|
G | A | 2 | a0001c0001t0001g0072a0001c0011t0001g0071 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-136+4547G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 601676 | ||||||
| chr18:601795
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-136+4666C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 601795 | ||||||
| chr18:601947
|
G | A | 12 | a0001c0001t0002g0100a0001c0001t0003g0113a0001c0001t0003g0114others(9): Show | 12 | HG01106.hp1 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.-136+4818G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 601947 | ||||||
| chr18:602081
|
G | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(218): Show | 225 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.-135-4897G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602081 | ||||||
| chr18:602150
|
C | T | 2 | a0001c0001t0004g0058a0001c0001t0004g0059 | 2 | HG01069.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-135-4828C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602150 | ||||||
| chr18:602222
|
G | T | 26 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0050others(23): Show | 26 | HG00609.hp2 HG00733.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.-135-4756G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602222 | ||||||
| chr18:602346
|
C | G | 1 | a0001c0001t0002g0258 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-135-4632C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602346 | ||||||
| chr18:602367
|
G | C | 2 | a0001c0001t0003g0113a0001c0001t0003g0313 | 2 | HG01884.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-4611G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602367 | ||||||
| chr18:602431
|
T | C | 6 | a0001c0001t0004g0310a0001c0001t0004g0311a0001c0001t0004g0314others(3): Show | 6 | HG02615.hp1 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-4547T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602431 | ||||||
| chr18:602432
|
C | T | 1 | a0001c0001t0001g0405 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-135-4546C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602432 | ||||||
| chr18:602440
|
C | T | 2 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-135-4538C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602440 | ||||||
| chr18:602456
|
G | A | 1 | a0001c0001t0003g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-135-4522G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602456 | ||||||
| chr18:602505
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-135-4473G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602505 | ||||||
| chr18:602739
|
G | A | 1 | a0001c0001t0004g0408 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-135-4239G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602739 | ||||||
| chr18:602960
|
C | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(4): Show | 7 | HG00738.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-4018C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602960 | ||||||
| chr18:602973
|
G | A | 3 | a0001c0001t0003g0340a0001c0001t0003g0341a0001c0001t0003g0342 | 3 | HG01167.hp1 HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-135-4005G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 602973 | ||||||
| chr18:603211
|
C | A | 9 | a0001c0001t0001g0355a0001c0001t0001g0356a0001c0001t0001g0357others(6): Show | 9 | NA18963.hp1 NA18964.hp1 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.-135-3767C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603211 | ||||||
| chr18:603266
|
T | G | 11 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0115others(8): Show | 11 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-135-3712T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603266 | ||||||
| chr18:603311
|
T | C | 2 | a0001c0001t0004g0053a0001c0001t0004g0408 | 2 | HG00280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-135-3667T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603311 | ||||||
| chr18:603391
|
G | C | 36 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(33): Show | 36 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.-135-3587G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603391 | ||||||
| chr18:603400
|
TGAG | T | 3 | a0001c0001t0004g0060a0001c0001t0004g0061a0001c0001t0004g0062 | 3 | HG00323.hp1 HG01255.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-135-3574_-135-357 others(7): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 603400 | |||||
| chr18:603438
|
G | A | 74 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.-135-3540G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603438 | ||||||
| chr18:603467
|
A | AT | 13 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(10): Show | 13 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-135-3503dupT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 603467 | |||||
| chr18:603489
|
A | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | NA18953.hp1 NA18966.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-135-3489A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603489 | ||||||
| chr18:603588
|
G | A | 36 | a0001c0001t0002g0347a0001c0001t0003g0011a0001c0001t0003g0012others(33): Show | 36 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.-135-3390G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603588 | ||||||
| chr18:603600
|
G | A | 126 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-135-3378G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603600 | ||||||
| chr18:603601
|
T | C | 1 | a0001c0001t0006g0121 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-135-3377T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603601 | ||||||
| chr18:603733
|
C | A | 26 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0050others(23): Show | 26 | HG00140.hp2 HG00609.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-135-3245C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603733 | ||||||
| chr18:603737
|
T | G | 1 | a0001c0001t0001g0145 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-135-3241T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603737 | ||||||
| chr18:603760
|
C | T | 3 | a0001c0001t0001g0283a0001c0001t0001g0284a0007c0007t0001g0282 | 3 | HG02615.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-135-3218C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603760 | ||||||
| chr18:603776
|
C | T | 1 | a0001c0012t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-135-3202C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603776 | ||||||
| chr18:603782
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-135-3196C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603782 | ||||||
| chr18:603843
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02055.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-3135G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603843 | ||||||
| chr18:603871
|
G | A | 126 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-135-3107G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603871 | ||||||
| chr18:603930
|
G | A | 1 | a0001c0001t0002g0318 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-135-3048G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 603930 | ||||||
| chr18:604025
|
C | G | 4 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(1): Show | 4 | HG02615.hp1 HG03098.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-2953C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 604025 | ||||||
| chr18:604373
|
G | C | 395 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(392): Show | 400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.-135-2605G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 604373 | ||||||
| chr18:604795
|
G | T | 1 | a0001c0001t0002g0112 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-135-2183G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 604795 | ||||||
| chr18:604818
|
G | T | 4 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(1): Show | 4 | HG02615.hp1 HG03098.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-2160G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 604818 | ||||||
| chr18:604995
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0072others(46): Show | 50 | HG00323.hp2 HG00423.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.-135-1983G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 604995 | ||||||
| chr18:605312
|
G | A | 76 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-135-1666G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 605312 | ||||||
| chr18:605342
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-135-1636A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 605342 | ||||||
| chr18:605361
|
C | T | 1 | a0002c0005t0001g0125 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-135-1617C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 605361 | ||||||
| chr18:605487
|
G | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0072others(49): Show | 53 | HG00323.hp2 HG00423.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.-135-1491G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 605487 | ||||||
| chr18:605530
|
G | A | 46 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(43): Show | 46 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.-135-1448G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 605530 | ||||||
| chr18:605681
|
T | C | 2 | a0001c0001t0004g0310a0001c0001t0004g0311 | 2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-135-1297T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 605681 | ||||||
| chr18:605710
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-135-1268G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 605710 | ||||||
| chr18:605716
|
A | T | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-135-1262A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 605716 | ||||||
| chr18:605825
|
C | T | 14 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(11): Show | 14 | HG02071.hp2 HG02132.hp2 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.-135-1153C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 605825 | ||||||
| chr18:605864
|
T | C | 1 | a0001c0001t0006g0121 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-135-1114T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 605864 | ||||||
| chr18:605876
|
A | G | 2 | a0001c0001t0004g0310a0001c0001t0004g0311 | 2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-135-1102A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 605876 | ||||||
| chr18:605970
|
G | A | 51 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.-135-1008G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 605970 | ||||||
| chr18:606115
|
A | T | 137 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-135-863A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 606115 | ||||||
| chr18:606227
|
A | C | 3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0002g0041 | 3 | NA18984.hp2 NA18986.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-135-751A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 606227 | ||||||
| chr18:606330
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(1): Show | 4 | NA18944.hp2 NA18948.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-648G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 606330 | ||||||
| chr18:606336
|
C | T | 2 | a0001c0001t0004g0310a0001c0001t0004g0311 | 2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-135-642C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 606336 | ||||||
| chr18:606495
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0006g0121 | 2 | HG00621.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-135-483G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 606495 | ||||||
| chr18:606715
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-135-263G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 1/9 | chr18 | 606715 | ||||||
| chr18:607190
|
C | T | 1 | a0001c0001t0002g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-14+91C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 607190 | ||||||
| chr18:607210
|
T | C | 52 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.-14+111T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 607210 | ||||||
| chr18:607238
|
T | C | 52 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.-14+139T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 607238 | ||||||
| chr18:607376
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-14+277G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 607376 | ||||||
| chr18:607503
|
G | T | 1 | a0001c0001t0001g0276 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-14+404G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 607503 | ||||||
| chr18:607513
|
G | A | 52 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.-14+414G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 607513 | ||||||
| chr18:607616
|
C | T | 5 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+517C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 607616 | ||||||
| chr18:607682
|
C | T | 1 | a0001c0002t0003g0105 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-14+583C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 607682 | ||||||
| chr18:608018
|
G | A | 52 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.-14+919G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608018 | ||||||
| chr18:608070
|
C | T | 5 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0109others(2): Show | 5 | HG01361.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+971C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608070 | ||||||
| chr18:608178
|
C | T | 1 | a0001c0001t0003g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14+1079C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608178 | ||||||
| chr18:608179
|
C | G | 41 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(38): Show | 41 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.-14+1080C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608179 | ||||||
| chr18:608312
|
C | T | 87 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-14+1213C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608312 | ||||||
| chr18:608342
|
A | G | 45 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0050others(42): Show | 45 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-14+1243A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608342 | ||||||
| chr18:608416
|
T | A | 75 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.-14+1317T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608416 | ||||||
| chr18:608455
|
C | CT | 52 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.-14+1358dupT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 608455 | |||||
| chr18:608468
|
A | C | 52 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.-14+1369A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608468 | ||||||
| chr18:608480
|
A | G | 4 | a0001c0001t0001g0400a0001c0001t0001g0401a0001c0001t0001g0402others(1): Show | 4 | HG00140.hp1 HG01515.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+1381A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608480 | ||||||
| chr18:608498
|
TTAAAA | T | 4 | a0001c0001t0001g0122a0001c0001t0002g0006a0001c0001t0002g0007others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+1400_-14+1404d others(7): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608498 | ||||||
| chr18:608500
|
AAAAC | A | 41 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(38): Show | 41 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.-14+1420_-14+1423d others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 608500 | |||||
| chr18:608683
|
A | C | 1 | a0001c0001t0003g0322 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-14+1584A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608683 | ||||||
| chr18:608718
|
T | TAAAC | 14 | a0001c0001t0003g0104a0001c0001t0003g0117a0001c0001t0003g0118others(11): Show | 14 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14+1635_-14+1638d others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 608718 | |||||
| chr18:608762
|
C | A | 11 | a0001c0001t0003g0139a0001c0001t0004g0136a0001c0001t0004g0137others(8): Show | 11 | HG02280.hp1 HG02486.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-14+1663C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608762 | ||||||
| chr18:608787
|
G | T | 3 | a0001c0001t0003g0340a0001c0001t0003g0341a0001c0001t0003g0342 | 3 | HG01167.hp1 HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-14+1688G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608787 | ||||||
| chr18:608958
|
G | A | 3 | a0001c0001t0002g0126a0001c0001t0002g0128a0003c0006t0002g0127 | 3 | HG02622.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-14+1859G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 608958 | ||||||
| chr18:609139
|
G | A | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-14+2040G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 609139 | ||||||
| chr18:609201
|
T | C | 1 | a0001c0001t0004g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-14+2102T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 609201 | ||||||
| chr18:609371
|
A | G | 3 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241 | 3 | NA18983.hp2 NA18984.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-14+2272A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 609371 | ||||||
| chr18:609707
|
C | G | 15 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(12): Show | 15 | HG01167.hp1 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-14+2608C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 609707 | ||||||
| chr18:609717
|
G | A | 19 | a0001c0001t0001g0278a0001c0001t0002g0006a0001c0001t0002g0007others(16): Show | 19 | HG01167.hp1 HG01192.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14+2618G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 609717 | ||||||
| chr18:609724
|
C | T | 7 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+2625C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 609724 | ||||||
| chr18:609740
|
C | T | 1 | a0001c0012t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-14+2641C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 609740 | ||||||
| chr18:609823
|
CA | C | 172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0042others(169): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-14+2744delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 609823 | |||||
| chr18:609823
|
CAA | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 211 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.-14+2743_-14+2744d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 609823 | |||||
| chr18:609897
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-14+2798C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 609897 | ||||||
| chr18:609911
|
C | T | 3 | a0001c0001t0004g0310a0001c0001t0004g0311a0001c0001t0006g0121 | 3 | HG02717.hp2 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-14+2812C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 609911 | ||||||
| chr18:609953
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-14+2854C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 609953 | ||||||
| chr18:609954
|
A | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0049others(228): Show | 233 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-14+2855A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 609954 | ||||||
| chr18:610051
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-14+2952T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610051 | ||||||
| chr18:610085
|
T | C | 1 | a0001c0001t0001g0388 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-14+2986T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610085 | ||||||
| chr18:610085
|
T | TATC | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(109): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.-14+2988_-14+2990d others(5): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 610085 | |||||
| chr18:610112
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-14+3013T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610112 | ||||||
| chr18:610157
|
A | G | 341 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(338): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.-14+3058A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610157 | ||||||
| chr18:610175
|
C | T | 1 | a0005c0010t0002g0018 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-14+3076C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610175 | ||||||
| chr18:610199
|
A | T | 355 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(352): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-14+3100A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610199 | ||||||
| chr18:610235
|
G | A | 6 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(3): Show | 6 | NA18954.hp2 NA18975.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14+3136G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610235 | ||||||
| chr18:610273
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-14+3174G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610273 | ||||||
| chr18:610305
|
T | C | 8 | a0001c0001t0001g0049a0001c0001t0001g0389a0001c0001t0003g0012others(5): Show | 8 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14+3206T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610305 | ||||||
| chr18:610382
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(299): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-14+3283A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610382 | ||||||
| chr18:610449
|
T | TG | 20 | a0001c0001t0001g0052a0001c0001t0001g0131a0001c0001t0001g0135others(17): Show | 20 | HG00280.hp2 HG00733.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14+3350_-14+3351i others(3): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610449 | ||||||
| chr18:610519
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-14+3420C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610519 | ||||||
| chr18:610531
|
G | A | 4 | a0001c0001t0002g0031a0001c0001t0004g0060a0001c0001t0004g0061others(1): Show | 4 | HG00099.hp2 HG00323.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+3432G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610531 | ||||||
| chr18:610565
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-14+3466C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610565 | ||||||
| chr18:610566
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-14+3467G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610566 | ||||||
| chr18:610618
|
G | T | 2 | a0001c0001t0004g0138a0001c0001t0004g0140 | 2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-14+3519G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610618 | ||||||
| chr18:610634
|
C | T | 4 | a0001c0001t0001g0124a0001c0001t0003g0108a0001c0001t0003g0342others(1): Show | 4 | HG00738.hp2 HG02615.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+3535C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610634 | ||||||
| chr18:610675
|
G | A | 3 | a0001c0001t0001g0124a0001c0001t0003g0108a0003c0006t0004g0317 | 3 | HG00738.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-14+3576G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610675 | ||||||
| chr18:610713
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0295a0001c0001t0001g0352others(2): Show | 6 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+3614G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610713 | ||||||
| chr18:610736
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-14+3637G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610736 | ||||||
| chr18:610774
|
C | T | 2 | a0001c0001t0004g0138a0001c0001t0004g0140 | 2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-14+3675C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610774 | ||||||
| chr18:610898
|
A | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0307others(12): Show | 16 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.-14+3799A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 610898 | ||||||
| chr18:611024
|
C | T | 1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-14+3925C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611024 | ||||||
| chr18:611061
|
A | G | 403 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(400): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.-14+3962A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611061 | ||||||
| chr18:611199
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-14+4100A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611199 | ||||||
| chr18:611234
|
C | CT | 32 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0073others(29): Show | 33 | HG00323.hp2 HG00741.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.-14+4153dupT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 611234 | |||||
| chr18:611234
|
CT | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-14+4153delT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 611234 | |||||
| chr18:611234
|
CTT | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0049others(84): Show | 89 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.-14+4152_-14+4153d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 611234 | |||||
| chr18:611234
|
CTTT | C | 7 | a0001c0001t0001g0296a0001c0001t0003g0012a0001c0001t0003g0013others(4): Show | 7 | HG01361.hp1 HG01884.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+4151_-14+4153d others(5): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 611234 | |||||
| chr18:611255
|
T | C | 5 | a0001c0001t0001g0076a0001c0001t0002g0006a0001c0001t0002g0100others(2): Show | 5 | HG01106.hp1 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+4156T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611255 | ||||||
| chr18:611321
|
G | T | 1 | a0001c0012t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-14+4222G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611321 | ||||||
| chr18:611322
|
C | A | 1 | a0001c0001t0006g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-14+4223C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611322 | ||||||
| chr18:611323
|
A | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0016others(234): Show | 239 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-14+4224A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611323 | ||||||
| chr18:611551
|
G | A | 1 | a0001c0012t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-14+4452G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611551 | ||||||
| chr18:611599
|
A | C | 1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-14+4500A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611599 | ||||||
| chr18:611790
|
T | A | 3 | a0001c0001t0001g0290a0001c0001t0002g0007a0001c0001t0004g0070 | 3 | HG02258.hp1 HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-14+4691T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611790 | ||||||
| chr18:611874
|
G | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(96): Show | 100 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-14+4775G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611874 | ||||||
| chr18:611889
|
T | C | 5 | a0001c0001t0001g0076a0001c0001t0002g0006a0001c0001t0002g0100others(2): Show | 5 | HG01106.hp1 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+4790T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611889 | ||||||
| chr18:611907
|
C | A | 1 | a0001c0001t0001g0087 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-14+4808C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611907 | ||||||
| chr18:611921
|
C | G | 5 | a0001c0001t0001g0076a0001c0001t0002g0006a0001c0001t0002g0100others(2): Show | 5 | HG01106.hp1 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+4822C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 611921 | ||||||
| chr18:612031
|
C | G | 2 | a0001c0001t0003g0340a0004c0003t0001g0075 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-14+4932C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 612031 | ||||||
| chr18:612431
|
G | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0051others(63): Show | 67 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.-14+5332G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 612431 | ||||||
| chr18:612454
|
A | G | 60 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0082others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.-14+5355A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 612454 | ||||||
| chr18:612569
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0003g0108 | 2 | HG00738.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-13-5419T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 612569 | ||||||
| chr18:612632
|
C | T | 1 | a0001c0001t0001g0363 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-13-5356C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 612632 | ||||||
| chr18:612710
|
C | T | 6 | a0001c0001t0001g0146a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG02056.hp1 NA18970.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-5278C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 612710 | ||||||
| chr18:612753
|
T | C | 172 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0052others(169): Show | 172 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.-13-5235T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 612753 | ||||||
| chr18:612767
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-13-5221C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 612767 | ||||||
| chr18:612809
|
C | T | 1 | a0001c0012t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-13-5179C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 612809 | ||||||
| chr18:612819
|
T | C | 113 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0066others(110): Show | 113 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-13-5169T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 612819 | ||||||
| chr18:612909
|
T | C | 4 | a0001c0001t0001g0286a0001c0001t0004g0138a0001c0001t0004g0140others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-5079T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 612909 | ||||||
| chr18:613020
|
G | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0050others(240): Show | 245 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.-13-4968G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613020 | ||||||
| chr18:613147
|
AT | A | 403 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(400): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.-13-4833delT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 613147 | |||||
| chr18:613148
|
T | G | 1 | a0001c0001t0001g0353 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-13-4840T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613148 | ||||||
| chr18:613202
|
A | G | 102 | a0001c0001t0001g0004a0001c0001t0001g0069a0001c0001t0001g0073others(99): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-13-4786A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613202 | ||||||
| chr18:613221
|
C | T | 1 | a0001c0001t0004g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-13-4767C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613221 | ||||||
| chr18:613229
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-13-4759C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613229 | ||||||
| chr18:613262
|
T | C | 2 | a0001c0001t0004g0070a0002c0005t0001g0125 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-13-4726T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613262 | ||||||
| chr18:613279
|
T | C | 1 | a0001c0001t0004g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-13-4709T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613279 | ||||||
| chr18:613283
|
T | C | 1 | a0001c0001t0004g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-13-4705T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613283 | ||||||
| chr18:613285
|
C | T | 2 | a0001c0001t0002g0334a0001c0001t0002g0335 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-13-4703C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613285 | ||||||
| chr18:613286
|
G | C | 1 | a0001c0001t0004g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-13-4702G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613286 | ||||||
| chr18:613389
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026 | 3 | NA18948.hp1 NA18966.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-13-4599C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613389 | ||||||
| chr18:613458
|
A | AT | 78 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0001g0065others(75): Show | 79 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-13-4516dupT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 613458 | |||||
| chr18:613515
|
C | T | 69 | a0001c0001t0001g0005a0001c0001t0001g0065a0001c0001t0001g0067others(66): Show | 70 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.-13-4473C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613515 | ||||||
| chr18:613541
|
G | A | 3 | a0001c0001t0003g0106a0001c0001t0004g0141a0004c0003t0001g0075 | 3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-13-4447G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613541 | ||||||
| chr18:613633
|
T | C | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG00639.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-13-4355T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613633 | ||||||
| chr18:613873
|
A | G | 16 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0278others(13): Show | 16 | HG01106.hp1 HG01167.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-13-4115A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 613873 | ||||||
| chr18:614079
|
C | T | 1 | a0001c0001t0003g0322 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-13-3909C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 614079 | ||||||
| chr18:614107
|
A | T | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0110others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-3881A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 614107 | ||||||
| chr18:614264
|
T | C | 1 | a0001c0001t0003g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-13-3724T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 614264 | ||||||
| chr18:614315
|
GAGGGAGG others(6): Show |
G | 2 | a0001c0001t0003g0104a0001c0001t0004g0070 | 2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-13-3656_-13-3644d others(15): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 614315 | |||||
| chr18:614317
|
GGGAGGGA others(1): Show |
G | 3 | a0001c0001t0003g0114a0001c0001t0003g0115a0001c0001t0003g0139 | 3 | HG01167.hp2 HG01169.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-13-3667_-13-3660d others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 614317 | |||||
| chr18:614321
|
G | GGGAA | 3 | a0001c0001t0003g0109a0001c0001t0003g0113a0001c0001t0004g0312 | 3 | HG01361.hp1 HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-13-3660_-13-3657d others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 614321 | |||||
| chr18:614321
|
GGGAAGGA others(30): Show |
G | 1 | a0001c0001t0001g0083 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-13-3656_-13-3620d others(39): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 614321 | |||||
| chr18:614328
|
A | AAAGG | 8 | a0001c0001t0001g0263a0001c0001t0001g0266a0001c0001t0001g0268others(5): Show | 8 | HG02451.hp2 HG02723.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-3659_-13-3658i others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 614328 | |||||
| chr18:614334
|
G | A | 9 | a0001c0001t0001g0263a0001c0001t0001g0266a0001c0001t0001g0268others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13-3654G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 614334 | ||||||
| chr18:614334
|
G | GGGAA | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(324): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.-13-3641_-13-3638d others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 614334 | |||||
| chr18:614351
|
A | G | 27 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0124others(24): Show | 27 | HG00738.hp2 HG01109.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-13-3637A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 614351 | ||||||
| chr18:614355
|
G | A | 27 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0124others(24): Show | 27 | HG00738.hp2 HG01109.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-13-3633G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 614355 | ||||||
| chr18:614422
|
A | G | 4 | a0001c0001t0001g0047a0001c0001t0003g0116a0001c0001t0003g0343others(1): Show | 4 | HG01891.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-3566A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 614422 | ||||||
| chr18:614449
|
C | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.-13-3539C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 614449 | ||||||
| chr18:614708
|
G | A | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(178): Show | 184 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.-13-3280G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 614708 | ||||||
| chr18:614941
|
C | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0152a0001c0001t0001g0237 | 3 | HG02896.hp1 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-13-3047C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 614941 | ||||||
| chr18:614955
|
C | T | 29 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0122others(26): Show | 29 | HG00323.hp1 HG00741.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-13-3033C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 614955 | ||||||
| chr18:615003
|
C | A | 1 | a0001c0001t0003g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-13-2985C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615003 | ||||||
| chr18:615014
|
C | A | 31 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0085others(28): Show | 31 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.-13-2974C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615014 | ||||||
| chr18:615063
|
A | G | 1 | a0004c0003t0001g0366 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13-2925A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615063 | ||||||
| chr18:615093
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-13-2895A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615093 | ||||||
| chr18:615177
|
G | A | 1 | a0001c0001t0004g0054 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-13-2811G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615177 | ||||||
| chr18:615181
|
C | G | 2 | a0001c0001t0001g0296a0001c0001t0001g0349 | 2 | HG01074.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-13-2807C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615181 | ||||||
| chr18:615368
|
T | C | 11 | a0001c0001t0001g0209a0001c0001t0001g0278a0001c0001t0002g0008others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13-2620T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615368 | ||||||
| chr18:615370
|
T | C | 1 | a0001c0001t0002g0331 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-13-2618T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615370 | ||||||
| chr18:615372
|
C | G | 1 | a0001c0001t0001g0393 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-13-2616C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615372 | ||||||
| chr18:615394
|
T | C | 317 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(314): Show | 320 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.-13-2594T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615394 | ||||||
| chr18:615499
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-13-2489G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615499 | ||||||
| chr18:615558
|
T | C | 1 | a0001c0001t0002g0336 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-13-2430T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615558 | ||||||
| chr18:615561
|
A | G | 1 | a0001c0001t0001g0393 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-13-2427A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615561 | ||||||
| chr18:615616
|
T | C | 1 | a0001c0001t0001g0275 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-13-2372T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615616 | ||||||
| chr18:615650
|
T | C | 11 | a0001c0001t0001g0209a0001c0001t0001g0278a0001c0001t0002g0008others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13-2338T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615650 | ||||||
| chr18:615691
|
T | C | 11 | a0001c0001t0001g0209a0001c0001t0001g0278a0001c0001t0002g0008others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13-2297T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615691 | ||||||
| chr18:615959
|
T | C | 1 | a0001c0004t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-13-2029T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 615959 | ||||||
| chr18:616072
|
T | G | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(376): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.-13-1916T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616072 | ||||||
| chr18:616077
|
A | G | 376 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(373): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.-13-1911A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616077 | ||||||
| chr18:616116
|
G | A | 3 | a0001c0002t0001g0270a0001c0002t0001g0285a0001c0002t0003g0105 | 3 | HG02922.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-13-1872G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616116 | ||||||
| chr18:616136
|
G | T | 3 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0106 | 3 | HG02895.hp2 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-13-1852G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616136 | ||||||
| chr18:616165
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18962.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-13-1823T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616165 | ||||||
| chr18:616195
|
C | T | 6 | a0001c0001t0002g0008a0001c0001t0003g0107a0001c0001t0003g0313others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-1793C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616195 | ||||||
| chr18:616288
|
A | C | 2 | a0001c0002t0001g0270a0001c0002t0001g0285 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-13-1700A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616288 | ||||||
| chr18:616317
|
G | A | 382 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(379): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.-13-1671G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616317 | ||||||
| chr18:616348
|
G | A | 382 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(379): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.-13-1640G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616348 | ||||||
| chr18:616385
|
G | A | 3 | a0001c0001t0003g0109a0001c0001t0004g0314a0002c0005t0001g0125 | 3 | HG01361.hp1 HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-13-1603G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616385 | ||||||
| chr18:616459
|
A | G | 1 | a0001c0001t0001g0383 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-13-1529A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616459 | ||||||
| chr18:616576
|
G | A | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(376): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.-13-1412G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616576 | ||||||
| chr18:616582
|
T | C | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(376): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.-13-1406T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616582 | ||||||
| chr18:616601
|
G | A | 3 | a0001c0001t0003g0109a0001c0001t0004g0314a0002c0005t0001g0125 | 3 | HG01361.hp1 HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-13-1387G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616601 | ||||||
| chr18:616653
|
C | T | 377 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(374): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.-13-1335C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616653 | ||||||
| chr18:616712
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-13-1276G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616712 | ||||||
| chr18:616751
|
T | C | 3 | a0001c0001t0003g0109a0001c0001t0004g0314a0002c0005t0001g0125 | 3 | HG01361.hp1 HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-13-1237T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616751 | ||||||
| chr18:616783
|
T | A | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(371): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-13-1205T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 616783 | ||||||
| chr18:617011
|
C | A | 5 | a0001c0001t0001g0072a0001c0001t0001g0223a0001c0001t0001g0283others(2): Show | 5 | HG02055.hp1 HG02809.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-977C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 617011 | ||||||
| chr18:617110
|
A | G | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(371): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-13-878A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 617110 | ||||||
| chr18:617129
|
T | A | 1 | a0001c0001t0001g0407 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-13-859T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 617129 | ||||||
| chr18:617338
|
T | C | 9 | a0001c0001t0001g0209a0001c0001t0002g0006a0001c0001t0002g0008others(6): Show | 9 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13-650T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 617338 | ||||||
| chr18:617408
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | NA18953.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-13-580C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 617408 | ||||||
| chr18:617412
|
T | C | 1 | a0001c0001t0004g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13-576T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 617412 | ||||||
| chr18:617572
|
G | A | 26 | a0001c0001t0001g0049a0001c0001t0001g0076a0001c0001t0001g0122others(23): Show | 26 | HG00323.hp1 HG00741.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-13-416G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 617572 | ||||||
| chr18:617595
|
C | CA | 253 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0025others(250): Show | 255 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.-13-373dupA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 617595 | |||||
| chr18:617595
|
C | CAA | 20 | a0001c0001t0001g0074a0001c0001t0001g0088a0001c0001t0001g0172others(17): Show | 20 | HG00438.hp2 HG00673.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13-374_-13-373dup others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 617595 | |||||
| chr18:617595
|
CA | C | 12 | a0001c0001t0002g0100a0001c0001t0003g0114a0001c0001t0003g0115others(9): Show | 12 | HG00323.hp1 HG01106.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.-13-373delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 617595 | |||||
| chr18:617614
|
A | AG | 6 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0096others(3): Show | 6 | HG00423.hp2 HG01928.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-374_-13-373ins others(1): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 617614 | ||||||
| chr18:617737
|
T | G | 2 | a0001c0001t0001g0238a0001c0001t0003g0139 | 2 | HG01109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-13-251T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 617737 | ||||||
| chr18:617772
|
G | A | 2 | a0001c0001t0003g0114a0001c0001t0003g0115 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-13-216G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 617772 | ||||||
| chr18:617775
|
AAG | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0042others(188): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.-13-210_-13-209del others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 617775 | |||||
| chr18:617928
|
A | T | 12 | a0001c0001t0001g0209a0001c0001t0002g0006a0001c0001t0002g0008others(9): Show | 12 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13-60A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 2/9 | chr18 | 617928 | ||||||
| chr18:618124
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0042others(189): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.106+18T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | chr18 | 618124 | ||||||
| chr18:618201
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.106+95C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | chr18 | 618201 | ||||||
| chr18:618243
|
GTCATCCT others(45): Show |
G | 1 | a0001c0001t0001g0234 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.106+139_106+190del others(52): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr18 | 618243 | |||||
| chr18:618249
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.106+143C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | chr18 | 618249 | ||||||
| chr18:618260
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.106+154C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | chr18 | 618260 | ||||||
| chr18:618398
|
C | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0179 | 3 | NA18962.hp2 NA19000.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.106+292C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | chr18 | 618398 | ||||||
| chr18:618708
|
G | C | 1 | a0001c0001t0003g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.107-505G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | chr18 | 618708 | ||||||
| chr18:618741
|
G | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0368a0001c0001t0002g0044others(9): Show | 13 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.107-472G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | chr18 | 618741 | ||||||
| chr18:618957
|
C | T | 3 | a0001c0002t0001g0270a0001c0002t0001g0285a0001c0002t0003g0105 | 3 | HG02922.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.107-256C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | chr18 | 618957 | ||||||
| chr18:619050
|
G | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(214): Show | 220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.107-163G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | chr18 | 619050 | ||||||
| chr18:619053
|
C | A | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0405 | 3 | HG02486.hp2 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.107-160C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | chr18 | 619053 | ||||||
| chr18:619125
|
C | T | 1 | a0001c0001t0001g0388 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.107-88C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | chr18 | 619125 | ||||||
| chr18:619154
|
A | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0151a0001c0001t0001g0203others(7): Show | 11 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-59A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 3/9 | chr18 | 619154 | ||||||
| chr18:619567
|
C | T | 1 | a0001c0001t0006g0121 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.255+206C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 619567 | ||||||
| chr18:619664
|
G | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0286 | 2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.255+303G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 619664 | ||||||
| chr18:619669
|
GT | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(158): Show | 162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.255+319delT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 619669 | |||||
| chr18:619740
|
G | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(176): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.255+379G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 619740 | ||||||
| chr18:619929
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.255+568C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 619929 | ||||||
| chr18:619955
|
C | A | 1 | a0001c0004t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.255+594C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 619955 | ||||||
| chr18:619959
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.255+598C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 619959 | ||||||
| chr18:619999
|
C | T | 1 | a0001c0001t0001g0388 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.255+638C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 619999 | ||||||
| chr18:620089
|
T | C | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.255+728T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 620089 | ||||||
| chr18:620164
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.255+803G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 620164 | ||||||
| chr18:620191
|
A | C | 11 | a0001c0001t0001g0074a0001c0001t0001g0263a0001c0001t0001g0266others(8): Show | 11 | HG01361.hp1 HG02109.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.255+830A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 620191 | ||||||
| chr18:620224
|
C | T | 1 | a0001c0001t0001g0365 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.255+863C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 620224 | ||||||
| chr18:620358
|
T | G | 3 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0291 | 3 | HG00609.hp1 NA18968.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.255+997T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 620358 | ||||||
| chr18:620364
|
G | GT | 6 | a0001c0001t0001g0050a0001c0001t0001g0133a0001c0001t0001g0238others(3): Show | 6 | HG01109.hp1 HG01884.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+1016dupT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 620364 | |||||
| chr18:620432
|
T | C | 2 | a0001c0001t0003g0322a0001c0001t0006g0121 | 2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.255+1071T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 620432 | ||||||
| chr18:620527
|
T | C | 1 | a0001c0001t0001g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.255+1166T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 620527 | ||||||
| chr18:620669
|
G | C | 1 | a0007c0007t0001g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.255+1308G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 620669 | ||||||
| chr18:620695
|
T | C | 407 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(404): Show | 412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.255+1334T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 620695 | ||||||
| chr18:620709
|
A | C | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.255+1348A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 620709 | ||||||
| chr18:620710
|
A | G | 1 | a0001c0001t0001g0377 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.255+1349A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 620710 | ||||||
| chr18:621244
|
A | G | 1 | a0001c0001t0001g0362 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.255+1883A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 621244 | ||||||
| chr18:621281
|
A | G | 405 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(402): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.255+1920A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 621281 | ||||||
| chr18:621300
|
G | C | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(371): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.255+1939G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 621300 | ||||||
| chr18:621321
|
G | A | 1 | a0001c0001t0006g0121 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.255+1960G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 621321 | ||||||
| chr18:621739
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.255+2378C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 621739 | ||||||
| chr18:621743
|
A | C | 2 | a0001c0001t0001g0215a0001c0001t0001g0220 | 2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.255+2382A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 621743 | ||||||
| chr18:621808
|
C | T | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.255+2447C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 621808 | ||||||
| chr18:622048
|
G | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 89 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.255+2687G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 622048 | ||||||
| chr18:622064
|
C | A | 1 | a0001c0012t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.255+2703C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 622064 | ||||||
| chr18:622384
|
T | C | 5 | a0001c0001t0001g0278a0001c0001t0003g0313a0001c0001t0003g0322others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-2481T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 622384 | ||||||
| chr18:622387
|
G | A | 1 | a0001c0001t0002g0035 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.256-2478G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 622387 | ||||||
| chr18:622494
|
T | A | 405 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(402): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.256-2371T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 622494 | ||||||
| chr18:622591
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 89 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.256-2274T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 622591 | ||||||
| chr18:622613
|
A | G | 1 | a0001c0001t0001g0388 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.256-2252A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 622613 | ||||||
| chr18:622694
|
GA | G | 3 | a0001c0001t0001g0080a0001c0001t0003g0108a0001c0001t0003g0341 | 3 | HG01167.hp1 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.256-2169delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 622694 | |||||
| chr18:622793
|
G | C | 1 | a0001c0001t0001g0407 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.256-2072G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 622793 | ||||||
| chr18:622820
|
G | T | 1 | a0001c0001t0001g0173 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.256-2045G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 622820 | ||||||
| chr18:622834
|
G | A | 391 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(388): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.256-2031G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 622834 | ||||||
| chr18:623034
|
C | CTT | 385 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(382): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.256-1817_256-1816d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 623034 | |||||
| chr18:623034
|
C | CTTTTTTT others(39): Show |
1 | a0001c0001t0001g0234 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.256-1816_256-1815i others(48): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 623034 | |||||
| chr18:623332
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.256-1533C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 623332 | ||||||
| chr18:623440
|
T | G | 1 | a0001c0001t0001g0187 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.256-1425T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 623440 | ||||||
| chr18:623644
|
C | CA | 13 | a0001c0001t0001g0074a0001c0001t0001g0266a0001c0001t0001g0268others(10): Show | 13 | HG01361.hp1 HG02109.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.256-1196dupA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 623644 | |||||
| chr18:623644
|
CA | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 100 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.256-1196delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 623644 | |||||
| chr18:623644
|
CAA | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.256-1197_256-1196d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 623644 | |||||
| chr18:623644
|
CAAA | C | 184 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0052others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.256-1198_256-1196d others(5): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 623644 | |||||
| chr18:623644
|
CAAAA | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0130a0001c0001t0001g0191others(2): Show | 6 | HG01106.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-1199_256-1196d others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 623644 | |||||
| chr18:623673
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.256-1192G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 623673 | ||||||
| chr18:623709
|
A | G | 5 | a0001c0001t0001g0278a0001c0001t0003g0313a0001c0001t0003g0322others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-1156A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 623709 | ||||||
| chr18:623773
|
C | T | 10 | a0001c0001t0001g0077a0001c0001t0001g0123a0001c0001t0001g0267others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.256-1092C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 623773 | ||||||
| chr18:623784
|
C | G | 405 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(402): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.256-1081C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 623784 | ||||||
| chr18:623827
|
A | C | 1 | a0001c0012t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.256-1038A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 623827 | ||||||
| chr18:623894
|
T | TTAATACT others(7): Show |
1 | a0001c0001t0002g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.256-970_256-957dup others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 623894 | |||||
| chr18:624002
|
G | C | 2 | a0001c0001t0003g0313a0001c0001t0003g0322 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.256-863G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 624002 | ||||||
| chr18:624333
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.256-532G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 624333 | ||||||
| chr18:624390
|
T | G | 68 | a0001c0001t0001g0052a0001c0001t0001g0069a0001c0001t0001g0072others(65): Show | 68 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.256-475T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 624390 | ||||||
| chr18:624631
|
T | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(191): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.256-234T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 624631 | ||||||
| chr18:624783
|
A | G | 405 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(402): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.256-82A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 624783 | ||||||
| chr18:624786
|
C | G | 1 | a0001c0001t0001g0163 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.256-79C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 624786 | ||||||
| chr18:624824
|
T | C | 391 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(388): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.256-41T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 4/9 | chr18 | 624824 | ||||||
| chr18:625056
|
A | T | 4 | a0001c0001t0001g0269a0001c0001t0001g0389a0001c0001t0003g0104others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+24A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 625056 | ||||||
| chr18:625070
|
G | A | 405 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(402): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.423+38G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 625070 | ||||||
| chr18:625145
|
C | T | 10 | a0001c0001t0001g0077a0001c0001t0001g0123a0001c0001t0001g0267others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.423+113C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 625145 | ||||||
| chr18:625206
|
T | A | 2 | a0001c0001t0001g0278a0003c0006t0004g0317 | 2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.423+174T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 625206 | ||||||
| chr18:625319
|
G | A | 9 | a0001c0001t0001g0050a0001c0001t0001g0122a0001c0001t0001g0265others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.423+287G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 625319 | ||||||
| chr18:625513
|
T | C | 1 | a0001c0001t0001g0388 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.423+481T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 625513 | ||||||
| chr18:625518
|
A | AAC | 21 | a0001c0001t0001g0131a0001c0001t0001g0188a0001c0001t0001g0217others(18): Show | 21 | HG00140.hp2 HG01074.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.423+527_423+528dup others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 625518 | |||||
| chr18:625518
|
A | AACAC | 25 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0001g0077others(22): Show | 26 | HG00735.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.423+525_423+528dup others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 625518 | |||||
| chr18:625518
|
A | AACACAC | 39 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0074others(36): Show | 40 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.423+523_423+528dup others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 625518 | |||||
| chr18:625518
|
A | AACACACA others(1): Show |
5 | a0001c0001t0001g0151a0001c0001t0001g0203a0001c0001t0001g0391others(2): Show | 5 | HG00544.hp2 HG02080.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+521_423+528dup others(8): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 625518 | |||||
| chr18:625518
|
A | AACACACA others(3): Show |
2 | a0001c0001t0003g0117a0001c0004t0001g0281 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.423+519_423+528dup others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 625518 | |||||
| chr18:625518
|
AAC | A | 23 | a0001c0001t0001g0025a0001c0001t0001g0049a0001c0001t0001g0076others(20): Show | 23 | HG01069.hp2 HG01891.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.423+527_423+528del others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 625518 | |||||
| chr18:625518
|
AACAC | A | 23 | a0001c0001t0001g0073a0001c0001t0001g0087a0001c0001t0001g0095others(20): Show | 23 | HG00323.hp2 HG00609.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.423+525_423+528del others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 625518 | |||||
| chr18:625518
|
AACACAC | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.423+523_423+528del others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 625518 | |||||
| chr18:625518
|
AACACACA others(3): Show |
A | 10 | a0001c0001t0001g0152a0001c0001t0001g0237a0001c0001t0001g0269others(7): Show | 10 | HG01884.hp2 HG02630.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.423+519_423+528del others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 625518 | |||||
| chr18:625555
|
ACACAC | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0376others(1): Show | 4 | HG01255.hp2 HG04204.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+525_423+529del others(5): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 625555 | |||||
| chr18:625766
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.423+734C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 625766 | ||||||
| chr18:625820
|
G | A | 376 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(373): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.423+788G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 625820 | ||||||
| chr18:625842
|
A | ATGAATG | 21 | a0001c0001t0001g0004a0001c0001t0001g0076a0001c0001t0001g0098others(18): Show | 22 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.423+810_423+811ins others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 625842 | ||||||
| chr18:625845
|
A | C | 21 | a0001c0001t0001g0004a0001c0001t0001g0076a0001c0001t0001g0098others(18): Show | 22 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.423+813A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 625845 | ||||||
| chr18:625861
|
C | T | 17 | a0001c0001t0001g0088a0001c0001t0001g0129a0001c0001t0001g0130others(14): Show | 17 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.423+829C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 625861 | ||||||
| chr18:625939
|
T | G | 14 | a0001c0001t0001g0074a0001c0001t0001g0263a0001c0001t0001g0266others(11): Show | 14 | HG01192.hp1 HG01361.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.423+907T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 625939 | ||||||
| chr18:626203
|
C | G | 2 | a0001c0001t0001g0355a0001c0001t0002g0029 | 2 | NA18955.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.424-894C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626203 | ||||||
| chr18:626212
|
A | G | 3 | a0001c0001t0003g0114a0001c0001t0003g0115a0001c0001t0006g0121 | 3 | HG01167.hp2 HG01169.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.424-885A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626212 | ||||||
| chr18:626383
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.424-714T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626383 | ||||||
| chr18:626518
|
C | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.424-579C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626518 | ||||||
| chr18:626580
|
C | T | 1 | a0001c0001t0004g0141 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.424-517C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626580 | ||||||
| chr18:626657
|
G | A | 63 | a0001c0001t0001g0052a0001c0001t0001g0069a0001c0001t0001g0072others(60): Show | 63 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.424-440G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626657 | ||||||
| chr18:626750
|
A | T | 3 | a0001c0001t0003g0114a0001c0001t0003g0115a0001c0001t0006g0121 | 3 | HG01167.hp2 HG01169.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.424-347A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626750 | ||||||
| chr18:626775
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.424-322C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626775 | ||||||
| chr18:626859
|
T | G | 3 | a0001c0001t0001g0305a0001c0001t0001g0372a0001c0001t0001g0375 | 3 | HG02698.hp2 HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.424-238T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626859 | ||||||
| chr18:626860
|
C | A | 3 | a0001c0001t0001g0305a0001c0001t0001g0372a0001c0001t0001g0375 | 3 | HG02698.hp2 HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.424-237C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626860 | ||||||
| chr18:626860
|
C | G | 1 | a0001c0001t0001g0160 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.424-237C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626860 | ||||||
| chr18:626863
|
A | AG | 20 | a0001c0001t0001g0085a0001c0001t0001g0091a0001c0001t0001g0093others(17): Show | 20 | HG00140.hp1 HG00733.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.424-234_424-233ins others(1): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626863 | ||||||
| chr18:626863
|
A | G | 3 | a0001c0001t0001g0305a0001c0001t0001g0372a0001c0001t0001g0375 | 3 | HG02698.hp2 HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.424-234A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626863 | ||||||
| chr18:626864
|
T | A | 23 | a0001c0001t0001g0085a0001c0001t0001g0091a0001c0001t0001g0093others(20): Show | 23 | HG00140.hp1 HG00733.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.424-233T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626864 | ||||||
| chr18:626864
|
T | TA | 9 | a0001c0001t0001g0042a0001c0001t0001g0067a0001c0001t0001g0247others(6): Show | 9 | HG00323.hp1 HG00438.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.424-231dupA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626864 | |||||
| chr18:626883
|
GAA | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.424-212_424-211del others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626883 | |||||
| chr18:626885
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0283a0001c0001t0001g0405 | 3 | HG02486.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.424-212A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626885 | ||||||
| chr18:626889
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.424-208A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626889 | ||||||
| chr18:626890
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0065 | 3 | HG01123.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.424-207A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626890 | ||||||
| chr18:626893
|
A | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.424-204A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626893 | ||||||
| chr18:626896
|
AAAGAAAG others(52): Show |
A | 1 | a0001c0001t0004g0312 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.424-197_424-139del others(59): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626896 | |||||
| chr18:626897
|
A | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.424-200A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626897 | ||||||
| chr18:626900
|
AAAGAAAG others(48): Show |
A | 1 | a0001c0001t0003g0113 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.424-193_424-139del others(55): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626900 | |||||
| chr18:626901
|
A | G | 1 | a0001c0004t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.424-196A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626901 | ||||||
| chr18:626907
|
GAA | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.424-188_424-187del others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626907 | |||||
| chr18:626908
|
AAAGAAAG others(44): Show |
A | 1 | a0001c0001t0001g0123 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.424-185_424-135del others(51): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626908 | |||||
| chr18:626912
|
AAAGAAAG others(32): Show |
A | 1 | a0001c0001t0001g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.424-181_424-143del others(39): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626912 | |||||
| chr18:626915
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.424-182G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626915 | ||||||
| chr18:626916
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.424-181A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626916 | ||||||
| chr18:626917
|
A | G | 1 | a0001c0001t0001g0405 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.424-180A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626917 | ||||||
| chr18:626919
|
G | A | 1 | a0001c0004t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.424-178G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626919 | ||||||
| chr18:626920
|
A | G | 1 | a0001c0004t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.424-177A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626920 | ||||||
| chr18:626924
|
AAAGAAGG others(75): Show |
A | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 82 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.424-172_424-91delA others(81): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626924 | ||||||
| chr18:626925
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0283 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.424-172A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626925 | ||||||
| chr18:626926
|
AGAAGGAA others(5): Show |
A | 1 | a0001c0001t0001g0370 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.424-167_424-156del others(12): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626926 | |||||
| chr18:626926
|
AGAAGGAA others(21): Show |
A | 1 | a0001c0001t0003g0341 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.424-163_424-136del others(28): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626926 | |||||
| chr18:626928
|
AAGGAAAG others(71): Show |
A | 1 | a0001c0004t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.424-168_424-91delA others(77): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626928 | ||||||
| chr18:626929
|
A | G | 1 | a0001c0001t0002g0347 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.424-168A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626929 | ||||||
| chr18:626930
|
G | A | 319 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.424-167G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626930 | ||||||
| chr18:626931
|
G | A | 1 | a0001c0001t0001g0405 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.424-166G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626931 | ||||||
| chr18:626932
|
AAAGAAGG others(4): Show |
A | 1 | a0001c0001t0001g0267 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.424-161_424-151del others(11): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626932 | |||||
| chr18:626933
|
A | G | 1 | a0001c0001t0002g0347 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.424-164A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626933 | ||||||
| chr18:626936
|
A | AG | 2 | a0001c0001t0001g0003a0001c0001t0001g0191 | 3 | HG01256.hp2 HG01258.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.424-161_424-160ins others(1): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626936 | ||||||
| chr18:626937
|
A | G | 1 | a0001c0001t0002g0347 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.424-160A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626937 | ||||||
| chr18:626938
|
G | A | 310 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.424-159G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626938 | ||||||
| chr18:626939
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0191a0001c0001t0001g0223others(1): Show | 5 | HG01256.hp2 HG01258.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-158G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626939 | ||||||
| chr18:626941
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424-156A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626941 | ||||||
| chr18:626942
|
A | G | 1 | a0001c0001t0002g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424-155A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626942 | ||||||
| chr18:626942
|
AGAAGGAA others(5): Show |
A | 1 | a0001c0001t0003g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.424-99_424-88delGG others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626942 | |||||
| chr18:626943
|
G | GA | 8 | a0001c0001t0001g0042a0001c0001t0001g0124a0001c0001t0001g0238others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.424-152dupA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626943 | |||||
| chr18:626943
|
GA | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0065 | 3 | HG01123.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.424-152delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626943 | |||||
| chr18:626944
|
AAGGAAGG | A | 3 | a0001c0001t0001g0164a0001c0001t0002g0332a0001c0001t0004g0316 | 3 | HG00423.hp1 HG03098.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.424-151_424-145del others(7): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626944 | |||||
| chr18:626944
|
AAGGAAGG others(4): Show |
A | 1 | a0001c0001t0001g0215 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.424-151_424-141del others(11): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626944 | |||||
| chr18:626944
|
AAGGAAGG others(55): Show |
A | 1 | a0001c0001t0001g0405 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.424-152_424-91delA others(61): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626944 | ||||||
| chr18:626945
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.424-152A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626945 | ||||||
| chr18:626946
|
G | A | 293 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.424-151G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626946 | ||||||
| chr18:626947
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0042others(11): Show | 16 | HG00738.hp2 HG01109.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.424-150G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626947 | ||||||
| chr18:626948
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0065 | 3 | HG01123.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.424-149A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626948 | ||||||
| chr18:626950
|
G | A | 291 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.424-147G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626950 | ||||||
| chr18:626950
|
GGAAGGAA others(48): Show |
G | 2 | a0001c0001t0001g0223a0001c0001t0001g0283 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.424-145_424-91delA others(54): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626950 | |||||
| chr18:626950
|
GGAAGGAA others(52): Show |
G | 2 | a0001c0001t0001g0003a0001c0001t0001g0191 | 3 | HG01256.hp2 HG01258.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.424-146_424-88delG others(58): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626950 | ||||||
| chr18:626951
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0047others(8): Show | 12 | HG00738.hp2 HG01109.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.424-146G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626951 | ||||||
| chr18:626953
|
A | G | 1 | a0001c0001t0002g0100 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.424-144A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626953 | ||||||
| chr18:626954
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(293): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.424-143G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626954 | ||||||
| chr18:626955
|
G | A | 9 | a0001c0001t0001g0042a0001c0001t0001g0124a0001c0001t0001g0164others(6): Show | 9 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.424-142G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626955 | ||||||
| chr18:626957
|
A | G | 2 | a0001c0001t0003g0341a0002c0005t0001g0125 | 2 | HG01167.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.424-140A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626957 | ||||||
| chr18:626958
|
G | A | 292 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.424-139G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626958 | ||||||
| chr18:626959
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0047others(11): Show | 15 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.424-138G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626959 | ||||||
| chr18:626960
|
AAGGAAGG others(11): Show |
A | 1 | a0001c0001t0002g0031 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.424-136_424-119del others(18): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626960 | ||||||
| chr18:626961
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.424-136A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626961 | ||||||
| chr18:626962
|
G | A | 289 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(286): Show | 289 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.424-135G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626962 | ||||||
| chr18:626962
|
GGAAGGAA others(40): Show |
G | 3 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0065 | 4 | HG01123.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-134_424-88delG others(46): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626962 | ||||||
| chr18:626963
|
G | A | 11 | a0001c0001t0001g0042a0001c0001t0001g0124a0001c0001t0001g0164others(8): Show | 11 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.424-134G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626963 | ||||||
| chr18:626963
|
GAAGGAAG others(22): Show |
G | 1 | a0002c0005t0001g0125 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.424-132_424-104del others(29): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626963 | |||||
| chr18:626964
|
A | G | 1 | a0001c0001t0002g0324 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.424-133A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626964 | ||||||
| chr18:626964
|
AAGGAAGG others(7): Show |
A | 4 | a0001c0001t0003g0106a0001c0001t0003g0114a0001c0001t0003g0115others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-132_424-119del others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626964 | ||||||
| chr18:626964
|
AAGGAAGG others(11): Show |
A | 1 | a0001c0001t0001g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.424-132_424-115del others(18): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626964 | ||||||
| chr18:626966
|
G | A | 279 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(276): Show | 279 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.424-131G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626966 | ||||||
| chr18:626967
|
G | A | 15 | a0001c0001t0001g0042a0001c0001t0001g0124a0001c0001t0001g0164others(12): Show | 15 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.424-130G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626967 | ||||||
| chr18:626968
|
AAGGAAGG others(3): Show |
A | 2 | a0001c0001t0002g0007a0001c0001t0006g0121 | 2 | HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.424-128_424-119del others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626968 | ||||||
| chr18:626970
|
G | A | 278 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(275): Show | 278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.424-127G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626970 | ||||||
| chr18:626970
|
GGAAGGAA others(32): Show |
G | 2 | a0001c0001t0001g0375a0001c0001t0003g0110 | 2 | HG02572.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.424-126_424-88delG others(38): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626970 | ||||||
| chr18:626971
|
G | A | 13 | a0001c0001t0001g0042a0001c0001t0001g0124a0001c0001t0001g0164others(10): Show | 13 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.424-126G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626971 | ||||||
| chr18:626972
|
AAGGAAGG others(3): Show |
A | 1 | a0001c0001t0001g0210 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.424-124_424-115del others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626972 | ||||||
| chr18:626972
|
AAGGAAGG others(7): Show |
A | 1 | a0001c0001t0001g0369 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424-124_424-111del others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626972 | ||||||
| chr18:626974
|
G | A | 273 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(270): Show | 273 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.424-123G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626974 | ||||||
| chr18:626975
|
G | A | 12 | a0001c0001t0001g0042a0001c0001t0001g0124a0001c0001t0001g0164others(9): Show | 12 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.424-122G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626975 | ||||||
| chr18:626976
|
AAG | A | 3 | a0001c0001t0001g0389a0001c0001t0003g0013a0001c0001t0003g0120 | 3 | HG02630.hp2 HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.424-120_424-119del others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626976 | ||||||
| chr18:626976
|
AAGGAAGG others(3): Show |
A | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.424-120_424-111del others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626976 | ||||||
| chr18:626978
|
G | A | 270 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(267): Show | 270 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.424-119G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626978 | ||||||
| chr18:626978
|
GGAAGGAA others(24): Show |
G | 2 | a0001c0001t0002g0100a0001c0001t0002g0324 | 2 | HG01106.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.424-118_424-88delG others(30): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626978 | ||||||
| chr18:626979
|
G | A | 12 | a0001c0001t0001g0042a0001c0001t0001g0124a0001c0001t0001g0164others(9): Show | 12 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.424-118G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626979 | ||||||
| chr18:626980
|
A | AGAG | 4 | a0001c0001t0001g0304a0001c0001t0002g0101a0001c0001t0003g0012others(1): Show | 4 | HG01070.hp2 HG01358.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-117_424-116ins others(3): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626980 | ||||||
| chr18:626980
|
AAGGAAG | A | 4 | a0001c0001t0001g0092a0001c0001t0002g0032a0001c0001t0002g0045others(1): Show | 4 | HG02165.hp1 HG03669.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-116_424-111del others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626980 | ||||||
| chr18:626981
|
A | G | 11 | a0001c0001t0001g0389a0001c0001t0002g0007a0001c0001t0002g0031others(8): Show | 11 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.424-116A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626981 | ||||||
| chr18:626982
|
G | A | 273 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.424-115G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626982 | ||||||
| chr18:626982
|
GGAAGGAA others(20): Show |
G | 2 | a0001c0001t0001g0306a0001c0001t0002g0039 | 2 | HG01952.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.424-114_424-88delG others(26): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626982 | ||||||
| chr18:626983
|
G | A | 14 | a0001c0001t0001g0042a0001c0001t0001g0124a0001c0001t0001g0164others(11): Show | 14 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.424-114G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626983 | ||||||
| chr18:626984
|
A | AGAG | 6 | a0001c0001t0001g0122a0001c0001t0003g0011a0001c0001t0003g0343others(3): Show | 6 | HG02135.hp1 HG02559.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.424-113_424-112ins others(3): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626984 | ||||||
| chr18:626985
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0279 | 2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.424-112A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626985 | ||||||
| chr18:626986
|
G | A | 266 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.424-111G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626986 | ||||||
| chr18:626987
|
G | A | 18 | a0001c0001t0001g0042a0001c0001t0001g0122a0001c0001t0001g0124others(15): Show | 18 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.424-110G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626987 | ||||||
| chr18:626988
|
A | AGAG | 4 | a0001c0001t0001g0050a0001c0001t0001g0364a0001c0001t0001g0393others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-109_424-108ins others(3): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626988 | ||||||
| chr18:626988
|
AAG | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0158a0001c0001t0001g0237others(2): Show | 5 | HG02074.hp2 HG02280.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-108_424-107del others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626988 | ||||||
| chr18:626989
|
A | G | 4 | a0001c0001t0001g0242a0001c0001t0002g0006a0001c0001t0003g0342others(1): Show | 4 | HG03209.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-108A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626989 | ||||||
| chr18:626990
|
G | A | 265 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.424-107G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626990 | ||||||
| chr18:626990
|
GGA | G | 4 | a0001c0001t0001g0304a0001c0001t0002g0101a0001c0001t0003g0012others(1): Show | 4 | HG01070.hp2 HG01358.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-106_424-105del others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626990 | ||||||
| chr18:626991
|
G | A | 19 | a0001c0001t0001g0042a0001c0001t0001g0050a0001c0001t0001g0122others(16): Show | 19 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.424-106G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626991 | ||||||
| chr18:626991
|
GA | G | 22 | a0001c0001t0001g0072a0001c0001t0001g0092a0001c0001t0001g0210others(19): Show | 22 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.424-104delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626991 | |||||
| chr18:626992
|
A | AAAG | 3 | a0001c0001t0001g0278a0001c0001t0002g0006a0001c0001t0003g0342 | 3 | HG02965.hp1 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.424-104_424-103ins others(3): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626992 | |||||
| chr18:626992
|
A | AG | 5 | a0001c0001t0001g0220a0001c0001t0002g0030a0001c0001t0002g0202others(2): Show | 5 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-105_424-104ins others(1): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626992 | ||||||
| chr18:626992
|
A | AGAAAG | 3 | a0001c0001t0001g0069a0001c0001t0001g0181a0001c0001t0001g0231 | 3 | HG00438.hp2 HG01099.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.424-105_424-104ins others(5): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626992 | ||||||
| chr18:626992
|
A | AGAG | 6 | a0001c0001t0001g0095a0001c0001t0001g0265a0001c0001t0001g0367others(3): Show | 6 | HG00741.hp1 HG01243.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-105_424-104ins others(3): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626992 | ||||||
| chr18:626992
|
A | G | 4 | a0001c0001t0001g0164a0001c0001t0001g0215a0001c0001t0002g0332others(1): Show | 4 | HG00423.hp1 HG00558.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-105A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626992 | ||||||
| chr18:626993
|
A | G | 4 | a0001c0001t0001g0152a0001c0001t0001g0237a0001c0001t0001g0242others(1): Show | 4 | HG02735.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-104A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626993 | ||||||
| chr18:626994
|
G | A | 233 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0025others(230): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.424-103G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626994 | ||||||
| chr18:626994
|
GGA | G | 7 | a0001c0001t0001g0122a0001c0001t0001g0364a0001c0001t0003g0011others(4): Show | 7 | HG02135.hp1 HG02559.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.424-102_424-101del others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626994 | ||||||
| chr18:626995
|
G | A | 56 | a0001c0001t0001g0042a0001c0001t0001g0050a0001c0001t0001g0069others(53): Show | 56 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.424-102G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626995 | ||||||
| chr18:626995
|
GA | G | 3 | a0001c0001t0001g0158a0001c0001t0002g0112a0001c0001t0004g0138 | 3 | HG02074.hp2 HG02280.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.424-100delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626995 | |||||
| chr18:626995
|
GAAGGAAG others(6): Show |
G | 1 | a0001c0001t0001g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.424-98_424-86delGA others(11): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626995 | |||||
| chr18:626996
|
A | AAAG | 3 | a0001c0001t0001g0025a0001c0001t0001g0214a0001c0011t0001g0071 | 3 | HG02027.hp2 HG03225.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.424-100_424-99insA others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626996 | |||||
| chr18:626996
|
A | AAAGAG | 9 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0157others(6): Show | 9 | HG01361.hp2 HG01975.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.424-100_424-99insA others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626996 | |||||
| chr18:626996
|
A | AAAGAGAG others(4): Show |
1 | a0001c0001t0004g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.424-100_424-99insA others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626996 | |||||
| chr18:626996
|
A | AAG | 3 | a0001c0001t0001g0050a0001c0001t0001g0393a0001c0001t0006g0264 | 3 | HG02109.hp2 HG02723.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.424-100_424-99dupA others(1): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 626996 | |||||
| chr18:626996
|
A | AG | 12 | a0001c0001t0001g0162a0001c0001t0001g0227a0001c0001t0001g0251others(9): Show | 12 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.424-101_424-100ins others(1): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626996 | ||||||
| chr18:626996
|
A | AGAAAG | 5 | a0001c0001t0001g0052a0001c0001t0001g0376a0001c0001t0002g0022others(2): Show | 5 | HG01255.hp2 HG01261.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-101_424-100ins others(5): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626996 | ||||||
| chr18:626996
|
A | AGAG | 10 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0134others(7): Show | 10 | HG01081.hp2 HG01884.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.424-101_424-100ins others(3): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626996 | ||||||
| chr18:626996
|
A | AGAGAAAG | 3 | a0001c0001t0001g0074a0001c0001t0003g0340a0001c0001t0006g0261 | 3 | HG02723.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.424-101_424-100ins others(7): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626996 | ||||||
| chr18:626998
|
G | A | 224 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.424-99G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626998 | ||||||
| chr18:626999
|
G | A | 68 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0049others(65): Show | 68 | HG00544.hp1 HG00609.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.424-98G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 626999 | ||||||
| chr18:627000
|
A | AG | 5 | a0001c0001t0001g0244a0001c0001t0001g0359a0001c0001t0001g0386others(2): Show | 5 | HG01106.hp2 NA18970.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.424-97_424-96insG | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627000 | ||||||
| chr18:627002
|
G | A | 228 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(225): Show | 228 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.424-95G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627002 | ||||||
| chr18:627002
|
G | GA | 6 | a0001c0001t0001g0238a0001c0001t0001g0244a0001c0001t0001g0359others(3): Show | 6 | HG01106.hp2 HG01109.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.424-95_424-94insA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627002 | ||||||
| chr18:627002
|
G | GAGAAAA | 7 | a0001c0001t0001g0095a0001c0001t0001g0242a0001c0001t0001g0265others(4): Show | 7 | HG00741.hp1 HG01243.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.424-95_424-94insAG others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627002 | ||||||
| chr18:627002
|
GGAAGGAA others(5): Show |
G | 1 | a0001c0001t0003g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.424-91_424-80delGG others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627002 | |||||
| chr18:627003
|
G | A | 53 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0069others(50): Show | 53 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.424-94G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627003 | ||||||
| chr18:627004
|
A | AG | 10 | a0001c0001t0001g0017a0001c0001t0001g0096a0001c0001t0001g0146others(7): Show | 10 | HG00621.hp2 HG01109.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.424-93_424-92insG | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627004 | ||||||
| chr18:627004
|
A | AGAAAG | 5 | a0001c0001t0001g0079a0001c0001t0001g0124a0001c0001t0002g0019others(2): Show | 5 | HG00738.hp2 NA18942.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.424-93_424-92insGA others(3): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627004 | ||||||
| chr18:627004
|
A | AGAAAGAA others(8): Show |
1 | a0001c0001t0001g0272 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.424-93_424-92insGA others(13): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627004 | ||||||
| chr18:627004
|
A | AGAGAGAA others(6): Show |
11 | a0001c0001t0001g0066a0001c0001t0001g0133a0001c0001t0001g0166others(8): Show | 11 | HG00621.hp1 HG01109.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.424-93_424-92insGA others(11): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627004 | ||||||
| chr18:627005
|
A | AAGAGAG | 10 | a0001c0001t0001g0150a0001c0001t0001g0159a0001c0001t0001g0170others(7): Show | 10 | HG00558.hp2 HG01123.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.424-92_424-91insAG others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627005 | ||||||
| chr18:627005
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.424-92A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627005 | ||||||
| chr18:627006
|
G | A | 153 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0067others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.424-91G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627006 | ||||||
| chr18:627006
|
G | GA | 13 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0134others(10): Show | 13 | HG01081.hp2 HG01884.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.424-91_424-90insA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627006 | ||||||
| chr18:627006
|
GGAA | G | 40 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0092others(37): Show | 40 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.424-90_424-88delGA others(1): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627006 | ||||||
| chr18:627006
|
GGAAAGAA others(1): Show |
G | 3 | a0001c0001t0003g0117a0001c0001t0004g0070a0001c0001t0004g0310 | 3 | HG02572.hp2 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.424-74_424-67delGA others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627006 | |||||
| chr18:627006
|
GGAAAGAA others(9): Show |
G | 1 | a0001c0001t0002g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424-82_424-67delGA others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627006 | |||||
| chr18:627007
|
G | A | 89 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0050others(86): Show | 89 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.424-90G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627007 | ||||||
| chr18:627008
|
A | AAGAGAGA others(4): Show |
1 | a0001c0001t0001g0184 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.424-88_424-87insGA others(9): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627008 | |||||
| chr18:627008
|
A | AGAAAGAG others(5): Show |
7 | a0001c0001t0001g0235a0001c0001t0001g0239a0001c0001t0001g0381others(4): Show | 7 | HG00280.hp1 HG02129.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.424-89_424-88insGA others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627008 | ||||||
| chr18:627009
|
A | AAGAGAGA others(23): Show |
5 | a0001c0001t0001g0087a0001c0001t0001g0189a0001c0001t0001g0193others(2): Show | 5 | HG00323.hp2 HG01081.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.424-85_424-84insGA others(28): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627009 | |||||
| chr18:627009
|
A | AAGAGAGA others(23): Show |
1 | a0003c0006t0004g0317 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.424-85_424-84insGA others(28): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627009 | |||||
| chr18:627009
|
A | AG | 60 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0052others(57): Show | 60 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.424-88_424-87insG | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627009 | ||||||
| chr18:627009
|
A | G | 15 | a0001c0001t0001g0145a0001c0001t0001g0161a0001c0001t0001g0169others(12): Show | 15 | HG01192.hp1 HG01433.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.424-88A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627009 | ||||||
| chr18:627010
|
A | G | 6 | a0001c0001t0001g0077a0001c0001t0001g0123a0001c0001t0001g0267others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.424-87A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627010 | ||||||
| chr18:627011
|
G | A | 10 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0068others(7): Show | 10 | HG01081.hp2 HG01884.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.424-86G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627011 | ||||||
| chr18:627012
|
A | AGAAAAG | 9 | a0001c0001t0001g0144a0001c0001t0001g0244a0001c0001t0001g0263others(6): Show | 9 | HG01106.hp2 HG01975.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.424-85_424-84insGA others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627012 | ||||||
| chr18:627012
|
A | AGAAAGAG others(5): Show |
3 | a0001c0001t0001g0169a0001c0001t0001g0296a0001c0001t0001g0406 | 3 | HG00673.hp2 HG03927.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.424-85_424-84insGA others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627012 | ||||||
| chr18:627012
|
A | AGAGAGAA others(3): Show |
4 | a0001c0001t0001g0081a0001c0001t0001g0302a0001c0001t0001g0353others(1): Show | 4 | HG01257.hp2 HG01981.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-85_424-84insGA others(8): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627012 | ||||||
| chr18:627012
|
A | G | 9 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0068others(6): Show | 9 | HG01081.hp2 HG01884.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.424-85A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627012 | ||||||
| chr18:627013
|
A | AAAGAAAG others(24): Show |
1 | a0001c0001t0001g0382 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.424-83_424-82insAG others(29): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627013 | |||||
| chr18:627013
|
A | AAAGAAGA others(3): Show |
8 | a0001c0001t0001g0145a0001c0001t0001g0161a0001c0001t0001g0246others(5): Show | 8 | HG01433.hp1 HG02683.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.424-83_424-82insAG others(8): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627013 | |||||
| chr18:627013
|
A | AAG | 10 | a0001c0001t0001g0184a0001c0001t0001g0209a0001c0001t0001g0235others(7): Show | 10 | HG00280.hp1 HG02129.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.424-82_424-81dupGA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627013 | |||||
| chr18:627013
|
A | AAGAGAAA others(15): Show |
1 | a0001c0001t0001g0286 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.424-81_424-80insGA others(20): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627013 | |||||
| chr18:627013
|
A | AAGAGAAG others(20): Show |
1 | a0001c0001t0001g0178 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.424-81_424-80insGA others(25): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627013 | |||||
| chr18:627013
|
A | AAGAGAGA others(23): Show |
3 | a0001c0001t0001g0226a0001c0001t0001g0287a0001c0001t0002g0323 | 3 | HG00597.hp2 HG00733.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.424-81_424-80insGA others(28): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627013 | |||||
| chr18:627013
|
A | AAGAGAGA others(21): Show |
1 | a0001c0001t0001g0194 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.424-81_424-80insGA others(26): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627013 | |||||
| chr18:627013
|
A | AGAAAG | 30 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0079others(27): Show | 30 | HG00621.hp1 HG00621.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.424-84_424-83insGA others(3): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627013 | ||||||
| chr18:627013
|
A | G | 11 | a0001c0001t0001g0097a0001c0001t0001g0167a0001c0001t0001g0168others(8): Show | 11 | HG00673.hp1 HG02040.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.424-84A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627013 | ||||||
| chr18:627014
|
A | G | 7 | a0001c0001t0001g0077a0001c0001t0001g0123a0001c0001t0001g0267others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.424-83A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627014 | ||||||
| chr18:627015
|
G | GA | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 90 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.424-79dupA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627015 | |||||
| chr18:627015
|
G | GAGAAAAG others(5): Show |
12 | a0001c0001t0001g0150a0001c0001t0001g0159a0001c0001t0001g0170others(9): Show | 12 | HG00558.hp2 HG01123.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.424-81_424-80insGA others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627015 | |||||
| chr18:627015
|
G | GAGAAAGA others(4): Show |
1 | a0001c0001t0001g0387 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.424-81_424-80insGA others(9): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627015 | |||||
| chr18:627015
|
G | GAGAGAAA others(7): Show |
8 | a0001c0001t0001g0026a0001c0001t0001g0088a0001c0001t0001g0187others(5): Show | 8 | HG00738.hp1 HG02132.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.424-81_424-80insGA others(12): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627015 | |||||
| chr18:627015
|
G | GAGAGAGA others(9): Show |
4 | a0001c0001t0001g0135a0001c0001t0001g0371a0001c0001t0002g0126others(1): Show | 4 | HG01952.hp1 HG02080.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-81_424-80insGA others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627015 | |||||
| chr18:627017
|
A | AAAGAAGA others(3): Show |
6 | a0001c0001t0001g0097a0001c0001t0001g0167a0001c0001t0001g0168others(3): Show | 6 | HG00673.hp1 HG02040.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-79_424-78insAG others(8): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627017 | |||||
| chr18:627017
|
A | AAG | 28 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0068others(25): Show | 28 | HG00673.hp2 HG01081.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.424-78_424-77dupGA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627017 | |||||
| chr18:627017
|
A | AAGAGAAA others(9): Show |
1 | a0001c0001t0001g0247 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.424-77_424-76insGA others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627017 | |||||
| chr18:627017
|
A | AAGAGAAA others(15): Show |
3 | a0001c0001t0001g0155a0001c0001t0001g0229a0001c0001t0001g0248 | 3 | HG02027.hp1 NA18975.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.424-77_424-76insGA others(20): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627017 | |||||
| chr18:627017
|
A | AAGAGAGA others(11): Show |
5 | a0001c0001t0001g0016a0001c0001t0001g0084a0001c0001t0001g0213others(2): Show | 5 | HG02135.hp2 HG02148.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-77_424-76insGA others(16): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627017 | |||||
| chr18:627017
|
A | G | 30 | a0001c0001t0001g0026a0001c0001t0001g0088a0001c0001t0001g0135others(27): Show | 30 | HG00558.hp2 HG00738.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.424-80A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627017 | ||||||
| chr18:627018
|
A | G | 3 | a0001c0001t0001g0267a0001c0001t0004g0310a0001c0001t0004g0316 | 3 | HG01243.hp1 HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.424-79A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627018 | ||||||
| chr18:627019
|
G | C | 1 | a0001c0001t0001g0153 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.424-78G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627019 | ||||||
| chr18:627021
|
A | AAAG | 5 | a0001c0001t0001g0074a0001c0001t0003g0340a0001c0001t0004g0140others(2): Show | 5 | HG02615.hp1 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-75_424-74insAG others(1): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627021 | |||||
| chr18:627021
|
A | G | 8 | a0001c0001t0001g0082a0001c0001t0001g0241a0001c0001t0001g0256others(5): Show | 8 | HG01981.hp2 HG02056.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424-76A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627021 | ||||||
| chr18:627023
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 209 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.424-74G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627023 | ||||||
| chr18:627023
|
G | C | 1 | a0001c0001t0001g0275 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.424-74G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627023 | ||||||
| chr18:627023
|
G | GA | 54 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0079others(51): Show | 54 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.424-71dupA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627023 | |||||
| chr18:627023
|
G | GAGAAAAA others(19): Show |
1 | a0001c0001t0001g0365 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.424-73_424-72insGA others(24): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627023 | |||||
| chr18:627023
|
G | GAGAAAAG others(18): Show |
1 | a0001c0001t0002g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.424-73_424-72insGA others(23): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627023 | |||||
| chr18:627023
|
G | GAGAAAAG others(18): Show |
4 | a0001c0001t0001g0082a0001c0001t0001g0154a0001c0001t0001g0211others(1): Show | 4 | HG01981.hp2 HG02717.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-73_424-72insGA others(23): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627023 | |||||
| chr18:627023
|
G | GAGAAAAG others(24): Show |
2 | a0001c0001t0001g0266a0001c0001t0001g0268 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.424-73_424-72insGA others(29): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627023 | |||||
| chr18:627023
|
G | GAGAGAGA others(22): Show |
2 | a0001c0001t0001g0078a0001c0001t0001g0300 | 2 | HG00639.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.424-73_424-72insGA others(27): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627023 | |||||
| chr18:627023
|
G | GAGAGAGA others(32): Show |
3 | a0001c0001t0001g0089a0001c0001t0001g0171a0001c0001t0001g0195 | 3 | HG00735.hp1 HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.424-73_424-72insGA others(37): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627023 | |||||
| chr18:627023
|
G | GAGAGAGA others(28): Show |
2 | a0001c0001t0001g0183a0001c0001t0001g0388 | 2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.424-73_424-72insGA others(33): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627023 | |||||
| chr18:627024
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(109): Show | 114 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.424-73A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627024 | ||||||
| chr18:627025
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 96 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.424-72A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627025 | ||||||
| chr18:627027
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(109): Show | 114 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.424-70G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627027 | ||||||
| chr18:627027
|
G | GAGAAAAG others(26): Show |
1 | a0001c0001t0002g0196 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.424-69_424-68insGA others(31): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627027 | |||||
| chr18:627027
|
G | GAGAAAGA others(35): Show |
1 | a0001c0001t0001g0175 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.424-69_424-68insGA others(40): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627027 | |||||
| chr18:627027
|
G | GAGAAAGA others(31): Show |
1 | a0001c0001t0001g0233 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.424-69_424-68insGA others(36): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627027 | |||||
| chr18:627027
|
G | GAGAGAAA others(27): Show |
1 | a0001c0001t0001g0198 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.424-69_424-68insGA others(32): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627027 | |||||
| chr18:627027
|
G | GAGAGAGA others(39): Show |
1 | a0001c0001t0001g0090 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.424-69_424-68insGA others(44): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627027 | |||||
| chr18:627027
|
GA | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 90 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.424-66delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627027 | |||||
| chr18:627028
|
A | AAAAGAAA others(5): Show |
3 | a0001c0001t0001g0263a0001c0004t0003g0344a0001c0012t0001g0257 | 3 | HG01192.hp1 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.424-62_424-61insAA others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627028 | |||||
| chr18:627028
|
A | AG | 8 | a0001c0001t0001g0074a0001c0001t0001g0266a0001c0001t0001g0268others(5): Show | 8 | HG02615.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.424-69_424-68insG | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627028 | ||||||
| chr18:627028
|
A | AGAAAGAA others(15): Show |
2 | a0001c0001t0002g0128a0001c0001t0004g0314 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.424-69_424-68insGA others(20): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627028 | ||||||
| chr18:627028
|
A | AGAGAAAG others(37): Show |
1 | a0001c0001t0003g0109 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.424-69_424-68insGA others(42): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627028 | ||||||
| chr18:627030
|
A | AAAG | 67 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0078others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.424-66_424-65insAG others(1): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627030 | |||||
| chr18:627030
|
A | AAGAAAAA others(1): Show |
62 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0026others(59): Show | 62 | HG00558.hp2 HG00673.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.424-62_424-61insAA others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627030 | |||||
| chr18:627030
|
A | AAGAAGAA others(23): Show |
5 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0199others(2): Show | 5 | HG02148.hp1 HG03492.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-63_424-62insGA others(28): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 627030 | |||||
| chr18:627030
|
A | AGAAAGAA others(121): Show |
1 | a0001c0001t0001g0297 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(126): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(108): Show |
1 | a0001c0001t0001g0085 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(113): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(101): Show |
1 | a0001c0001t0004g0062 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(106): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(101): Show |
1 | a0001c0001t0004g0054 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(106): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(93): Show |
1 | a0001c0001t0001g0351 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(98): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(89): Show |
1 | a0001c0001t0001g0093 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(94): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(89): Show |
1 | a0001c0001t0004g0061 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(94): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(85): Show |
1 | a0001c0001t0001g0383 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(90): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(79): Show |
1 | a0001c0001t0001g0352 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(84): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(75): Show |
1 | a0001c0001t0001g0384 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(80): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(77): Show |
1 | a0001c0001t0001g0403 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(82): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(73): Show |
1 | a0001c0001t0001g0234 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(78): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(69): Show |
1 | a0001c0001t0002g0036 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(74): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(65): Show |
1 | a0001c0001t0002g0037 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(70): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(61): Show |
1 | a0001c0001t0001g0091 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(66): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(65): Show |
1 | a0001c0001t0001g0401 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(70): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(57): Show |
1 | a0001c0001t0001g0185 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(62): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(53): Show |
1 | a0001c0001t0001g0355 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(58): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(47): Show |
1 | a0001c0001t0001g0377 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(52): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(42): Show |
1 | a0001c0001t0001g0298 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(47): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(45): Show |
1 | a0001c0001t0001g0293 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(50): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(51): Show |
1 | a0001c0001t0001g0073 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(56): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(37): Show |
1 | a0001c0001t0001g0240 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(42): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAA others(39): Show |
1 | a0001c0001t0001g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(44): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAG others(35): Show |
2 | a0001c0001t0001g0216a0001c0001t0001g0299 | 2 | HG00408.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.424-67_424-66insGA others(40): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAAGAG others(36): Show |
1 | a0001c0001t0001g0083 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(41): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAAGAAA others(22): Show |
1 | a0001c0001t0001g0385 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(27): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAGAAAA others(29): Show |
5 | a0001c0001t0001g0241a0001c0001t0001g0256a0001c0001t0001g0363others(2): Show | 5 | HG02056.hp1 HG02451.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-67_424-66insGA others(34): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAGAGAA others(31): Show |
1 | a0001c0001t0001g0301 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(36): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAGAGAG others(33): Show |
1 | a0001c0001t0001g0354 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.424-67_424-66insGA others(38): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGAGAGAG others(43): Show |
1 | a0001c0001t0002g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGA others(48): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | AGGAAGAG others(37): Show |
1 | a0001c0001t0001g0067 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.424-67_424-66insGG others(42): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627030
|
A | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(116): Show | 121 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.424-67A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627030 | ||||||
| chr18:627044
|
C | T | 390 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(387): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.424-53C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 5/9 | chr18 | 627044 | ||||||
| chr18:627629
|
A | G | 391 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(388): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.856+100A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 627629 | ||||||
| chr18:627701
|
C | T | 390 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(387): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.856+172C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 627701 | ||||||
| chr18:627747
|
A | C | 1 | a0001c0001t0005g0027 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.856+218A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 627747 | ||||||
| chr18:627790
|
G | GA | 17 | a0001c0001t0001g0068a0001c0001t0001g0092a0001c0001t0001g0135others(14): Show | 17 | HG00099.hp1 HG00597.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.856+272dupA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 627790 | |||||
| chr18:627802
|
C | A | 1 | a0001c0012t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.856+273C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 627802 | ||||||
| chr18:627987
|
C | G | 10 | a0001c0001t0001g0077a0001c0001t0001g0123a0001c0001t0001g0267others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.856+458C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 627987 | ||||||
| chr18:628068
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0090a0001c0001t0002g0323 | 3 | HG00733.hp1 HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.856+539C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628068 | ||||||
| chr18:628372
|
T | C | 3 | a0001c0001t0001g0080a0001c0001t0003g0108a0001c0001t0003g0341 | 3 | HG01167.hp1 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.856+843T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628372 | ||||||
| chr18:628445
|
G | A | 16 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0123others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.856+916G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628445 | ||||||
| chr18:628487
|
C | A | 15 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0123others(12): Show | 15 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.856+958C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628487 | ||||||
| chr18:628543
|
G | C | 2 | a0001c0001t0003g0313a0001c0001t0003g0322 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.856+1014G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628543 | ||||||
| chr18:628547
|
C | G | 1 | a0001c0001t0005g0027 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.856+1018C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628547 | ||||||
| chr18:628639
|
C | CT | 21 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0089others(18): Show | 21 | HG01099.hp2 HG01109.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.856+1125dupT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 628639 | |||||
| chr18:628639
|
C | CTT | 7 | a0001c0001t0001g0077a0001c0001t0001g0123a0001c0001t0003g0113others(4): Show | 7 | HG01884.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.856+1124_856+1125d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 628639 | |||||
| chr18:628701
|
G | A | 7 | a0001c0001t0001g0077a0001c0001t0001g0123a0001c0001t0001g0360others(4): Show | 7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+1172G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628701 | ||||||
| chr18:628792
|
T | C | 1 | a0001c0004t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.856+1263T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628792 | ||||||
| chr18:628831
|
C | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0123a0001c0001t0003g0113others(1): Show | 4 | HG01884.hp1 HG02486.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+1302C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628831 | ||||||
| chr18:628872
|
A | T | 3 | a0001c0001t0001g0080a0001c0001t0003g0108a0001c0001t0003g0341 | 3 | HG01167.hp1 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.856+1343A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628872 | ||||||
| chr18:628883
|
T | A | 1 | a0001c0001t0004g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.856+1354T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628883 | ||||||
| chr18:628915
|
G | GAGCCACC others(10): Show |
1 | a0001c0001t0001g0400 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.856+1413_856+1429d others(19): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 628915 | |||||
| chr18:628915
|
GAGCCACC others(10): Show |
G | 3 | a0001c0001t0001g0238a0001c0001t0001g0373a0001c0001t0001g0374 | 3 | HG01109.hp1 HG02683.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.856+1413_856+1429d others(19): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 628915 | |||||
| chr18:628971
|
C | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0283a0001c0001t0001g0405 | 3 | HG02486.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.856+1442C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628971 | ||||||
| chr18:628980
|
T | C | 79 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0079others(76): Show | 79 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.856+1451T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628980 | ||||||
| chr18:628985
|
A | G | 4 | a0001c0001t0001g0135a0001c0001t0001g0165a0001c0001t0001g0357others(1): Show | 4 | NA18957.hp1 NA18967.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.856+1456A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 628985 | ||||||
| chr18:629029
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.856+1500A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 629029 | ||||||
| chr18:629035
|
A | G | 75 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0079others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.856+1506A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 629035 | ||||||
| chr18:629187
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.856+1658G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 629187 | ||||||
| chr18:629239
|
C | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.856+1710C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 629239 | ||||||
| chr18:629360
|
C | T | 22 | a0001c0001t0001g0079a0001c0001t0001g0089a0001c0001t0001g0145others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.856+1831C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 629360 | ||||||
| chr18:629381
|
C | T | 1 | a0001c0001t0002g0329 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.856+1852C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 629381 | ||||||
| chr18:629794
|
C | T | 6 | a0001c0001t0001g0080a0001c0001t0001g0210a0001c0001t0001g0370others(3): Show | 6 | HG02886.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.856+2265C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 629794 | ||||||
| chr18:630005
|
A | C | 137 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0068others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.856+2476A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630005 | ||||||
| chr18:630041
|
T | C | 3 | a0001c0001t0001g0279a0001c0001t0003g0114a0001c0001t0003g0115 | 3 | HG01167.hp2 HG01169.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.856+2512T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630041 | ||||||
| chr18:630050
|
T | C | 48 | a0001c0001t0001g0068a0001c0001t0001g0078a0001c0001t0001g0081others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.856+2521T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630050 | ||||||
| chr18:630059
|
GA | G | 4 | a0001c0001t0001g0122a0001c0001t0001g0267a0001c0001t0003g0313others(1): Show | 4 | HG01243.hp1 HG03195.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+2533delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630059 | |||||
| chr18:630136
|
C | T | 407 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(404): Show | 412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.856+2607C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630136 | ||||||
| chr18:630204
|
G | C | 1 | a0001c0012t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.856+2675G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630204 | ||||||
| chr18:630234
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.856+2705G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630234 | ||||||
| chr18:630243
|
G | T | 46 | a0001c0001t0001g0068a0001c0001t0001g0078a0001c0001t0001g0081others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.856+2714G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630243 | ||||||
| chr18:630313
|
T | C | 2 | a0001c0001t0003g0345a0001c0001t0004g0132 | 2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.856+2784T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630313 | ||||||
| chr18:630361
|
G | A | 71 | a0001c0001t0001g0025a0001c0001t0001g0073a0001c0001t0001g0087others(68): Show | 71 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.856+2832G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630361 | ||||||
| chr18:630384
|
CAGGCATG others(6): Show |
C | 26 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0123others(23): Show | 26 | HG00733.hp1 HG00733.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.856+2856_856+2868d others(15): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630384 | ||||||
| chr18:630421
|
A | T | 8 | a0001c0001t0001g0049a0001c0001t0001g0122a0001c0001t0001g0209others(5): Show | 8 | HG01243.hp1 HG02717.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.857-2877A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630421 | ||||||
| chr18:630517
|
C | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | NA18986.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.857-2781C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630517 | ||||||
| chr18:630519
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | NA18986.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.857-2779G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630519 | ||||||
| chr18:630541
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.857-2757C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630541 | ||||||
| chr18:630586
|
T | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(270): Show | 276 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.857-2712T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630586 | ||||||
| chr18:630601
|
C | T | 5 | a0001c0004t0003g0344a0003c0006t0002g0127a0003c0006t0004g0317others(2): Show | 5 | HG01192.hp1 HG02055.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.857-2697C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630601 | ||||||
| chr18:630641
|
A | C | 2 | a0003c0006t0002g0127a0003c0006t0004g0317 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.857-2657A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630641 | ||||||
| chr18:630672
|
C | CT | 22 | a0001c0001t0001g0067a0001c0001t0001g0093a0001c0001t0001g0094others(19): Show | 22 | HG00741.hp2 HG01071.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.857-2593dupT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630672
|
C | CTT | 9 | a0001c0001t0001g0191a0001c0001t0001g0246a0001c0001t0001g0352others(6): Show | 9 | HG00140.hp2 HG01106.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.857-2594_857-2593d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630672
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0003g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.857-2607_857-2593d others(17): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630672
|
CT | C | 16 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0083others(13): Show | 16 | HG00323.hp2 HG00597.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.857-2593delT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630672
|
CTT | C | 49 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0078others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.857-2594_857-2593d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630672
|
CTTT | C | 55 | a0001c0001t0001g0025a0001c0001t0001g0089a0001c0001t0001g0092others(52): Show | 55 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.857-2595_857-2593d others(5): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630672
|
CTTTTTTT | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0206a0001c0001t0001g0243others(4): Show | 7 | HG00438.hp1 HG01433.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.857-2599_857-2593d others(9): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630672
|
CTTTTTTT others(1): Show |
C | 58 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0072others(55): Show | 59 | HG00423.hp2 HG00621.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.857-2600_857-2593d others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630672
|
CTTTTTTT others(2): Show |
C | 109 | a0001c0001t0001g0001a0001c0001t0001g0065a0001c0001t0001g0069others(106): Show | 110 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.857-2601_857-2593d others(11): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630672
|
CTTTTTTT others(3): Show |
C | 22 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0051others(19): Show | 23 | HG01069.hp2 HG01169.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.857-2602_857-2593d others(12): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630672
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0193 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.857-2603_857-2593d others(13): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630672
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.857-2605_857-2593d others(15): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630672
|
CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0001g0152a0001c0001t0001g0237 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.857-2614_857-2593d others(24): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630672 | |||||
| chr18:630773
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.857-2525G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630773 | ||||||
| chr18:630788
|
G | A | 79 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0072others(76): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.857-2510G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630788 | ||||||
| chr18:630796
|
C | T | 62 | a0001c0001t0001g0049a0001c0001t0001g0068a0001c0001t0001g0076others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.857-2502C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630796 | ||||||
| chr18:630812
|
G | C | 1 | a0001c0001t0002g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.857-2486G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630812 | ||||||
| chr18:630833
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0072others(81): Show | 85 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.857-2465C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630833 | ||||||
| chr18:630861
|
AT | A | 73 | a0001c0001t0001g0025a0001c0001t0001g0073a0001c0001t0001g0089others(70): Show | 73 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.857-2424delT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 630861 | |||||
| chr18:630905
|
G | T | 73 | a0001c0001t0001g0025a0001c0001t0001g0073a0001c0001t0001g0089others(70): Show | 73 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.857-2393G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630905 | ||||||
| chr18:630914
|
C | G | 65 | a0001c0001t0001g0025a0001c0001t0001g0073a0001c0001t0001g0089others(62): Show | 65 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.857-2384C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 630914 | ||||||
| chr18:631040
|
G | A | 4 | a0003c0006t0002g0127a0003c0006t0004g0317a0004c0003t0001g0075others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-2258G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631040 | ||||||
| chr18:631143
|
C | T | 2 | a0001c0001t0002g0334a0001c0001t0002g0335 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.857-2155C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631143 | ||||||
| chr18:631170
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.857-2128T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631170 | ||||||
| chr18:631211
|
T | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 251 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.857-2087T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631211 | ||||||
| chr18:631218
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.857-2080A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631218 | ||||||
| chr18:631223
|
T | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 181 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.857-2075T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631223 | ||||||
| chr18:631231
|
C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 181 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.857-2067C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631231 | ||||||
| chr18:631314
|
C | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 251 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.857-1984C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631314 | ||||||
| chr18:631332
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(239): Show | 246 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.857-1966G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631332 | ||||||
| chr18:631348
|
A | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 251 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.857-1950A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631348 | ||||||
| chr18:631367
|
C | T | 69 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0073others(66): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.857-1931C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631367 | ||||||
| chr18:631368
|
C | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 251 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.857-1930C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631368 | ||||||
| chr18:631372
|
C | CA | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 251 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.857-1926_857-1925i others(3): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631372 | ||||||
| chr18:631379
|
C | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(252): Show | 259 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.857-1919C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631379 | ||||||
| chr18:631398
|
G | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(246): Show | 253 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.857-1900G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631398 | ||||||
| chr18:631399
|
C | T | 71 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0073others(68): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.857-1899C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631399 | ||||||
| chr18:631435
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 181 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.857-1863G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631435 | ||||||
| chr18:631526
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 181 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.857-1772T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631526 | ||||||
| chr18:631994
|
G | A | 61 | a0001c0001t0001g0049a0001c0001t0001g0068a0001c0001t0001g0076others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.857-1304G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 631994 | ||||||
| chr18:632005
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0002g0045a0001c0008t0001g0350 | 3 | HG02738.hp1 HG03669.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.857-1293C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632005 | ||||||
| chr18:632006
|
A | G | 3 | a0001c0001t0001g0092a0001c0001t0002g0045a0001c0008t0001g0350 | 3 | HG02738.hp1 HG03669.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.857-1292A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632006 | ||||||
| chr18:632028
|
T | C | 1 | a0001c0001t0003g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.857-1270T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632028 | ||||||
| chr18:632233
|
C | G | 3 | a0001c0001t0001g0092a0001c0001t0002g0045a0001c0008t0001g0350 | 3 | HG02738.hp1 HG03669.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.857-1065C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632233 | ||||||
| chr18:632239
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0042others(100): Show | 105 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.857-1059T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632239 | ||||||
| chr18:632326
|
GTA | G | 5 | a0001c0001t0001g0122a0001c0001t0001g0209a0001c0001t0001g0267others(2): Show | 5 | HG01243.hp1 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.857-964_857-963del others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 632326 | |||||
| chr18:632328
|
A | C | 3 | a0001c0001t0001g0092a0001c0001t0002g0045a0001c0008t0001g0350 | 3 | HG02738.hp1 HG03669.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.857-970A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632328 | ||||||
| chr18:632334
|
A | G | 3 | a0001c0001t0001g0049a0001c0001t0001g0280a0001c0001t0004g0137 | 3 | HG02717.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.857-964A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632334 | ||||||
| chr18:632334
|
ATG | A | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(263): Show | 270 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.857-944_857-943del others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 632334 | |||||
| chr18:632354
|
GTA | G | 5 | a0001c0001t0001g0148a0001c0001t0001g0266a0001c0001t0002g0008others(2): Show | 5 | HG03041.hp1 HG03139.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.857-937_857-936del others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr18 | 632354 | |||||
| chr18:632356
|
A | G | 61 | a0001c0001t0001g0049a0001c0001t0001g0068a0001c0001t0001g0076others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.857-942A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632356 | ||||||
| chr18:632399
|
A | G | 1 | a0001c0001t0001g0352 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.857-899A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632399 | ||||||
| chr18:632620
|
A | G | 1 | a0001c0001t0003g0340 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.857-678A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632620 | ||||||
| chr18:632651
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0042others(89): Show | 94 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.857-647A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632651 | ||||||
| chr18:632749
|
C | G | 4 | a0001c0001t0001g0266a0001c0001t0002g0008a0001c0001t0002g0128others(1): Show | 4 | HG03041.hp1 HG03139.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-549C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632749 | ||||||
| chr18:632926
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.857-372G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632926 | ||||||
| chr18:632986
|
A | G | 6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0143others(3): Show | 6 | NA18962.hp2 NA18966.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.857-312A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 632986 | ||||||
| chr18:633081
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0072others(78): Show | 82 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.857-217C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 6/9 | chr18 | 633081 | ||||||
| chr18:633526
|
C | A | 1 | a0001c0001t0001g0168 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.994+91C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633526 | ||||||
| chr18:633561
|
A | C | 37 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(34): Show | 37 | HG00140.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.994+126A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633561 | ||||||
| chr18:633584
|
C | T | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0020others(1): Show | 4 | NA18953.hp2 NA18977.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+149C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633584 | ||||||
| chr18:633655
|
C | T | 84 | a0001c0001t0001g0049a0001c0001t0001g0068a0001c0001t0001g0076others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.994+220C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633655 | ||||||
| chr18:633655
|
CGCACGTG others(6): Show |
C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+223_994+235del others(13): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 633655 | |||||
| chr18:633665
|
C | T | 79 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0072others(76): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.994+230C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633665 | ||||||
| chr18:633678
|
T | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+243T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633678 | ||||||
| chr18:633680
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+245G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633680 | ||||||
| chr18:633681
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+246T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633681 | ||||||
| chr18:633682
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+247T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633682 | ||||||
| chr18:633683
|
C | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+248C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633683 | ||||||
| chr18:633687
|
TATTGGCT others(7): Show |
T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+253_994+266del others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633687 | ||||||
| chr18:633704
|
C | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+269C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633704 | ||||||
| chr18:633708
|
A | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+273A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633708 | ||||||
| chr18:633709
|
C | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+274C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633709 | ||||||
| chr18:633715
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+280A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633715 | ||||||
| chr18:633723
|
T | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+288T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633723 | ||||||
| chr18:633726
|
C | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+291C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633726 | ||||||
| chr18:633727
|
A | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+292A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633727 | ||||||
| chr18:633728
|
T | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0392 | 2 | NA18962.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.994+293T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633728 | ||||||
| chr18:633733
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+298T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633733 | ||||||
| chr18:633734
|
A | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+299A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633734 | ||||||
| chr18:633743
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+308A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633743 | ||||||
| chr18:633749
|
A | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+314A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633749 | ||||||
| chr18:633766
|
G | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+331G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633766 | ||||||
| chr18:633769
|
G | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+334G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633769 | ||||||
| chr18:633772
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+337A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633772 | ||||||
| chr18:633773
|
A | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+338A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633773 | ||||||
| chr18:633774
|
A | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+339A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633774 | ||||||
| chr18:633778
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+343G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633778 | ||||||
| chr18:633780
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+345T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633780 | ||||||
| chr18:633784
|
A | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+349A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633784 | ||||||
| chr18:633787
|
G | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+352G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633787 | ||||||
| chr18:633788
|
A | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+353A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633788 | ||||||
| chr18:633791
|
ATGTAATC others(21): Show |
A | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(192): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.994+406_994+433del others(28): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 633791 | |||||
| chr18:633791
|
ATGTAATC others(49): Show |
A | 5 | a0001c0001t0001g0159a0001c0001t0001g0298a0001c0001t0001g0299others(2): Show | 5 | HG00323.hp1 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.994+378_994+433del others(56): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 633791 | |||||
| chr18:633793
|
G | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+358G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633793 | ||||||
| chr18:633794
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+359T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633794 | ||||||
| chr18:633796
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+361A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633796 | ||||||
| chr18:633797
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+362T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633797 | ||||||
| chr18:633799
|
G | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+364G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633799 | ||||||
| chr18:633803
|
T | G | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+368T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633803 | ||||||
| chr18:633805
|
A | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+370A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633805 | ||||||
| chr18:633807
|
T | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+372T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633807 | ||||||
| chr18:633811
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+376G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633811 | ||||||
| chr18:633813
|
CGGAGCGT others(49): Show |
C | 84 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0049others(81): Show | 85 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.994+393_994+448del others(56): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 633813 | |||||
| chr18:633817
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+382G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633817 | ||||||
| chr18:633818
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.994+383C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633818 | ||||||
| chr18:633819
|
G | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+384G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633819 | ||||||
| chr18:633822
|
TAATCGGA others(69): Show |
T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+388_994+463del others(76): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633822 | ||||||
| chr18:633841
|
CGGAGCGT others(21): Show |
C | 21 | a0001c0001t0001g0122a0001c0001t0001g0178a0001c0001t0001g0266others(18): Show | 21 | HG01243.hp1 HG02055.hp1 HG02135.hp1 others(18): Show |
intron_variant | MODIFIER | c.994+421_994+448del others(28): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 633841 | |||||
| chr18:633847
|
G | A | 35 | a0001c0001t0001g0068a0001c0001t0001g0078a0001c0001t0001g0081others(32): Show | 35 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.994+412G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633847 | ||||||
| chr18:633869
|
T | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0265a0001c0001t0001g0268others(13): Show | 17 | HG01069.hp2 HG01515.hp2 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.994+434T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633869 | ||||||
| chr18:633900
|
G | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+465G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633900 | ||||||
| chr18:633901
|
A | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+466A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633901 | ||||||
| chr18:633903
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+468G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633903 | ||||||
| chr18:633907
|
T | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+472T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633907 | ||||||
| chr18:633908
|
T | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+473T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633908 | ||||||
| chr18:633919
|
G | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0049others(88): Show | 92 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.994+484G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633919 | ||||||
| chr18:633920
|
T | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+485T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633920 | ||||||
| chr18:633922
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+487G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633922 | ||||||
| chr18:633925
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+490G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633925 | ||||||
| chr18:633927
|
C | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+492C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633927 | ||||||
| chr18:633931
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+496G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633931 | ||||||
| chr18:633932
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+497A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633932 | ||||||
| chr18:633941
|
T | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+506T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633941 | ||||||
| chr18:633943
|
C | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+508C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633943 | ||||||
| chr18:633944
|
T | G | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+509T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633944 | ||||||
| chr18:633947
|
C | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+512C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633947 | ||||||
| chr18:633950
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+515A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633950 | ||||||
| chr18:633951
|
CTGATTCT others(503): Show |
C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+519_994+1028de others(1): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 633951 | |||||
| chr18:633966
|
G | T | 5 | a0001c0001t0001g0150a0001c0001t0001g0242a0001c0001t0001g0243others(2): Show | 5 | NA18955.hp2 NA18970.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.994+531G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 633966 | ||||||
| chr18:634114
|
T | C | 10 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0123others(7): Show | 10 | HG00733.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.994+679T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634114 | ||||||
| chr18:634134
|
TTTTG | T | 45 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0089others(42): Show | 46 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.994+711_994+714del others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 634134 | |||||
| chr18:634283
|
C | T | 1 | a0001c0008t0001g0350 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.994+848C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634283 | ||||||
| chr18:634412
|
A | G | 1 | a0001c0001t0004g0311 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.994+977A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634412 | ||||||
| chr18:634416
|
A | G | 1 | a0001c0001t0004g0311 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.994+981A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634416 | ||||||
| chr18:634423
|
T | C | 21 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0284others(18): Show | 21 | HG00140.hp1 HG01074.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.994+988T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634423 | ||||||
| chr18:634462
|
T | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+1027T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634462 | ||||||
| chr18:634464
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+1029T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634464 | ||||||
| chr18:634469
|
C | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+1034C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634469 | ||||||
| chr18:634478
|
T | G | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+1043T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634478 | ||||||
| chr18:634480
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+1045T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634480 | ||||||
| chr18:634484
|
A | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+1049A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634484 | ||||||
| chr18:634500
|
T | G | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+1065T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634500 | ||||||
| chr18:634503
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+1068G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634503 | ||||||
| chr18:634510
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+1075T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634510 | ||||||
| chr18:634512
|
TATGATTA others(2935): Show |
T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+1078_995-3873d others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634512 | ||||||
| chr18:634534
|
T | C | 20 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0167others(17): Show | 20 | HG00544.hp2 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.994+1099T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634534 | ||||||
| chr18:634559
|
C | A | 16 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0080others(13): Show | 16 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.994+1124C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634559 | ||||||
| chr18:634575
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0370a0001c0001t0003g0011 | 3 | HG02559.hp2 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.994+1140C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634575 | ||||||
| chr18:634665
|
A | G | 16 | a0001c0001t0001g0076a0001c0001t0001g0123a0001c0001t0001g0209others(13): Show | 16 | HG00733.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.994+1230A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634665 | ||||||
| chr18:634838
|
C | G | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0407others(2): Show | 5 | HG00280.hp2 HG01123.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.994+1403C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 634838 | ||||||
| chr18:635171
|
A | C | 4 | a0001c0001t0001g0266a0001c0001t0002g0008a0001c0001t0002g0128others(1): Show | 4 | HG03041.hp1 HG03139.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+1736A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635171 | ||||||
| chr18:635238
|
G | A | 15 | a0001c0001t0001g0076a0001c0001t0001g0080a0001c0001t0001g0123others(12): Show | 15 | HG00733.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.994+1803G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635238 | ||||||
| chr18:635288
|
G | A | 59 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0073others(56): Show | 60 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.994+1853G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635288 | ||||||
| chr18:635341
|
G | C | 5 | a0001c0001t0003g0139a0001c0001t0003g0342a0001c0001t0006g0261others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.994+1906G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635341 | ||||||
| chr18:635432
|
G | A | 29 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(26): Show | 29 | HG00140.hp1 HG00323.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.994+1997G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635432 | ||||||
| chr18:635476
|
T | A | 44 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0065others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.994+2041T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635476 | ||||||
| chr18:635604
|
A | G | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2169A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635604 | ||||||
| chr18:635637
|
G | A | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2202G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635637 | ||||||
| chr18:635667
|
C | G | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2232C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635667 | ||||||
| chr18:635673
|
C | T | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2238C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635673 | ||||||
| chr18:635685
|
C | CT | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2253dupT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 635685 | |||||
| chr18:635693
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0370 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.994+2258C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635693 | ||||||
| chr18:635714
|
G | C | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2279G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635714 | ||||||
| chr18:635730
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.994+2295C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635730 | ||||||
| chr18:635762
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.994+2327C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635762 | ||||||
| chr18:635784
|
T | C | 29 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(26): Show | 29 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.994+2349T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635784 | ||||||
| chr18:635822
|
T | C | 29 | a0001c0001t0001g0095a0001c0001t0001g0209a0001c0001t0001g0223others(26): Show | 29 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.994+2387T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635822 | ||||||
| chr18:635836
|
A | T | 29 | a0001c0001t0001g0095a0001c0001t0001g0209a0001c0001t0001g0223others(26): Show | 29 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.994+2401A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635836 | ||||||
| chr18:635839
|
C | T | 29 | a0001c0001t0001g0095a0001c0001t0001g0209a0001c0001t0001g0223others(26): Show | 29 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.994+2404C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635839 | ||||||
| chr18:635883
|
C | G | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2448C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635883 | ||||||
| chr18:635885
|
C | T | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2450C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635885 | ||||||
| chr18:635902
|
G | A | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2467G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635902 | ||||||
| chr18:635923
|
G | C | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2488G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635923 | ||||||
| chr18:635944
|
C | T | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2509C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 635944 | ||||||
| chr18:636000
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0370 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.994+2565G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636000 | ||||||
| chr18:636081
|
G | T | 1 | a0001c0001t0001g0179 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.994+2646G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636081 | ||||||
| chr18:636092
|
A | G | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2657A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636092 | ||||||
| chr18:636133
|
G | A | 64 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0073others(61): Show | 65 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.994+2698G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636133 | ||||||
| chr18:636165
|
T | C | 1 | a0001c0001t0001g0359 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.994+2730T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636165 | ||||||
| chr18:636261
|
A | G | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2826A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636261 | ||||||
| chr18:636280
|
A | G | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+2845A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636280 | ||||||
| chr18:636426
|
T | TAA | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0025others(210): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.994+2991_994+2992i others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636426 | ||||||
| chr18:636440
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.994+3005G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636440 | ||||||
| chr18:636624
|
C | CT | 20 | a0001c0001t0001g0080a0001c0001t0001g0093a0001c0001t0001g0135others(17): Show | 20 | HG00733.hp2 HG01175.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.994+3208dupT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 636624 | |||||
| chr18:636624
|
C | CTT | 73 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0068others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.994+3207_994+3208d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 636624 | |||||
| chr18:636624
|
C | CTTT | 9 | a0001c0001t0001g0084a0001c0001t0001g0142a0001c0001t0001g0170others(6): Show | 9 | HG01358.hp2 HG01361.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.994+3206_994+3208d others(5): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 636624 | |||||
| chr18:636624
|
CT | C | 105 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0042others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.994+3208delT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 636624 | |||||
| chr18:636644
|
G | C | 1 | a0001c0001t0002g0328 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.994+3209G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636644 | ||||||
| chr18:636775
|
G | A | 45 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0065others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.994+3340G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636775 | ||||||
| chr18:636786
|
C | T | 2 | a0001c0001t0002g0006a0001c0001t0003g0340 | 2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.994+3351C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636786 | ||||||
| chr18:636846
|
C | T | 32 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(29): Show | 32 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.994+3411C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636846 | ||||||
| chr18:636847
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.994+3412G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636847 | ||||||
| chr18:636855
|
G | C | 1 | a0001c0001t0004g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.994+3420G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636855 | ||||||
| chr18:636922
|
C | T | 1 | a0001c0001t0001g0405 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.994+3487C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636922 | ||||||
| chr18:636972
|
TTG | T | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+3539_994+3540d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 636972 | |||||
| chr18:636974
|
G | T | 19 | a0001c0001t0001g0049a0001c0001t0001g0066a0001c0001t0001g0076others(16): Show | 19 | HG00733.hp2 HG01109.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.994+3539G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 636974 | ||||||
| chr18:637039
|
G | T | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+3604G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637039 | ||||||
| chr18:637082
|
G | A | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+3647G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637082 | ||||||
| chr18:637106
|
C | T | 1 | a0001c0001t0003g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.994+3671C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637106 | ||||||
| chr18:637112
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.994+3677G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637112 | ||||||
| chr18:637256
|
G | A | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+3821G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637256 | ||||||
| chr18:637424
|
G | C | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.995-3903G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637424 | ||||||
| chr18:637459
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.995-3868G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637459 | ||||||
| chr18:637461
|
A | C | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.995-3866A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637461 | ||||||
| chr18:637463
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.995-3864G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637463 | ||||||
| chr18:637464
|
C | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.995-3863C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637464 | ||||||
| chr18:637466
|
G | T | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.995-3861G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637466 | ||||||
| chr18:637468
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.995-3859G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637468 | ||||||
| chr18:637469
|
T | A | 1 | a0001c0001t0002g0319 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.995-3858T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637469 | ||||||
| chr18:637631
|
C | T | 28 | a0001c0001t0001g0095a0001c0001t0001g0223a0001c0001t0001g0263others(25): Show | 28 | HG00140.hp1 HG01074.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.995-3696C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637631 | ||||||
| chr18:637655
|
C | T | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.995-3672C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637655 | ||||||
| chr18:637786
|
C | T | 44 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.995-3541C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637786 | ||||||
| chr18:637805
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0025others(139): Show | 144 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.995-3522T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637805 | ||||||
| chr18:637954
|
G | A | 44 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.995-3373G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637954 | ||||||
| chr18:637967
|
GA | G | 44 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.995-3354delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 637967 | |||||
| chr18:637974
|
T | A | 2 | a0001c0001t0001g0226a0001c0001t0001g0277 | 2 | HG00597.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.995-3353T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 637974 | ||||||
| chr18:638006
|
A | T | 2 | a0001c0001t0001g0066a0001c0001t0004g0054 | 2 | HG00733.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.995-3321A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638006 | ||||||
| chr18:638105
|
G | A | 44 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.995-3222G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638105 | ||||||
| chr18:638120
|
A | G | 1 | a0001c0008t0001g0350 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.995-3207A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638120 | ||||||
| chr18:638412
|
C | A | 1 | a0001c0008t0001g0350 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.995-2915C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638412 | ||||||
| chr18:638630
|
G | C | 44 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.995-2697G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638630 | ||||||
| chr18:638631
|
G | A | 4 | a0001c0001t0001g0080a0001c0001t0002g0126a0001c0002t0001g0270others(1): Show | 4 | HG02886.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.995-2696G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638631 | ||||||
| chr18:638681
|
A | C | 1 | a0001c0001t0001g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.995-2646A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638681 | ||||||
| chr18:638708
|
A | T | 4 | a0001c0001t0001g0168a0001c0001t0001g0206a0001c0001t0001g0406others(1): Show | 4 | HG00673.hp2 NA19011.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.995-2619A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638708 | ||||||
| chr18:638727
|
A | G | 44 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.995-2600A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638727 | ||||||
| chr18:638751
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0001g0144a0001c0001t0001g0240others(2): Show | 5 | NA18939.hp2 NA18941.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-2576C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638751 | ||||||
| chr18:638772
|
C | T | 44 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.995-2555C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638772 | ||||||
| chr18:638790
|
G | A | 45 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0080others(42): Show | 45 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.995-2537G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638790 | ||||||
| chr18:638813
|
A | G | 44 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.995-2514A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 638813 | ||||||
| chr18:638860
|
G | GAAA | 44 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.995-2457_995-2455d others(5): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 638860 | |||||
| chr18:639118
|
T | A | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.995-2209T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639118 | ||||||
| chr18:639133
|
C | T | 44 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.995-2194C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639133 | ||||||
| chr18:639142
|
TAC | T | 44 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.995-2183_995-2182d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 639142 | |||||
| chr18:639179
|
C | G | 1 | a0001c0001t0002g0320 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.995-2148C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639179 | ||||||
| chr18:639202
|
G | A | 3 | a0001c0001t0003g0139a0001c0001t0003g0342a0001c0001t0006g0261 | 3 | HG02622.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.995-2125G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639202 | ||||||
| chr18:639205
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.995-2122T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639205 | ||||||
| chr18:639341
|
G | T | 56 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0073others(53): Show | 57 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.995-1986G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639341 | ||||||
| chr18:639418
|
G | A | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.995-1909G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639418 | ||||||
| chr18:639430
|
CA | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0016others(174): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.995-1876delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 639430 | |||||
| chr18:639430
|
CAA | C | 105 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0073others(102): Show | 106 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.995-1877_995-1876d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 639430 | |||||
| chr18:639430
|
CAAAA | C | 50 | a0001c0001t0001g0004a0001c0001t0001g0068a0001c0001t0001g0078others(47): Show | 51 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.995-1879_995-1876d others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 639430 | |||||
| chr18:639471
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0287 | 2 | HG03834.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.995-1856C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639471 | ||||||
| chr18:639472
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.995-1855G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639472 | ||||||
| chr18:639537
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0280 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.995-1790G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639537 | ||||||
| chr18:639563
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.995-1764G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639563 | ||||||
| chr18:639638
|
G | A | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.995-1689G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639638 | ||||||
| chr18:639711
|
G | T | 3 | a0001c0001t0003g0139a0001c0001t0003g0342a0001c0001t0006g0261 | 3 | HG02622.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.995-1616G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639711 | ||||||
| chr18:639801
|
A | T | 1 | a0001c0001t0001g0284 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.995-1526A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639801 | ||||||
| chr18:639861
|
C | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0025others(148): Show | 153 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.995-1466C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 639861 | ||||||
| chr18:640076
|
C | T | 12 | a0001c0001t0001g0284a0001c0001t0001g0370a0001c0001t0002g0006others(9): Show | 12 | HG01361.hp1 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.995-1251C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 640076 | ||||||
| chr18:640150
|
C | A | 1 | a0001c0001t0001g0385 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.995-1177C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 640150 | ||||||
| chr18:640335
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0047others(94): Show | 99 | HG00099.hp2 HG00140.hp2 HG00673.hp2 others(96): Show |
intron_variant | MODIFIER | c.995-992A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 640335 | ||||||
| chr18:640400
|
A | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0076a0001c0001t0001g0280 | 3 | HG02630.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.995-927A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 640400 | ||||||
| chr18:640458
|
AT | A | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0025others(157): Show | 162 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.995-859delT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 640458 | |||||
| chr18:640458
|
ATT | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0092others(22): Show | 26 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.995-860_995-859del others(2): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 640458 | |||||
| chr18:640492
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0292 | 2 | HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.995-835A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 640492 | ||||||
| chr18:640544
|
A | G | 6 | a0001c0001t0001g0049a0001c0001t0001g0076a0001c0001t0001g0280others(3): Show | 6 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-783A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 640544 | ||||||
| chr18:640683
|
C | A | 2 | a0001c0004t0001g0281a0001c0004t0003g0344 | 2 | HG01192.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.995-644C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 640683 | ||||||
| chr18:640878
|
T | G | 1 | a0001c0001t0001g0160 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.995-449T>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 640878 | ||||||
| chr18:640886
|
A | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0130a0001c0001t0001g0188others(1): Show | 4 | NA18747.hp1 NA18944.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.995-441A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 640886 | ||||||
| chr18:640889
|
C | T | 2 | a0001c0001t0001g0369a0001c0001t0002g0324 | 2 | HG01496.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.995-438C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 640889 | ||||||
| chr18:640925
|
A | G | 1 | a0001c0001t0003g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.995-402A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 640925 | ||||||
| chr18:641012
|
G | A | 1 | a0001c0001t0001g0394 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.995-315G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 641012 | ||||||
| chr18:641024
|
C | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0025others(92): Show | 97 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.995-303C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 641024 | ||||||
| chr18:641058
|
G | T | 1 | a0002c0005t0001g0125 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.995-269G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 641058 | ||||||
| chr18:641084
|
A | T | 1 | a0001c0001t0001g0273 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.995-243A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 641084 | ||||||
| chr18:641126
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.995-201A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 641126 | ||||||
| chr18:641169
|
C | T | 1 | a0001c0001t0003g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.995-158C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 641169 | ||||||
| chr18:641220
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.995-107G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 7/9 | chr18 | 641220 | ||||||
| chr18:641569
|
G | A | 4 | a0001c0001t0001g0278a0001c0001t0003g0108a0001c0001t0006g0121others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209+28G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 641569 | ||||||
| chr18:641579
|
C | T | 1 | a0001c0001t0002g0128 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1209+38C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 641579 | ||||||
| chr18:641834
|
T | C | 2 | a0001c0001t0001g0278a0001c0001t0003g0108 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1209+293T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 641834 | ||||||
| chr18:641879
|
T | C | 1 | a0001c0001t0004g0141 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1209+338T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 641879 | ||||||
| chr18:641920
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1209+379G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 641920 | ||||||
| chr18:642021
|
T | C | 1 | a0001c0001t0003g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1209+480T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 642021 | ||||||
| chr18:642157
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1209+616G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 642157 | ||||||
| chr18:642263
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0047others(67): Show | 71 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1209+722T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 642263 | ||||||
| chr18:642264
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0047others(67): Show | 71 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1209+723C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 642264 | ||||||
| chr18:642307
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(228): Show | 234 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1209+766T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 642307 | ||||||
| chr18:642546
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1209+1005T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 642546 | ||||||
| chr18:642549
|
C | T | 1 | a0002c0005t0001g0125 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1209+1008C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 642549 | ||||||
| chr18:642678
|
C | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(224): Show | 230 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.1209+1137C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 642678 | ||||||
| chr18:642800
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(139): Show | 144 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1209+1259C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 642800 | ||||||
| chr18:642876
|
C | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(154): Show | 159 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1209+1335C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 642876 | ||||||
| chr18:643062
|
A | G | 17 | a0001c0001t0001g0047a0001c0001t0001g0072a0001c0001t0001g0090others(14): Show | 17 | HG00558.hp2 HG01099.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1209+1521A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 643062 | ||||||
| chr18:643131
|
CA | C | 3 | a0001c0001t0003g0342a0001c0001t0004g0140a0001c0001t0006g0261 | 3 | HG02976.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1209+1596delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr18 | 643131 | |||||
| chr18:643226
|
G | A | 2 | a0002c0005t0001g0048a0002c0005t0001g0125 | 2 | HG02109.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1210-1684G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 643226 | ||||||
| chr18:643324
|
G | T | 9 | a0001c0001t0001g0278a0001c0001t0002g0006a0001c0001t0003g0106others(6): Show | 9 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1210-1586G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 643324 | ||||||
| chr18:643711
|
T | C | 1 | a0001c0001t0002g0318 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1210-1199T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 643711 | ||||||
| chr18:643721
|
A | G | 6 | a0001c0001t0001g0066a0001c0001t0001g0210a0001c0001t0003g0107others(3): Show | 6 | HG01109.hp2 HG02922.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210-1189A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 643721 | ||||||
| chr18:643814
|
A | G | 407 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(404): Show | 412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.1210-1096A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 643814 | ||||||
| chr18:643827
|
C | T | 1 | a0002c0005t0001g0048 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1210-1083C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 643827 | ||||||
| chr18:643866
|
G | C | 5 | a0001c0001t0001g0284a0001c0001t0003g0342a0001c0001t0004g0140others(2): Show | 5 | HG02976.hp1 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210-1044G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 643866 | ||||||
| chr18:644019
|
A | C | 1 | a0001c0001t0004g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1210-891A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 644019 | ||||||
| chr18:644036
|
T | C | 2 | a0001c0001t0006g0121a0003c0006t0004g0317 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1210-874T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 644036 | ||||||
| chr18:644327
|
A | G | 6 | a0001c0001t0001g0223a0001c0001t0001g0389a0001c0001t0004g0141others(3): Show | 6 | HG02055.hp1 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1210-583A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 644327 | ||||||
| chr18:644527
|
C | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(223): Show | 229 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.1210-383C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 644527 | ||||||
| chr18:644530
|
T | C | 4 | a0001c0001t0001g0265a0001c0001t0004g0311a0001c0012t0001g0257others(1): Show | 4 | HG02258.hp2 HG02615.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210-380T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 644530 | ||||||
| chr18:644554
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1210-356C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 644554 | ||||||
| chr18:644650
|
G | C | 1 | a0001c0001t0003g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1210-260G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 644650 | ||||||
| chr18:644716
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1210-194C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 644716 | ||||||
| chr18:644734
|
A | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0047others(67): Show | 71 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1210-176A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 8/9 | chr18 | 644734 | ||||||
| chr18:645107
|
G | GTGCCTGG others(7): Show |
2 | a0002c0005t0001g0048a0002c0005t0001g0125 | 2 | HG02109.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1397+16_1397+29dup others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645107 | |||||
| chr18:645176
|
C | A | 407 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(404): Show | 412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.1397+79C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645176 | ||||||
| chr18:645262
|
TA | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0284a0001c0001t0003g0342others(3): Show | 6 | HG02976.hp1 HG03209.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1397+174delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645262 | |||||
| chr18:645303
|
T | C | 3 | a0001c0001t0004g0141a0002c0005t0001g0048a0002c0005t0001g0125 | 3 | HG02109.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1397+206T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645303 | ||||||
| chr18:645325
|
A | G | 6 | a0001c0001t0001g0278a0001c0001t0002g0006a0001c0001t0003g0106others(3): Show | 6 | HG02622.hp1 HG02723.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1397+228A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645325 | ||||||
| chr18:645517
|
C | T | 1 | a0001c0001t0002g0041 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1397+420C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645517 | ||||||
| chr18:645561
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(273): Show |
intron_variant | MODIFIER | c.1397+464T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645561 | ||||||
| chr18:645577
|
C | T | 3 | a0001c0001t0004g0141a0002c0005t0001g0048a0002c0005t0001g0125 | 3 | HG02109.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1397+480C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645577 | ||||||
| chr18:645605
|
A | C | 18 | a0001c0001t0001g0001a0001c0001t0001g0078a0001c0001t0001g0082others(15): Show | 19 | HG01975.hp1 HG01978.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.1397+508A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645605 | ||||||
| chr18:645643
|
A | G | 3 | a0001c0001t0003g0342a0001c0001t0004g0140a0001c0001t0006g0261 | 3 | HG02976.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1397+546A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645643 | ||||||
| chr18:645654
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0271a0001c0001t0001g0276 | 3 | HG02040.hp1 NA18944.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1397+557C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645654 | ||||||
| chr18:645655
|
G | A | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1397+558G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645655 | ||||||
| chr18:645666
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1397+569C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645666 | ||||||
| chr18:645667
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0052a0001c0001t0001g0065others(30): Show | 34 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1397+570G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645667 | ||||||
| chr18:645726
|
A | G | 15 | a0001c0001t0001g0042a0001c0001t0001g0149a0001c0001t0001g0151others(12): Show | 15 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.1397+629A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645726 | ||||||
| chr18:645742
|
A | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(223): Show | 229 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.1397+645A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645742 | ||||||
| chr18:645742
|
A | T | 4 | a0001c0001t0003g0342a0001c0001t0004g0140a0001c0001t0006g0261others(1): Show | 4 | HG02976.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397+645A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645742 | ||||||
| chr18:645751
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1397+654G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645751 | ||||||
| chr18:645780
|
CGA | C | 68 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0047others(65): Show | 69 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1397+686_1397+687d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645780 | |||||
| chr18:645781
|
G | A | 339 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(336): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1397+684G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645781 | ||||||
| chr18:645783
|
G | A | 68 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0047others(65): Show | 69 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1397+686G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645783 | ||||||
| chr18:645792
|
T | A | 1 | a0005c0010t0002g0018 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1397+695T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645792 | ||||||
| chr18:645792
|
T | TAA | 24 | a0001c0001t0001g0072a0001c0001t0001g0081a0001c0001t0001g0083others(21): Show | 24 | HG00558.hp2 HG01099.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.1397+713_1397+714d others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645792 | |||||
| chr18:645792
|
T | TAAA | 12 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0133others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.1397+712_1397+714d others(5): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645792 | |||||
| chr18:645792
|
T | TAAAA | 15 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0073others(12): Show | 15 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.1397+711_1397+714d others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645792 | |||||
| chr18:645792
|
T | TAAAAA | 8 | a0001c0001t0001g0223a0001c0001t0001g0229a0001c0001t0001g0275others(5): Show | 8 | HG02027.hp1 HG02074.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1397+710_1397+714d others(7): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645792 | |||||
| chr18:645792
|
T | TAAAAAA | 6 | a0001c0001t0001g0295a0001c0001t0001g0306a0001c0001t0005g0378others(3): Show | 6 | HG01516.hp2 HG01517.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397+709_1397+714d others(8): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645792 | |||||
| chr18:645792
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0006g0261 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1397+705_1397+714d others(12): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645792 | |||||
| chr18:645792
|
T | TAAAAAAA others(4): Show |
2 | a0001c0001t0001g0284a0002c0005t0001g0125 | 2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1397+704_1397+714d others(13): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645792 | |||||
| chr18:645792
|
T | TAAAAAAA others(7): Show |
1 | a0001c0001t0003g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1397+701_1397+714d others(16): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645792 | |||||
| chr18:645792
|
TA | T | 6 | a0001c0001t0002g0347a0001c0001t0003g0107a0001c0001t0003g0345others(3): Show | 6 | HG00323.hp1 HG02622.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397+714delA | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645792 | |||||
| chr18:645803
|
AAAAAAAA others(18): Show |
A | 2 | a0001c0001t0001g0278a0001c0001t0003g0108 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1397+708_1397+732d others(27): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645803 | |||||
| chr18:645804
|
AAAAAAAA others(3): Show |
A | 1 | a0007c0007t0001g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1397+709_1397+718d others(12): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645804 | |||||
| chr18:645805
|
AAAAAAAT others(24): Show |
A | 3 | a0001c0001t0001g0049a0001c0001t0001g0280a0001c0001t0002g0126 | 3 | HG02886.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1397+710_1397+740d others(33): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645805 | |||||
| chr18:645808
|
A | AAT | 7 | a0001c0001t0001g0235a0001c0001t0001g0288a0001c0001t0002g0006others(4): Show | 7 | HG02129.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1397+712_1397+713i others(4): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645808 | |||||
| chr18:645808
|
A | ATATAT | 3 | a0001c0001t0001g0124a0001c0001t0002g0010a0001c0001t0002g0022 | 3 | HG00738.hp2 NA18969.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1397+711_1397+712i others(7): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645808 | ||||||
| chr18:645808
|
A | T | 4 | a0001c0001t0001g0372a0001c0001t0003g0119a0001c0001t0003g0345others(1): Show | 4 | HG02615.hp1 HG02698.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397+711A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645808 | ||||||
| chr18:645809
|
AAATATAT others(14): Show |
A | 1 | a0001c0001t0003g0341 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1397+714_1397+734d others(23): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645809 | |||||
| chr18:645810
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0004g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1397+714_1397+715i others(18): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0002g0064a0001c0001t0004g0140 | 2 | HG01891.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1397+714_1397+715i others(17): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0086 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1397+714_1397+715i others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1397+714_1397+715i others(15): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0002g0063a0001c0001t0003g0014 | 2 | HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1397+714_1397+715i others(12): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0160 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1397+714_1397+715i others(12): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1397+714_1397+715i others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1397+714_1397+715i others(16): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
A | AAAATAT | 9 | a0001c0001t0001g0050a0001c0001t0001g0093a0001c0001t0001g0097others(6): Show | 9 | HG00735.hp1 HG01928.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1397+714_1397+715i others(8): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
A | AAATAT | 9 | a0001c0001t0001g0080a0001c0001t0001g0250a0001c0001t0001g0253others(6): Show | 9 | HG01243.hp2 HG01358.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.1397+714_1397+715i others(7): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
A | AATAT | 8 | a0001c0001t0001g0052a0001c0001t0001g0074a0001c0001t0001g0283others(5): Show | 8 | HG00609.hp1 HG01255.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1397+752_1397+755d others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
A | AATATAT | 7 | a0001c0001t0001g0004a0001c0001t0001g0189a0001c0001t0001g0381others(4): Show | 8 | HG00140.hp1 HG00140.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1397+750_1397+755d others(8): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
A | AT | 6 | a0001c0001t0001g0183a0001c0001t0001g0254a0001c0001t0001g0277others(3): Show | 6 | HG00733.hp2 HG03491.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.1397+713_1397+714i others(3): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645810 | ||||||
| chr18:645810
|
A | ATAT | 12 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0001g0221others(9): Show | 12 | HG00280.hp2 HG01123.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.1397+713_1397+714i others(5): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645810 | ||||||
| chr18:645810
|
A | ATATAT | 11 | a0001c0001t0001g0122a0001c0001t0001g0163a0001c0001t0001g0199others(8): Show | 11 | HG00639.hp2 HG01074.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1397+713_1397+714i others(7): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645810 | ||||||
| chr18:645810
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0020 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1397+713_1397+714i others(13): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645810 | ||||||
| chr18:645810
|
A | T | 27 | a0001c0001t0001g0124a0001c0001t0001g0224a0001c0001t0001g0225others(24): Show | 27 | HG00738.hp2 HG01192.hp1 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.1397+713A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645810 | ||||||
| chr18:645810
|
AATATATA others(5): Show |
A | 21 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0152others(18): Show | 21 | HG00408.hp1 HG01106.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1397+744_1397+755d others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
AATATATA others(7): Show |
A | 52 | a0001c0001t0001g0001a0001c0001t0001g0042a0001c0001t0001g0067others(49): Show | 53 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1397+742_1397+755d others(16): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
AATATATA others(9): Show |
A | 2 | a0001c0001t0002g0100a0001c0001t0003g0313 | 2 | HG01106.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1397+740_1397+755d others(18): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
AATATATA others(11): Show |
A | 2 | a0001c0001t0004g0141a0002c0005t0001g0048 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1397+738_1397+755d others(20): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
AATATATA others(13): Show |
A | 4 | a0001c0001t0001g0268a0001c0001t0001g0382a0001c0001t0002g0318others(1): Show | 4 | HG01074.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397+736_1397+755d others(22): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645810
|
AATATATA others(17): Show |
A | 2 | a0001c0001t0001g0302a0001c0001t0009g0218 | 2 | NA19010.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1397+732_1397+755d others(26): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 645810 | |||||
| chr18:645811
|
ATATAT | A | 3 | a0001c0001t0001g0273a0001c0001t0001g0390a0001c0001t0003g0322 | 3 | HG00423.hp2 NA18994.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1397+715_1397+719d others(7): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645811 | ||||||
| chr18:645811
|
ATATATAT others(4): Show |
A | 7 | a0001c0001t0001g0220a0001c0001t0001g0236a0001c0001t0001g0242others(4): Show | 7 | HG00597.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1397+715_1397+725d others(13): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645811 | ||||||
| chr18:645811
|
ATATATAT others(6): Show |
A | 53 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(50): Show | 54 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1397+715_1397+727d others(15): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645811 | ||||||
| chr18:645811
|
ATATATAT others(8): Show |
A | 8 | a0001c0001t0001g0095a0001c0001t0001g0204a0001c0001t0001g0209others(5): Show | 8 | HG01243.hp1 HG02486.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1397+715_1397+729d others(17): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645811 | ||||||
| chr18:645811
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1397+715_1397+733d others(21): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645811 | ||||||
| chr18:645812
|
T | A | 60 | a0001c0001t0001g0025a0001c0001t0001g0072a0001c0001t0001g0073others(57): Show | 60 | HG00280.hp1 HG00558.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1397+715T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645812 | ||||||
| chr18:645814
|
T | A | 50 | a0001c0001t0001g0025a0001c0001t0001g0072a0001c0001t0001g0073others(47): Show | 50 | HG00280.hp1 HG00558.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1397+717T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645814 | ||||||
| chr18:645816
|
T | A | 34 | a0001c0001t0001g0025a0001c0001t0001g0072a0001c0001t0001g0090others(31): Show | 34 | HG00280.hp1 HG00558.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1397+719T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645816 | ||||||
| chr18:645818
|
T | A | 24 | a0001c0001t0001g0072a0001c0001t0001g0090a0001c0001t0001g0145others(21): Show | 24 | HG00280.hp1 HG00558.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1397+721T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645818 | ||||||
| chr18:645820
|
T | A | 15 | a0001c0001t0001g0090a0001c0001t0001g0145a0001c0001t0001g0159others(12): Show | 15 | HG00280.hp1 HG00558.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.1397+723T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645820 | ||||||
| chr18:645822
|
T | A | 8 | a0001c0001t0001g0145a0001c0001t0001g0159a0001c0001t0001g0171others(5): Show | 8 | HG00558.hp2 HG04204.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.1397+725T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645822 | ||||||
| chr18:645824
|
T | A | 29 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0152others(26): Show | 29 | HG00408.hp1 HG00597.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1397+727T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645824 | ||||||
| chr18:645826
|
T | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(130): Show | 135 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1397+729T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645826 | ||||||
| chr18:645828
|
T | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(140): Show | 145 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1397+731T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645828 | ||||||
| chr18:645830
|
T | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(141): Show | 146 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1397+733T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645830 | ||||||
| chr18:645832
|
T | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(134): Show | 139 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1397+735T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645832 | ||||||
| chr18:645834
|
T | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(97): Show | 101 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1397+737T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645834 | ||||||
| chr18:645836
|
T | A | 12 | a0001c0001t0001g0276a0001c0001t0001g0279a0001c0001t0001g0368others(9): Show | 12 | HG02280.hp1 HG02486.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1397+739T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645836 | ||||||
| chr18:645838
|
T | A | 3 | a0001c0001t0001g0368a0001c0001t0001g0405a0001c0001t0004g0138 | 3 | HG02280.hp1 HG02486.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1397+741T>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645838 | ||||||
| chr18:645839
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1397+742A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645839 | ||||||
| chr18:645852
|
T | C | 2 | a0001c0001t0003g0114a0001c0001t0003g0115 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1397+755T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645852 | ||||||
| chr18:645878
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0277 | 2 | HG00621.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1397+781A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645878 | ||||||
| chr18:645947
|
C | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(223): Show | 229 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.1397+850C>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 645947 | ||||||
| chr18:646026
|
CATG | C | 3 | a0001c0001t0001g0223a0001c0001t0001g0389a0001c0004t0001g0281 | 3 | HG02630.hp2 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1397+932_1397+934d others(5): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646026 | |||||
| chr18:646053
|
G | A | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0143others(4): Show | 7 | NA18962.hp2 NA18966.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.1397+956G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646053 | ||||||
| chr18:646087
|
C | T | 1 | a0001c0011t0001g0071 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1397+990C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646087 | ||||||
| chr18:646095
|
G | A | 1 | a0001c0001t0003g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1397+998G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646095 | ||||||
| chr18:646147
|
C | T | 2 | a0001c0001t0001g0284a0001c0011t0001g0071 | 2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1397+1050C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646147 | ||||||
| chr18:646159
|
A | G | 1 | a0001c0001t0001g0376 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1397+1062A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646159 | ||||||
| chr18:646323
|
A | T | 1 | a0001c0001t0001g0296 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1397+1226A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646323 | ||||||
| chr18:646487
|
CAGAT | C | 6 | a0001c0001t0001g0066a0001c0001t0001g0210a0001c0001t0003g0107others(3): Show | 6 | HG01109.hp2 HG02922.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1397+1398_1397+140 others(8): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646487 | |||||
| chr18:646493
|
GATAGAC | G | 3 | a0001c0001t0003g0342a0001c0001t0004g0140a0001c0001t0006g0261 | 3 | HG02976.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1397+1398_1397+140 others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646493 | |||||
| chr18:646493
|
GATAGACA others(1): Show |
G | 3 | a0001c0001t0001g0223a0001c0001t0001g0389a0001c0004t0001g0281 | 3 | HG02630.hp2 HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1397+1398_1397+140 others(12): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646493 | |||||
| chr18:646497
|
G | GAC | 67 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0050others(64): Show | 68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.1397+1441_1397+144 others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646497 | |||||
| chr18:646497
|
G | GACAC | 17 | a0001c0001t0001g0065a0001c0001t0001g0183a0001c0001t0001g0211others(14): Show | 17 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1397+1439_1397+144 others(8): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646497 | |||||
| chr18:646497
|
G | GACACAC | 27 | a0001c0001t0001g0003a0001c0001t0001g0074a0001c0001t0001g0097others(24): Show | 28 | HG00639.hp2 HG01167.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1397+1437_1397+144 others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646497 | |||||
| chr18:646497
|
G | GACACACA others(1): Show |
7 | a0001c0001t0001g0073a0001c0001t0001g0231a0001c0001t0001g0232others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1397+1435_1397+144 others(12): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646497 | |||||
| chr18:646497
|
G | GACACACA others(3): Show |
4 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0391others(1): Show | 4 | HG01109.hp1 NA18954.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397+1433_1397+144 others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646497 | |||||
| chr18:646497
|
GAC | G | 70 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0072others(67): Show | 70 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1397+1441_1397+144 others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646497 | |||||
| chr18:646497
|
GACAC | G | 17 | a0001c0001t0001g0090a0001c0001t0001g0124a0001c0001t0001g0145others(14): Show | 17 | HG00558.hp2 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1397+1439_1397+144 others(8): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646497 | |||||
| chr18:646497
|
GACACAC | G | 19 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0080others(16): Show | 19 | HG00673.hp2 HG01074.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1397+1437_1397+144 others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646497 | |||||
| chr18:646497
|
GACACACA others(1): Show |
G | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(127): Show | 132 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1397+1435_1397+144 others(12): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646497 | |||||
| chr18:646497
|
GACACACA others(3): Show |
G | 4 | a0001c0001t0002g0035a0002c0005t0001g0048a0002c0005t0001g0125others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397+1433_1397+144 others(14): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646497 | |||||
| chr18:646497
|
GACACACA others(5): Show |
G | 1 | a0001c0001t0003g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1397+1431_1397+144 others(16): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 646497 | |||||
| chr18:646681
|
C | G | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1397+1584C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646681 | ||||||
| chr18:646710
|
C | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0267a0001c0001t0002g0100others(1): Show | 4 | HG01106.hp1 HG01243.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397+1613C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646710 | ||||||
| chr18:646748
|
C | T | 5 | a0001c0001t0001g0290a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1397+1651C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646748 | ||||||
| chr18:646834
|
C | T | 3 | a0001c0001t0003g0119a0001c0001t0006g0121a0003c0006t0004g0317 | 3 | HG02615.hp1 HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1397+1737C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646834 | ||||||
| chr18:646843
|
A | G | 1 | a0001c0001t0001g0367 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1397+1746A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646843 | ||||||
| chr18:646895
|
G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0047others(68): Show | 72 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1397+1798G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646895 | ||||||
| chr18:646907
|
GCC | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0168a0006c0009t0002g0015 | 3 | NA18957.hp1 NA18968.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1397+1811_1397+181 others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 646907 | ||||||
| chr18:647006
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0003g0342a0001c0001t0006g0261 | 3 | HG03209.hp2 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1397+1909C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647006 | ||||||
| chr18:647052
|
C | G | 1 | a0001c0001t0001g0284 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1397+1955C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647052 | ||||||
| chr18:647155
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0002g0329 | 2 | NA18949.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1397+2058G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647155 | ||||||
| chr18:647156
|
G | T | 34 | a0001c0001t0001g0047a0001c0001t0001g0072a0001c0001t0001g0090others(31): Show | 34 | HG00408.hp2 HG00558.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1397+2059G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647156 | ||||||
| chr18:647171
|
C | CAAATACG others(52): Show |
5 | a0001c0001t0001g0003a0001c0001t0001g0087a0001c0001t0001g0169others(2): Show | 6 | HG00323.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1397+2135_1397+219 others(63): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 647171 | |||||
| chr18:647171
|
C | CAAATACG others(170): Show |
1 | a0001c0001t0001g0283 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1397+2193_1397+219 others(181): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 647171 | |||||
| chr18:647171
|
CAAATACG others(52): Show |
C | 13 | a0001c0001t0001g0005a0001c0001t0001g0072a0001c0001t0001g0143others(10): Show | 14 | HG00438.hp1 HG01074.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.1397+2135_1397+219 others(63): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 647171 | |||||
| chr18:647178
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1397+2081G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647178 | ||||||
| chr18:647206
|
T | C | 2 | a0001c0001t0006g0121a0003c0006t0004g0317 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1397+2109T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647206 | ||||||
| chr18:647232
|
A | G | 4 | a0001c0001t0003g0107a0001c0001t0003g0345a0001c0002t0001g0270others(1): Show | 4 | HG02922.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397+2135A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647232 | ||||||
| chr18:647268
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | NA18948.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1397+2171G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647268 | ||||||
| chr18:647388
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0047others(67): Show | 71 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1397+2291C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647388 | ||||||
| chr18:647513
|
G | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(125): Show | 130 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1398-2385G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647513 | ||||||
| chr18:647772
|
A | C | 11 | a0001c0001t0001g0052a0001c0001t0001g0065a0001c0001t0001g0300others(8): Show | 11 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1398-2126A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647772 | ||||||
| chr18:647846
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(125): Show | 130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1398-2052T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647846 | ||||||
| chr18:647891
|
C | G | 1 | a0001c0001t0003g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1398-2007C>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647891 | ||||||
| chr18:647954
|
G | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0215a0001c0001t0001g0220others(2): Show | 5 | HG00558.hp1 HG00597.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1398-1944G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647954 | ||||||
| chr18:647961
|
G | C | 68 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0072others(65): Show | 69 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1398-1937G>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 647961 | ||||||
| chr18:648232
|
A | C | 1 | a0001c0001t0001g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1398-1666A>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 648232 | ||||||
| chr18:648356
|
T | C | 68 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0072others(65): Show | 69 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1398-1542T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 648356 | ||||||
| chr18:648370
|
AATGTTT | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0267a0001c0001t0002g0100others(1): Show | 4 | HG01106.hp1 HG01243.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-1527_1398-152 others(10): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 648370 | ||||||
| chr18:648412
|
C | T | 1 | a0001c0001t0004g0060 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1398-1486C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 648412 | ||||||
| chr18:648465
|
A | G | 74 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0072others(71): Show | 75 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1398-1433A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 648465 | ||||||
| chr18:648542
|
A | T | 2 | a0001c0011t0001g0071a0002c0005t0001g0125 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1398-1356A>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 648542 | ||||||
| chr18:648581
|
G | GAT | 10 | a0001c0001t0001g0092a0001c0001t0001g0364a0001c0001t0001g0401others(7): Show | 10 | HG00140.hp1 HG02055.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1398-1301_1398-130 others(6): Show |
CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 648581 | |||||
| chr18:648857
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1398-1041C>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 648857 | ||||||
| chr18:648867
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1398-1031G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 648867 | ||||||
| chr18:649024
|
G | T | 1 | a0001c0001t0002g0329 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1398-874G>T | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 649024 | ||||||
| chr18:649311
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1398-587A>G | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 649311 | ||||||
| chr18:649355
|
G | A | 1 | a0001c0001t0001g0359 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1398-543G>A | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 649355 | ||||||
| chr18:649759
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0049others(97): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.1398-139T>C | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | chr18 | 649759 | ||||||
| chr18:649879
|
CT | C | 21 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0080others(18): Show | 23 | HG01256.hp2 HG01258.hp1 HG01515.hp2 others(20): Show |
splice_region_variant&intron_variant | LOW | c.1398-4delT | CLUL1 | ENSG00000079101.18 | transcript | ENST00000692774.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 649879 |